The Virginia Register OF
REGULATIONS is an official state publication issued every other week
throughout the year. Indexes are published quarterly, and are cumulative for
the year. The Virginia Register has several functions. The new and
amended sections of regulations, both as proposed and as finally adopted, are
required by law to be published in the Virginia Register. In addition,
the Virginia Register is a source of other information about state
government, including petitions for rulemaking, emergency regulations,
executive orders issued by the Governor, and notices of public hearings on
regulations.
ADOPTION,
AMENDMENT, AND REPEAL OF REGULATIONS
An
agency wishing to adopt, amend, or repeal regulations must first publish in the
Virginia Register a notice of intended regulatory action; a basis,
purpose, substance and issues statement; an economic impact analysis prepared
by the Department of Planning and Budget; the agency’s response to the economic
impact analysis; a summary; a notice giving the public an opportunity to
comment on the proposal; and the text of the proposed regulation.
Following
publication of the proposal in the Virginia Register, the promulgating agency
receives public comments for a minimum of 60 days. The Governor reviews the
proposed regulation to determine if it is necessary to protect the public
health, safety and welfare, and if it is clearly written and easily
understandable. If the Governor chooses to comment on the proposed regulation,
his comments must be transmitted to the agency and the Registrar no later than
15 days following the completion of the 60-day public comment period. The
Governor’s comments, if any, will be published in the Virginia Register.
Not less than 15 days following the completion of the 60-day public comment
period, the agency may adopt the proposed regulation.
The
Joint Commission on Administrative Rules (JCAR) or the appropriate standing
committee of each house of the General Assembly may meet during the
promulgation or final adoption process and file an objection with the Registrar
and the promulgating agency. The objection will be published in the Virginia
Register. Within 21 days after receipt by the agency of a legislative
objection, the agency shall file a response with the Registrar, the objecting
legislative body, and the Governor.
When
final action is taken, the agency again publishes the text of the regulation as
adopted, highlighting all changes made to the proposed regulation and
explaining any substantial changes made since publication of the proposal. A
30-day final adoption period begins upon final publication in the Virginia
Register.
The
Governor may review the final regulation during this time and, if he objects,
forward his objection to the Registrar and the agency. In addition to or in
lieu of filing a formal objection, the Governor may suspend the effective date
of a portion or all of a regulation until the end of the next regular General
Assembly session by issuing a directive signed by a majority of the members of
the appropriate legislative body and the Governor. The Governor’s objection or
suspension of the regulation, or both, will be published in the Virginia
Register. If the Governor finds that changes made to the proposed
regulation have substantial impact, he may require the agency to provide an
additional 30-day public comment period on the changes. Notice of the
additional public comment period required by the Governor will be published in
the Virginia Register.
The
agency shall suspend the regulatory process for 30 days when it receives
requests from 25 or more individuals to solicit additional public comment,
unless the agency determines that the changes have minor or inconsequential
impact.
A
regulation becomes effective at the conclusion of the 30-day final adoption
period, or at any other later date specified by the promulgating agency, unless
(i) a legislative objection has been filed, in which event the regulation,
unless withdrawn, becomes effective on the date specified, which shall be after
the expiration of the 21-day objection period; (ii) the Governor exercises his
authority to require the agency to provide for additional public comment, in
which event the regulation, unless withdrawn, becomes effective on the date
specified, which shall be after the expiration of the period for which the
Governor has provided for additional public comment; (iii) the Governor and the
General Assembly exercise their authority to suspend the effective date of a
regulation until the end of the next regular legislative session; or (iv) the
agency suspends the regulatory process, in which event the regulation, unless
withdrawn, becomes effective on the date specified, which shall be after the
expiration of the 30-day public comment period and no earlier than 15 days from
publication of the readopted action.
A
regulatory action may be withdrawn by the promulgating agency at any time
before the regulation becomes final.
FAST-TRACK
RULEMAKING PROCESS
Section
2.2-4012.1 of the Code of Virginia provides an exemption from certain
provisions of the Administrative Process Act for agency regulations deemed by
the Governor to be noncontroversial. To use this process, Governor's
concurrence is required and advance notice must be provided to certain
legislative committees. Fast-track regulations will become effective on the
date noted in the regulatory action if no objections to using the process are
filed in accordance with § 2.2-4012.1.
EMERGENCY
REGULATIONS
Pursuant
to § 2.2-4011 of the Code of Virginia, an agency, upon consultation
with the Attorney General, and at the discretion of the Governor, may adopt
emergency regulations that are necessitated by an emergency situation. An
agency may also adopt an emergency regulation when Virginia statutory law or
the appropriation act or federal law or federal regulation requires that a
regulation be effective in 280 days or less from its enactment. The emergency regulation becomes operative upon its
adoption and filing with the Registrar of Regulations, unless a later date is
specified. Emergency regulations are limited to no more than 18 months in
duration; however, may be extended for six months under certain circumstances
as provided for in § 2.2-4011 D. Emergency regulations are published as
soon as possible in the Register.
During
the time the emergency status is in effect, the agency may proceed with the
adoption of permanent regulations through the usual procedures. To begin
promulgating the replacement regulation, the agency must (i) file the Notice of
Intended Regulatory Action with the Registrar within 60 days of the effective
date of the emergency regulation and (ii) file the proposed regulation with the
Registrar within 180 days of the effective date of the emergency regulation. If
the agency chooses not to adopt the regulations, the emergency status ends when
the prescribed time limit expires.
STATEMENT
The
foregoing constitutes a generalized statement of the procedures to be followed.
For specific statutory language, it is suggested that Article 2 (§ 2.2-4006
et seq.) of Chapter 40 of Title 2.2 of the Code of Virginia be examined
carefully.
CITATION
TO THE VIRGINIA REGISTER
The Virginia
Register is cited by volume, issue, page number, and date. 29:5 VA.R. 1075-1192
November 5, 2012, refers to Volume 29, Issue 5, pages 1075 through 1192 of
the Virginia Register issued on
November 5, 2012.
The
Virginia Register of Regulations is
published pursuant to Article 6 (§ 2.2-4031 et seq.) of Chapter 40 of Title 2.2
of the Code of Virginia.
Members
of the Virginia Code Commission: John
S. Edwards, Chair; James M. LeMunyon, Vice Chair; Gregory D.
Habeeb; Ryan T. McDougle; Pamela S. Baskervill; Robert L.
Calhoun; Carlos L. Hopkins; E.M. Miller, Jr.; Thomas M. Moncure, Jr.; Christopher
R. Nolen; Timothy Oksman; Charles S. Sharp; Mark J. Vucci.
Staff
of the Virginia Register: Jane
D. Chaffin, Registrar of Regulations; Karen Perrine, Assistant
Registrar; Anne Bloomsburg, Regulations Analyst; Rhonda Dyer, Publications
Assistant; Terri Edwards, Operations Staff Assistant.
PUBLICATION SCHEDULE AND DEADLINES
Vol. 32 Iss. 23 - July 11, 2016
July 2016 through July 2017
Volume: Issue
|
Material Submitted By Noon*
|
Will Be Published On
|
32:23
|
June 22, 2016
|
July 11, 2016
|
32:24
|
July 6, 2016
|
July 25, 2016
|
32:25
|
July 20, 2016
|
August 8, 2016
|
32:26
|
August 3, 2016
|
August 22, 2016
|
33:1
|
August 17, 2016
|
September 5, 2016
|
33:2
|
August 31, 2016
|
September 19, 2016
|
33:3
|
September 14, 2016
|
October 3, 2016
|
33:4
|
September 28, 2016
|
October 17, 2016
|
33:5
|
October 12, 2016
|
October 31, 2016
|
33:6
|
October 26, 2016
|
November 14, 2016
|
33:7
|
November 9, 2016
|
November 28, 2016
|
33:8
|
November 22, 2016 (Tuesday)
|
December 12, 2016
|
33:9
|
December 7, 2016
|
December 26, 2016
|
33:10
|
December 19, 2016 (Monday)
|
January 9, 2017
|
33:11
|
January 4, 2017
|
January 23, 2017
|
33:12
|
January 18, 2017
|
February 6, 2017
|
33:13
|
February 1, 2017
|
February 20, 2017
|
33:14
|
February 15, 2017
|
March 6, 2017
|
33:15
|
March 1, 2017
|
March 20, 2017
|
33:16
|
March 15, 2017
|
April 3, 2017
|
33:17
|
March 29, 2017
|
April 17, 2017
|
33:18
|
April 12, 2017
|
May 1, 2017
|
33:19
|
April 26, 2017
|
May 15, 2017
|
33:20
|
May 10, 2017
|
May 29, 2017
|
33:21
|
May 24, 2017
|
June 12, 2017
|
33:22
|
June 7, 2017
|
June 26, 2017
|
33:23
|
June 21, 2017
|
July 10, 2017
|
*Filing deadlines are Wednesdays
unless otherwise specified.
NOTICES OF INTENDED REGULATORY ACTION
Vol. 32 Iss. 23 - July 11, 2016
TITLE 9. ENVIRONMENT
General VPDES Permit for Discharges of Stormwater from Small Municipal Separate Storm Sewer Systems
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the State Water Control Board intends to consider
amending 9VAC25-890, General VPDES Permit for Discharges of Stormwater from
Small Municipal Separate Storm Sewer Systems. The purpose of the proposed
action is to amend and reissue the existing general permit, which expires on
June 30, 2018. The general permit governs local governments, state agencies,
and federal agencies that discharge stormwater from municipally owned separate
storm sewer systems located within "urbanized areas" as designated by
the U.S. Census Bureau.
In addition, pursuant to Executive Order 17 (2014) and
§ 2.2-4007.1 of the Code of Virginia, the agency is conducting a periodic
review and small business impact review of this regulation to determine whether
this regulation should be terminated, amended, or retained in its current form.
Public comment is sought on the review of any issue relating to this
regulation, including whether the regulation (i) is necessary for the
protection of public health, safety, and welfare or for the economical
performance of important governmental functions; (ii) minimizes the economic
impact on small businesses in a manner consistent with the stated objectives of
applicable law; (iii) is designed to achieve its intended objective in the most
efficient, cost-effective manner; (iv) is clearly written and easily understandable;
and (v) overlaps, duplicates, or conflicts with federal or state law or
regulation. Additional consideration will be given to the degree to which
technology, economic conditions, or other factors have changed in the area
affected by the regulation since the last review.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: § 62.1-44.15:28 of the Code of
Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Jaime Bauer, Department of Environmental
Quality, 629 East Main Street, P.O. Box 1105, Richmond, VA 23218, telephone
(804) 698-4416, FAX (804) 698-5106, or email jaime.bauer@deq.virginia.gov.
VA.R. Doc. No. R16-4777; Filed June 22, 2016, 7:47 a.m.
TITLE 12. HEALTH
Standards Established and Methods Used to Assure High Quality Care
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Medical Assistance Services intends to
consider amending 12VAC30-60, Standards Established and Methods Used to
Assure High Quality Care. The purpose of the proposed action is to
implement Chapter 413 of the 2014 Acts of Assembly, Item 301 QQQQ of Chapter 3
of the 2015 Acts of Assembly, and Item 306 PPP of Chapter 780 of the 2016 Acts
of Assembly and to improve the preadmission screening process for individuals who
will be eligible for long-term services and supports. The regulatory action may
include (i) adding requirements for accepting screening requests, managing the
screening process, and submitting findings from screenings completed by
community and hospital preadmission screening (PAS) teams and contractors
performing screenings; (ii) use of the electronic preadmission screening (ePAS)
system; (iii) contracting with public or private entities to perform screenings
that have not been completed within 30 days of an individual's request; (iv)
contracting out community based screenings for children; (v) clarifying
requirements of community and hospital PAS teams and screenings performed by
these teams; and (vi) adding a definitions section.
The agency does not intend to hold a public hearing on the
proposed action after publication in the Virginia Register.
Statutory Authority: § 32.1-325 of the Code of
Virginia; 42 USC § 1396 et seq.
Public Comment Deadline: August 10, 2016.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, Policy Division, 600 East Broad
Street, Suite 1300, Richmond, VA 23219, telephone (804) 371-4300, FAX (804)
786-1680, or email emily.mcclellan@dmas.virginia.gov.
VA.R. Doc. No. R16-4355; Filed June 21, 2016, 10:25 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
Regulations Governing the Certification of Massage Therapists
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Nursing intends to consider amending 18VAC90-50,
Regulations Governing the Certification of Massage Therapists, as a result
of the periodic review of regulations conducted by the board. The purpose of
the proposed action is to clarify certain sections, offer additional options
for completion of continuing education, require an attestation of compliance
with laws and ethics for initial certification, and add provisions to the
standards of conduct that may subject a regulant to disciplinary action. The
Board of Nursing will initiate a separate regulatory action to amend the
regulation in accordance with Chapter 324 of the 2016 Acts of Assembly, which
requires that massage therapists be licensed, rather than certified.
This Notice of Intended Regulatory Action serves as the report
of the findings of the regulatory review pursuant to § 2.2-4007.1 of the
Code of Virginia.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: §§ 54.1 2400 and 54.1-3005 of the
Code of Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Jay P. Douglas, R.N., Executive
Director, Board of Nursing, 9960 Mayland Drive, Suite 300, Richmond, VA
23233-1463, telephone (804) 367-4515, FAX (804) 527-4455, or email
jay.douglas@dhp.virginia.gov.
VA.R. Doc. No. R16-4739; Filed June 18, 2016, 11:19 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
Regulations Governing the Delegation of Informal Fact-Finding Proceedings to an Agency Subordinate
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Pharmacy intends to consider (i) amending 18VAC110-20,
Regulations Governing the Practice of Pharmacy, and 18VAC110-50,
Regulations Governing Wholesale Distributors, Manufacturers, and Warehousers
and (ii) adopting 18VAC110-16, Regulations Governing the Delegation of
Informal Fact-Finding Proceedings to an Agency Subordinate, and
18VAC110-25, Regulations Governing the Licensure of Pharmacists and
Registration of Pharmacy Technicians. The purpose of the proposed action is
to (i) reduce the size and complexity of 18VAC110-20 by moving some of the
provisions of that chapter into new chapters and (ii) amend 18VAC110-20 and
18VAC110-50 to clarify certain requirements, incorporate provisions currently
found in guidance documents, and update and streamline requirements where
possible. Provisions relating to the licensure of pharmacists and registration
of pharmacy technicians and certain general provisions will be moved from
18VAC110-20 to new chapter 18VAC110-25. Additionally, 18VAC110-20-15, relating
to criteria for delegation of informal fact-finding proceedings to an agency
subordinate, will be moved into new chapter 18VAC110-16 because it applies to
all types of licensees, registrants, and permit holders regulated by the board.
The regulatory action being considered is in response to a
periodic review of the regulations, and this Notice of Intended Regulatory
Action serves as the report of the findings of the regulatory review pursuant
to § 2.2-4007.1 of the Code of Virginia.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: §§ 54.1-2400 and 54.1-3307 of the
Code of Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Caroline Juran, RPh, Executive Director,
Board of Pharmacy, 9960 Mayland Drive, Suite 300, Richmond, VA 23233-1463,
telephone (804) 367-4416, FAX (804) 527-4472, or email
caroline.juran@dhp.virginia.gov.
VA.R. Doc. No. R16-4673; Filed June 18, 2016, 11:20 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
Regulations Governing the Practice of Pharmacy
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Pharmacy intends to consider (i) amending 18VAC110-20,
Regulations Governing the Practice of Pharmacy, and 18VAC110-50,
Regulations Governing Wholesale Distributors, Manufacturers, and Warehousers
and (ii) adopting 18VAC110-16, Regulations Governing the Delegation of
Informal Fact-Finding Proceedings to an Agency Subordinate, and
18VAC110-25, Regulations Governing the Licensure of Pharmacists and
Registration of Pharmacy Technicians. The purpose of the proposed action is
to (i) reduce the size and complexity of 18VAC110-20 by moving some of the
provisions of that chapter into new chapters and (ii) amend 18VAC110-20 and
18VAC110-50 to clarify certain requirements, incorporate provisions currently
found in guidance documents, and update and streamline requirements where
possible. Provisions relating to the licensure of pharmacists and registration
of pharmacy technicians and certain general provisions will be moved from
18VAC110-20 to new chapter 18VAC110-25. Additionally, 18VAC110-20-15, relating
to criteria for delegation of informal fact-finding proceedings to an agency
subordinate, will be moved into new chapter 18VAC110-16 because it applies to
all types of licensees, registrants, and permit holders regulated by the board.
The regulatory action being considered is in response to a
periodic review of the regulations, and this Notice of Intended Regulatory
Action serves as the report of the findings of the regulatory review pursuant
to § 2.2-4007.1 of the Code of Virginia.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: §§ 54.1-2400 and 54.1-3307 of the
Code of Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Caroline Juran, RPh, Executive Director,
Board of Pharmacy, 9960 Mayland Drive, Suite 300, Richmond, VA 23233-1463,
telephone (804) 367-4416, FAX (804) 527-4472, or email
caroline.juran@dhp.virginia.gov.
VA.R. Doc. No. R16-4673; Filed June 18, 2016, 11:20 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
Regulations Governing the Licensure of Pharmacists and Registration of Pharmacy Technicians
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Pharmacy intends to consider (i) amending 18VAC110-20,
Regulations Governing the Practice of Pharmacy, and 18VAC110-50,
Regulations Governing Wholesale Distributors, Manufacturers, and Warehousers
and (ii) adopting 18VAC110-16, Regulations Governing the Delegation of
Informal Fact-Finding Proceedings to an Agency Subordinate, and
18VAC110-25, Regulations Governing the Licensure of Pharmacists and
Registration of Pharmacy Technicians. The purpose of the proposed action is
to (i) reduce the size and complexity of 18VAC110-20 by moving some of the
provisions of that chapter into new chapters and (ii) amend 18VAC110-20 and
18VAC110-50 to clarify certain requirements, incorporate provisions currently
found in guidance documents, and update and streamline requirements where
possible. Provisions relating to the licensure of pharmacists and registration
of pharmacy technicians and certain general provisions will be moved from
18VAC110-20 to new chapter 18VAC110-25. Additionally, 18VAC110-20-15, relating
to criteria for delegation of informal fact-finding proceedings to an agency
subordinate, will be moved into new chapter 18VAC110-16 because it applies to
all types of licensees, registrants, and permit holders regulated by the board.
The regulatory action being considered is in response to a
periodic review of the regulations, and this Notice of Intended Regulatory
Action serves as the report of the findings of the regulatory review pursuant
to § 2.2-4007.1 of the Code of Virginia.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: §§ 54.1-2400 and 54.1-3307 of the
Code of Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Caroline Juran, RPh, Executive Director,
Board of Pharmacy, 9960 Mayland Drive, Suite 300, Richmond, VA 23233-1463,
telephone (804) 367-4416, FAX (804) 527-4472, or email
caroline.juran@dhp.virginia.gov.
VA.R. Doc. No. R16-4673; Filed June 18, 2016, 11:20 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
Regulations Governing Wholesale Distributors, Manufacturers, and Warehousers
Notice of Intended Regulatory Action
Notice is hereby given in accordance with § 2.2-4007.01 of the
Code of Virginia that the Board of Pharmacy intends to consider (i) amending 18VAC110-20,
Regulations Governing the Practice of Pharmacy, and 18VAC110-50,
Regulations Governing Wholesale Distributors, Manufacturers, and Warehousers
and (ii) adopting 18VAC110-16, Regulations Governing the Delegation of
Informal Fact-Finding Proceedings to an Agency Subordinate, and
18VAC110-25, Regulations Governing the Licensure of Pharmacists and
Registration of Pharmacy Technicians. The purpose of the proposed action is
to (i) reduce the size and complexity of 18VAC110-20 by moving some of the
provisions of that chapter into new chapters and (ii) amend 18VAC110-20 and
18VAC110-50 to clarify certain requirements, incorporate provisions currently
found in guidance documents, and update and streamline requirements where
possible. Provisions relating to the licensure of pharmacists and registration
of pharmacy technicians and certain general provisions will be moved from
18VAC110-20 to new chapter 18VAC110-25. Additionally, 18VAC110-20-15, relating
to criteria for delegation of informal fact-finding proceedings to an agency
subordinate, will be moved into new chapter 18VAC110-16 because it applies to
all types of licensees, registrants, and permit holders regulated by the board.
The regulatory action being considered is in response to a
periodic review of the regulations, and this Notice of Intended Regulatory
Action serves as the report of the findings of the regulatory review pursuant
to § 2.2-4007.1 of the Code of Virginia.
The agency intends to hold a public hearing on the proposed
action after publication in the Virginia Register.
Statutory Authority: §§ 54.1-2400 and 54.1-3307 of the
Code of Virginia.
Public Comment Deadline: August 10, 2016.
Agency Contact: Caroline Juran, RPh, Executive Director,
Board of Pharmacy, 9960 Mayland Drive, Suite 300, Richmond, VA 23233-1463,
telephone (804) 367-4416, FAX (804) 527-4472, or email
caroline.juran@dhp.virginia.gov.
VA.R. Doc. No. R16-4673; Filed June 18, 2016, 11:20 a.m.
REGULATIONS
Vol. 32 Iss. 23 - July 11, 2016
TITLE 2. AGRICULTURE
BOARD OF AGRICULTURE AND CONSUMER SERVICES
Fast-Track Regulation
Title of Regulation: 2VAC5-160. Rules and Regulations
Governing the Transportation of Horses (repealing 2VAC5-160-10 through 2VAC5-160-90).
Statutory Authority: § 3.2-6501 of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: August 10, 2016.
Effective Date: August 25, 2016.
Agency Contact: Dr. Carolynn Bissett, Program Manager,
Office of Veterinary Services, Department of Agriculture and Consumer Services,
P.O. Box 1163, Richmond, VA 23218, telephone (804) 786-2483, FAX (804)
371-2380, TTY (800) 828-1120, or email carolynn.bissett@vdacs.virginia.gov.
Basis: Section 3.2-109 of the Code of Virginia
establishes the board as a policy board with the authority to adopt regulations
in accordance with the provisions of Title 3.2 of the Code of Virginia.
Section 3.2-6501 of the Code of Virginia authorizes the board
to adopt regulations and guidelines consistent with the objectives and intent
of the Virginia Comprehensive Animal Care Law (Chapter 65 of Title 3.2 of the
Code) concerning the care and transportation of animals.
Purpose: The proposed regulatory action will repeal this
regulation that has not been utilized or applied since it was adopted over 25
years ago. The agency cannot foresee a circumstance where the regulation would
be needed in the future as there are no longer any operating horse slaughter
plants in the United States. If horse slaughter plants were to reopen in the
United States, or if Virginia horses are transported outside of the United
States for slaughter, the humane care of horses is covered under the Virginia
Comprehensive Animal Care Law. Additionally, federal regulations pertaining to
the commercial transportation of equines for slaughter can be found in 9 CFR
Part 88.
Rationale for Using Fast-Track Rulemaking Process: The
regulation has not been utilized or applied since it was adopted over 25 years
ago, and the agency cannot foresee a circumstance where the regulation would be
needed in the future as other state animal care laws and federal laws
pertaining to this topic exist. There is no longer a need for this regulation.
The agency is not aware of any stakeholders suggesting that the regulation be
retained or that the regulation is of any benefit to them.
Substance: The proposed regulatory action will repeal
this regulation that has not been utilized or applied since it was adopted over
25 years ago. The agency cannot foresee a circumstance where the regulation
would be needed in the future as there are no longer any operating horse
slaughter plants in the United States.
Issues: The primary advantage to the public is the
repeal of an outdated regulation that specifies actions that have never been
taken. The agency and the Commonwealth will no longer be in a position of
having an outdated regulation that is not enforced. This action to eliminate an
outdated, unnecessary regulation is part of good governance. There are no
disadvantages to the public or the Commonwealth associated with repealing the
regulation.
Small Business Impact Review Report of Findings:
This regulatory action serves as the report of the findings of the regulatory
review pursuant to § 2.2-4007.1 of the Code of Virginia.
Department of Planning and Budget's Economic Impact
Analysis:
Summary of the Proposed Amendments to Regulation. The Board of
Agriculture and Consumer Services (Board) proposes to repeal this regulation.
Result of Analysis. The benefits likely exceed the costs for
all proposed changes.
Estimated Economic Impact. The existing regulation provides the
rules regarding the transportation of loads of more than six horses being
transported to a commercial slaughter facility in a vehicle. The regulation
does not address the transportation of horses under other circumstances.
The regulation has not been utilized or applied since it was
adopted over 25 years ago; also, the Department of Agriculture and Consumer
Services cannot foresee a circumstance where the regulation would be needed in
the future, as there are no longer any operating horse slaughter plants in the
U.S. If horse slaughter plants were to reopen in the U.S., or if Virginia
horses are transported outside of the U.S. for slaughter, the humane care of
horses is covered under the Virginia Comprehensive Animal Care Law.1
Additionally, federal regulations pertaining to the commercial transportation
of equines for slaughter can be found in 9 CFR, Part 88.
The repeal of this regulation will have no impact beyond
potentially reducing the likelihood that readers may be misled into believing
that the transport of horses to operating horse slaughter plants is currently
done in Virginia. To the extent that the repeal of the regulation reduces the
likelihood of such confusion, the proposed repeal would be beneficial.
Businesses and Entities Affected. Since there are no operating
horse slaughter plants in the U.S. and this regulation has not been utilized or
applied since it was adopted over 25 years ago, its repeal will not
significantly affect any businesses or entities.
Localities Particularly Affected. The proposed repeal of the
regulation does not disproportionately affect particular localities.
Projected Impact on Employment. The proposed repeal of the
regulation does not affect employment.
Effects on the Use and Value of Private Property. The proposed
repeal of the regulation does not affect the use and value of private property.
Real Estate Development Costs. The proposed repeal of the
regulation does not affect real estate development costs.
Small Businesses:
Definition. Pursuant to § 2.2-4007.04 of the Code of Virginia,
small business is defined as "a business entity, including its affiliates,
that (i) is independently owned and operated and (ii) employs fewer than 500
full-time employees or has gross annual sales of less than $6 million."
Costs and Other Effects. The proposed repeal of the regulation
does not affect small businesses.
Alternative Method that Minimizes Adverse Impact. The proposed
repeal of the regulation does not affect small businesses.
Adverse Impacts:
Businesses. The proposed repeal of the regulation will not
adversely affect businesses.
Localities. The proposed repeal of the regulation will not
adversely affect localities.
Other Entities. The proposed repeal of the regulation will not
adversely affect other entities.
_________________
Agency's Response to Economic Impact Analysis: The
agency concurs with the analysis of the Department of Planning and Budget.
Summary:
The regulatory action repeals the chapter, which has not
been utilized or applied since it was adopted over 25 years ago. The
agency cannot foresee a circumstance where the regulation would be needed in
the future as other state animal care laws and federal laws pertaining to this
topic exist. Therefore, the regulation is repealed.
VA.R. Doc. No. R16-4645; Filed June 21, 2016, 11:27 a.m.
TITLE 2. AGRICULTURE
BOARD OF AGRICULTURE AND CONSUMER SERVICES
Fast-Track Regulation
Title of Regulation: 2VAC5-501. Regulations Governing
the Cooling, Storing, Sampling and Transporting of Milk (amending 2VAC5-501-10, 2VAC5-501-50 through 2VAC5-501-90;
repealing 2VAC5-501-110).
Statutory Authority: §§ 3.2-5206, 3.2-5223, and 3.2-5224
of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: August 10, 2016.
Effective Date: August 25, 2016.
Agency Contact: Robert Trimmer, Program Supervisor,
Department of Agriculture and Consumer Services, P.O. Box 1163, Richmond, VA
23218, telephone (804) 786-1452, FAX (804) 371-7792, TTY (800) 828-1120, or
email robert.trimmer@vdacs.virginia.gov.
Basis: Section 3.2-109 of the Code of Virginia
establishes the Board of Agriculture and Consumer Services as a policy board
and authorizes the board to adopt regulations in accordance with the provisions
of Title 3.2 of the Code of Virginia.
Section 3.2-5206 of the Code of Virginia authorizes the board
to establish definitions and standards of quality and identity and to adopt and
enforce regulations dealing with the issuance of permits, production,
importation, processing, grading, labeling, and sanitary standards for milk,
milk products, market milk, market milk products, and those products
manufactured or sold in semblance to or as substitutes for milk, milk products,
market milk, or market milk products.
This section also authorizes the board to adopt (i) any
regulation or part thereof under federal law that pertains to milk or milk
products, amending the federal regulation as necessary for intrastate
application and (ii) any model ordinance or regulation issued under federal law
including the Pasteurized Milk Ordinance (PMO) and the U.S. Department of
Agriculture's Milk for Manufacturing Purposes.
Purpose: The amendments bring the regulation in line
with current federal standards as established by the 2013 revision of the PMO.
In addition to providing for consistency with current federal standards and
existing Virginia regulations, these amendments provide for sufficient
flexibility regarding milk storage times for the dairy industry while
continuing to protect the public's health, safety, and welfare by ensuring the
safety and wholesomeness of all milk shipped from Virginia dairy farms.
Surrounding states have already updated their regulations to be
consistent with the less stringent requirements established in the revised PMO
governing the storage and transportation of milk. The changes facilitate
interstate sales of Virginia milk producers by providing a level playing field
with surrounding states in regards to the storage and transportation of milk.
The regulatory modifications should effect a cost savings to producers associated
with the transportation of milk from farms to processing facilities with no
adverse effects on the health and safety of consumers.
Rationale for Using Fast-Track Rulemaking Process: The
amendments are noncontroversial changes requested by the dairy industry and
bring the regulation in line with current federal standards and regulations
adopted by surrounding states. The amendments are less stringent than the
requirements currently in place, and producers are not required to exercise the
72-hour storage option. The additional 20 hours of storage provided for in the
amendments does not affect the safety of the milk supply and reduces producer
costs associated with the transportation of milk. The amendment aids producers
during extreme weather events that disrupt normal transportation by increasing
the permissible storage time and reducing the need to seek emergency variances
during such weather events.
Substance: The substantive changes are as follows:
1. The addition of 20 hours of milk storage time in a farm bulk
tank, allowing for the sale of milk no older than 72 hours from completion of
the first milking. The current regulation allows 52 hours of storage time in a
farm bulk tank.
2. Allows for a 24, 48, or 168 hour (seven day) rotation of
recording charts based on the frequency of milk pick up. These changes align
the regulations with existing federal regulation and regulations of surrounding
states.
The removal of 2VAC5-501-110 from the chapter since this
section is no longer relevant and is unnecessary for the enforcement of
2VAC5-501.
Issues: The primary advantage to the public is that the
regulation allows for the safe storage and cooling of milk produced on dairy
farms in Virginia and sold in intrastate and interstate commerce. This ensures
that the public is afforded the opportunity to consume a safe product and
further ensures that the dairy industry is afforded additional flexibility
regarding the storage of milk.
The primary advantage to the agency and Commonwealth is that
the regulation ensures that the Commonwealth can adequately protect the public.
The requirements also aid the continued intrastate and interstate sale of milk
on a more competitive basis, which ultimately benefits Virginia's economy.
This regulatory action poses no disadvantages to the public or
the Commonwealth.
Small Business Impact Review Report of Findings: This
regulatory action serves as the report of the findings of the regulatory review
pursuant to § 2.2-4007.1 of the Code of Virginia.
Department of Planning and Budget's Economic Impact
Analysis:
Summary of the Proposed Amendments to Regulation. The
Department of Agriculture and Consumer Services (DACS) proposes to increase the
permissible storage time of milk in a farm bulk tank from 52 hours to 72 hours
and to allow the use of chart recorders supporting a 72-hour pick up schedule.
Result of Analysis. The benefits likely exceed the costs for
all proposed changes.
Estimated Economic Impact. In most farms once milk is obtained
from the cow it is stored in a tank to be picked up by a hauler at certain
frequencies to be delivered to the processing plant. Under the current
regulations, producers can store milk in a farm tank up to 52 hours. However,
the permissible storage time in surrounding states as well as the standard established
in the federal Pasteurized Milk Ordinance is 72 hours. The proposed regulation
will allow storage of milk in Virginia farms up to 72 hours.
An increase in storage time would allow producers to reduce the
frequency of pick-ups from the farm; albeit lower frequency pick-ups may
require a larger tank and a new chart recorder. According to DACS, haulers
usually charge $65 to $100 per pick-up; the cost of a storage tank is about
$100 per gallon of capacity; and a recorder that can support a 72-hour rotation
schedule costs about $1,800. The proposed regulation allows but does not
require storage of milk up to 72 hours. Thus, producers that anticipate savings
from less frequent pick-ups will be allowed to do so under the proposed
regulation. The proposed change may also reduce the need to seek emergency
variances during extreme weather events. Given the federal ordinance and the
permissible storage times from neighboring states, the proposed increase in the
storage time is not expected to affect the safety of milk supply or pose any
health risks.
In addition, consistency with dairy industry standards in
surrounding states would promote competition. Virginia farmers will now be able
to reduce their transportation costs to the levels comparable to those of
producers in other states which may promote production. Since Virginia's
current storage times are more restrictive than the other states, there may
also be an increase in the quantity of milk imported to the Commonwealth
further promoting competition.
The remaining proposed changes are clarifying in nature and are
not expected to create any significant economic effects other than improving
the clarity of the regulation.
Businesses and Entities Affected. There are 639 estimated Grade
"A" milk producers in Virginia. Some of these producers may already
have the storage tank capacity and a chart recorder to accommodate a 72-hour
pick-up schedule. There are 281 licensed haulers that drive the trucks and pick
up milk and 17 companies in and out of state that hire them. There are
approximately five dairy equipment dealers in Virginia that represent or
distribute for a number of dairy equipment manufacturers.1
Localities Particularly Affected. The proposed changes apply
statewide.
Projected Impact on Employment. The proposed changes will allow
the dairy industry to reduce transportation costs and improve competition. An
increase in competition may lead to more production and an increased demand for
labor. In addition, demand for storage tanks and chart recorders may increase.
On the other hand, less frequent milk pick up times has the potential to reduce
the demand for transportation services offered by milk haulers.
Effects on the Use and Value of Private Property. The proposed
changes may have a positive impact on asset values of some producers of milk,
manufacturers, distributors, and installers of storage tanks and chart
recorders, and may have a negative impact on asset values of some milk haulers
and businesses that hire them.
Real Estate Development Costs. No impact on real estate
development costs is expected.
Small Businesses:
Definition. Pursuant to § 2.2-4007.04 of the Code of Virginia,
small business is defined as "a business entity, including its affiliates,
that (i) is independently owned and operated and (ii) employs fewer than 500
full-time employees or has gross annual sales of less than $6 million."
Costs and Other Effects. Most of the producers of milk, milk
haulers, distributors and installers of tanks and recorders are considered
small businesses. The potential effects on them are the same as those discussed
above.
Alternative Method that Minimizes Adverse Impact. There is no
known alternative to minimize the potential adverse impact on milk haulers and
businesses that hire them while achieving the intended policy goals.
Adverse Impacts:
Businesses. The proposed amendments are not anticipated to have
an adverse impact on non-small businesses.
Localities. The proposed amendments will not adversely affect
localities.
Other Entities. The proposed amendments will not adversely
affect other entities.
_______________________
1 Data source: Department of Agriculture and Consumer
Services
Agency's Response to Economic Impact Analysis: The
agency concurs with the analysis of the Department of Planning and Budget.
Summary:
The amendments (i) add 20 hours of milk storage time in a
farm bulk tank, allowing for the sale of milk no older than 72 hours from
completion of the first milking; (ii) allow the use of a 24-hour, 48-hour, or
168-hour (seven-day) chart recorder based upon the frequency of milk pickup
from producers; and (iii) update certain standards incorporated by reference.
2VAC5-501-110 is repealed as it is no longer necessary for the enforcement of
the chapter.
2VAC5-501-10. Definitions.
The following words and terms when used in this chapter shall
have the following meanings unless the context clearly indicates otherwise:
"Bulk milk hauler" means any person who holds a
permit issued by the Virginia Department of Agriculture and Consumer Services
to collect official milk samples and transport: (i) raw milk from a
dairy farm to a milk plant, receiving station, or transfer station; or (ii) raw
milk products from one milk plant, receiving station, or transfer station to
another milk plant, receiving station, or transfer station.
"Bulk milk pickup tanker" means a vehicle,
including the truck, tank, and those appurtenances necessary for its use, used
by a bulk milk hauler or bulk milk sampler to transport bulk raw milk for
pasteurization from a dairy farm to a milk plant, receiving station, or
transfer station.
"Bulk milk pickup tanker commingled milk" means the
commingled raw milk from two or more dairy farms which that has
not been removed from the bulk milk pickup tanker.
"Bulk milk sampler" means any person who holds a
permit issued by the Virginia Department of Agriculture and Consumer Services
to collect, store, or transport official milk samples.
"Cancel" means to permanently nullify, void, or
delete a permit issued by the Virginia Department of Agriculture and Consumer
Services.
"Contract hauler" or "subcontract hauler"
means any person who contracts; (i) to transport raw milk from a dairy
farm to a milk plant, receiving station, or transfer station; or (ii) to
transport raw milk or milk products between a milk plant, receiving station, or
transfer station and another milk plant, receiving station, or transfer
station.
"Dairy farm" means any place or premises (i)
where any cow, goat, sheep, water buffalo, or other mammal (except humans) is
kept, or (ii) from which any cow, goat, sheep, water buffalo, or
other mammal (except humans) milk, dairy product, or milk product is sold or
offered for sale for human consumption.
"Dairy plant sampler" means any employee of:
(i) a milk plant who is responsible for collecting official milk samples in the
Commonwealth of Virginia;, (ii) the Virginia Department of
Agriculture and Consumer Services who is responsible for collecting raw milk or
pasteurized milk product samples at a milk plant;, or (iii) the
Virginia Department of Health who is responsible for collecting raw milk or
pasteurized milk product samples at a milk plant and who holds a permit issued
by the Virginia Department of Agriculture and Consumer Services for the collection
of official milk samples for regulatory purposes.
"Dairy product" means butter, natural or processed
cheese, dry whole milk, nonfat dry milk, dry buttermilk, dry whey, evaporated
whole or skim milk, condensed whole milk, and condensed plain or sweetened skim
milk.
"Deny" means the Virginia Department of Agriculture
and Consumer Services will not issue a permit to the applicant.
"Farm bulk cooling or holding tank" means any tank
installed on a dairy farm for the purpose of cooling or storing raw milk.
"Milk" means the whole, fresh, clean lacteal
secretion obtained by the complete milking of one or more healthy cows, goats,
sheep, water buffalo, or other mammal (except humans) intended for human
consumption excluding that obtained before and after birthing for such a period
as may be necessary to render the milk practically colostrum-free.
"Milk plant" means any place, premises, or
establishment where milk, milk products, or dairy products are collected,
handled, processed, stored, pasteurized, aseptically processed, bottled,
packaged, or prepared for distribution.
"Milk producer" means any person who operates a
dairy farm and provides, sells, or offers any milk for human consumption.
"Milk product" means: (i) acidified lowfat
milk, acidified milk, acidified milk product, acidified skim milk, acidified
sour cream, acidified sour half-and-half, aseptically processed milk,
aseptically processed milk product, buttermilk, coffee cream, concentrated
milk, concentrated milk product, cottage cheese, cottage cheese dry curd,
cream, cultured half-and-half, cultured milk, cultured lowfat milk, cultured
skim milk, cultured sour cream, dry curd cottage cheese, eggnog,
eggnog-flavored milk, flavored milk, flavored milk product, fortified milk,
fortified milk product, frozen milk concentrate, goat milk, half-and-half,
heavy cream, lactose-reduced lowfat milk, lactose-reduced milk, lactose-reduced
skim milk, light cream, light whipping cream, lowfat cottage cheese, lowfat
milk, lowfat yogurt, low-sodium lowfat milk, low-sodium milk, low-sodium skim
milk, milk, nonfat milk, nonfat yogurt, recombined milk, recombined milk
product, reconstituted milk, reconstituted milk product, sheep milk, skim milk,
sour cream, sour half-and-half, table cream, vitamin D milk, vitamin D milk
product, whipped cream, whipped light cream, whipping cream, or yogurt; (ii)
any of the following foods: milk, lowfat milk, or skim milk with added safe and
suitable microbial organisms; or (iii) any food made with a food specified in clause
(i) of this definition by the addition or subtraction of milkfat or addition of
safe and suitable optional ingredients for protein, vitamin, or mineral
fortification. Milk products also include those dairy foods made by modifying
the federally standardized products listed above in this definition
in accordance with 21 CFR 130.10 - Requirements for foods named by use of a
nutrient content claim and a standardized term.
"Milk tank truck" means the term used to describe
both a bulk milk pickup tanker and a milk transport tank.
"Milk tank truck cleaning facility" means any
place, premise, or establishment, separate from a milk plant, receiving
station, or transfer station where a bulk milk pickup tanker or milk transport
tank is cleaned and sanitized.
"Milk transport tank" means a vehicle, including
the truck and tank, used by a bulk milk hauler to transport bulk shipments of
milk, milk product, or dairy product from a milk plant, receiving station, or
transfer station to another milk plant, receiving station, or transfer station.
"Official laboratory" means a facility where
biological, chemical, or physical testing is performed that is operated or
approved by the state regulatory authority.
"Official milk sample" means each sample of milk,
milk product, or dairy product that is collected for compliance with
requirements of this chapter by a person who holds a permit to collect milk,
milk product, or dairy product samples issued by the state regulatory
authority.
"Other mammals" means any mammal except humans,
cows, goats, sheep, or water buffalo.
"Pay purpose laboratory" means a laboratory that
conducts tests for the purpose of determining the composition of milk, milk
product, cream, or dairy product as a basis for payment in buying or selling
any milk, milk product, cream, or dairy product.
"Permit" means the written document issued by the
Virginia Department of Agriculture and Consumer Services to a person qualified
to (i) be a bulk milk hauler, bulk milk sampler, contract hauler,
subcontract hauler, dairy plant sampler, or pay purpose tester,
or to (ii) operate a pay purpose laboratory, bulk milk pickup
tanker, or milk transport tank.
"Person" means any individual, plant operator,
partnership, corporation, company, firm, trustee, institution, or association.
"Raw" means unpasteurized.
"Receiving station" means any place, premises, or
establishment where any milk, milk product, or dairy product is received,
collected, handled, stored or cooled, and prepared for further transporting.
"Revoke" means to permanently annul, repeal,
rescind, countermand, or abrogate the opportunity for any person or persons to
hold a permit issued by the Virginia Department of Agriculture and Consumer
Services.
"State regulatory authority" means the Virginia
Department of Agriculture and Consumer Services, the agency having jurisdiction
and control over the matters embraced within this chapter.
"Summarily suspend" means the immediate suspension
of a permit issued by the state regulatory authority without the permit holder
being granted the opportunity to contest the action prior to the effective date
and time of the suspension.
"Suspend" means to temporarily nullify, void,
debar, or cease for a period of time a permit issued by the Virginia Department
of Agriculture and Consumer Services.
"Transfer station" means any place, premises, or
establishment where milk, dairy products, or milk products are transferred
directly from one milk transport milk tank to another, or from
one or more bulk milk pickup tankers to one or more milk transport milk
tanks.
"Transport-commingled milk" means any raw milk,
milk product, or dairy product that has been removed from one or more bulk milk
pickup tankers or any silo, vat, or container in a milk plant and loaded into a
milk transport tank.
"Transport tank operator" means any person who
hauls transport-commingled milk.
"3-A Sanitary Standards" means the standards for
dairy equipment and accepted practices formulated by the 3-A Sanitary Standards
Committees representing the International Association for Food Protection, the U.
S. U.S. Public Health Service, and the Dairy Industry Committee and
published by the International Association for Food Protection.
2VAC5-501-50. Cooling temperature and storage standards for
milk stored on a dairy farm.
A. Each person who that operates a dairy farm
shall cool his raw milk to 40°F or cooler, but not frozen, within two
hours after milking and the temperature at any time thereafter shall not be
warmer than 50°F. Raw milk that is warmer than a temperature of 50°F two hours
after the first milking or at any time thereafter shall be deemed a public
health hazard and shall not be utilized in any milk, milk product, or dairy
product, offered for sale, or sold.
B. No person who that operates a dairy farm and
holds a grade "A" dairy farm permit shall sell or offer to sell any
milk as grade "A" milk if the age of the milk is older than 52
72 hours after the completion of the first milking.
C. No person who that operates a dairy farm and
holds a permit to produce milk for manufacturing purposes shall sell, offer to
sell, or process any milk for manufacturing purposes if the age of the milk is
older than 76 hours after the completion of the first milking. Raw milk for
manufacturing purposes older than 76 hours shall be deemed to be a public
health hazard.
2VAC5-501-60. Construction and operation of farm bulk milk
cooling or holding tanks, recording thermometers, interval timing devices, and
other required milkhouse or milkroom facilities.
A. Each person who that operates a dairy farm
and installs one or more farm bulk cooling or holding tanks in his the
milkhouse shall provide the following facilities:
1. A milk hose port opening no larger than eight inches in
diameter through a wall in the milkhouse closest to the area the bulk milk
pickup tanker will be parked to receive the milk from each farm bulk cooling or
holding tank;. The hose port shall be:
a. Provided with a self-closing door that shall open to the
outside; and
b. Of sufficient height above the milkhouse floor and the
outside apron to prevent flooding or draining of the milkhouse;
2. The hose port shall be provided with a self-closing door
which shall open to the outside;
3. The hose port shall be of sufficient height above the
milkhouse floor and the outside apron to prevent flooding or draining of the
milkhouse;
4. 2. An outside apron constructed of concrete
or other equally impervious material shall be provided on the outside of the
milkhouse directly beneath the hose port to protect the milk-conducting
equipment from contamination;, and:
a. If constructed of concrete, each outside apron shall be
a minimum of four inches thick and measure a minimum of two feet by two feet
horizontally; or
b. If constructed of a material other than concrete, each
outside apron shall measure a minimum of two feet by two feet horizontally;
5. Each outside apron shall be a minimum of four inches
thick if constructed of concrete and measure a minimum of two feet by two feet
horizontally;
6. Each outside apron constructed of a material other than
concrete shall measure a minimum of two feet by two feet horizontally;
7. 3. A 220-volt grounded weatherproof
electrical outlet installed on the outside of the milkroom or milkhouse near
the hoseport for the bulk milk hauler's use to power the milk pump on the bulk
milk pickup tanker; and
8. 4. A switch to control the electrical power
to the 220-volt grounded weatherproof electrical outlet located on the inside
of the milkroom or milkhouse near the outlet to the farm bulk cooling or
holding tank.
B. Each person who that operates a dairy farm
and installs one or more farm bulk cooling or holding tanks in his the
milkhouse or milkroom shall comply with the following requirements:
1. Each farm bulk cooling or holding tank shall comply with
all the requirements contained in:
a. 3-A Sanitary Standards for Farm Milk Cooling and Holding
Tanks, Document No. 13-09 (Nov. 1993) 13-11 (July 2012); or
b. 3-A Sanitary Standards for Farm Milk Storage Tanks,
Document No. 30-01 (Sept. 1984);
2. Each farm bulk cooling or holding tank shall be equipped
with an indicating thermometer accurate to plus or minus 2.0°F and capable of
registering the temperature of the milk in the tank before it reaches 10% of
the tank's volume;
3. Each farm bulk cooling or holding tank shall be installed
to comply with the following minimum clearance distances around, above, and
below each farm bulk cooling or holding tank:
a. Three feet measured horizontally between a wash vat and the
outermost portion of any farm bulk cooling or holding tank;
b. Three feet measured horizontally in a 180-degree arch from
the front of the tank where the outlet valve is located;
c. Two feet measured horizontally from the sides and rear of
any farm bulk cooling or holding tank to any wall, shelves, water heater,
hand-basin, or other object;
d. Eighteen inches measured horizontally from the outermost
portion of any farm bulk cooling or holding tank to any floor drain and the
floor drain shall not be located underneath the tank;
e. Three feet measured vertically from the top of the manhole
cover of any farm bulk cooling or holding tank to the ceiling;
f. Eight inches measured vertically from the floor underneath
the bottom of any round farm bulk cooling or holding tank that measures greater
than 72 inches in diameter;
g. Four inches measured vertically from the floor underneath
the bottom of any round farm bulk cooling or holding tank that measures equal
to or less than 72 inches in diameter; and
h. Six inches measured vertically from the floor underneath
the bottom of any flat bottom farm bulk cooling or holding tank;
4. Farm bulk cooling or holding tanks installed through a
milkroom wall shall meet the following minimum requirements:
a. The area between the farm bulk cooling or holding tank and
the wall shall be tightly sealed;
b. All vents and openings on the farm bulk cooling or holding
tank located outside the milkroom shall be protected from dust, insects,
moisture, and other debris which might enter the tank; and
c. All agitators located outside the milkroom shall be
equipped with a tightly fitting seal between the bottom of the agitator motor
and the top of the farm bulk cooling or holding tank;
5. Each person who that operates a dairy farm
shall ensure that each farm bulk cooling or holding tank is installed with a
foundation of sufficient strength to support the tank when it is full;
6. Each person who that operates a dairy farm shall
obtain prior approval from the state regulatory authority for each farm bulk
cooling or holding tank and its installation before it is installed on the
person's dairy farm; and
7. Each person who that operates a dairy farm
shall ensure each farm bulk cooling or holding tank on his the
farm is installed, gauged, and a volume chart prepared in compliance with § 3.2-5260
regulations adopted pursuant to § 3.2-5206 of the Code of Virginia.
Each farm bulk cooling or holding tank and any gauge rod, surface gauge, gauge,
or gauge tube and calibration chart associated with it shall be identified by
serial number in a prominent manner.
C. Each person who that holds a grade
"A" dairy farm permit and installs a farm bulk cooling or holding
tank shall comply with the following:
1. Each farm bulk cooling or holding tank shall be equipped
with a recording thermometer;
2. Each recording thermometer shall be installed to comply
with the following:
a. Each recording thermometer shall be installed in the
milkhouse;
b. No recording thermometer may be installed on or attached to
a farm bulk cooling or holding tank;
c. Each recording thermometer shall be installed: (i)
on an inside wall of the milkhouse;, (ii) on an outside wall of
the milkhouse or milkroom if installed with one inch of rigid insulation
between the back of the recording thermometer and the surface of the outside
wall;, or (iii) on metal brackets from the ceiling or floor; and
d. Each recording thermometer sensor shall be installed on the
farm bulk cooling or holding tank to record the temperature of the milk in the
tank before the milk reaches 10% of the tank's volume;
3. Standards for recording thermometers. Each recording
thermometer installed on a farm bulk cooling or holding tank shall comply with
the following minimum requirements:
a. The case for each recording thermometer shall be moisture
proof under milkhouse conditions;
b. The case for each recording thermometer shall be UL rated
NEMA 4X enclosure or equivalent as provided in ANSI/NEMA 250, Enclosures for
Electrical Equipment (1000 Volts Maximum) dated August 30, 2001 December
29, 2014;
c. The case for each recording thermometer shall be equipped
with a corrosion-resistant latching mechanism that keeps the recording
thermometer tightly closed;
d. The recorder chart for each recording thermometer shall not
exceed a maximum chart rotation time of 48 168 hours (seven
days). Recorder charts for farm bulk cooling or holding tanks that are
picked up every other day shall have a chart rotation time of 48 hours.
Recorder charts for farm bulk cooling or holding tanks that are picked up every
day may have a chart rotation time of 24 or 48 hours;
e. The recorder chart for each recording thermometer shall be
marked with water resistant ink;
f. The scale on the recording chart shall cover a minimum of
30°F to 180°F, with the scale reversed to show cold temperatures at the outside
of the chart for best resolution;
g. Each division on the recording chart shall represent a
maximum of 1.0°F between 30°F and 60°F, with two degree divisions between 60°F
and 180°F;
h. Spacing of divisions on the recorder chart shall be a
minimum of 0.040 inches per 2.0°F, with the ink line easily distinguishable
from the printed line;
i. The recording thermometer speed of response or sensing of
temperature shall be a maximum of 20 seconds;
j. The recording thermometer shall be accurate to plus or
minus 2.0°F;
k. The sensor for each recording thermometer shall be:
(i) a resistance temperature detector (RTD) type sensor;, (ii)
constructed of stainless steel type 304 or type 316 on all exterior surfaces;,
(iii) hermetically sealed;, (iv) accurate to 0.3°C;,
and (v) continuous run wire;
l. Each recording thermometer and sensor shall be calibrated
and supplied as a package;
m. No capillary system containing any toxic gas or liquid
shall be allowed to come into direct contact with any milk or milk product;
n. Other recording devices may be accepted by the state
regulatory authority if they comply with the requirements of subdivisions 3 a
through m of this subsection;
o. If a strip chart style recorder is used, it shall move not
less than one inch per hour, and may be continuous for a maximum of 30
days; and
p. Recording thermometers may be manually wound or
electrically operated;
4. Recording thermometer operation: Each recording
thermometer installed on a farm bulk cooling or holding tank shall comply with
the following minimum operating requirements:
a. Each recording thermometer shall be provided with a means
to seal the calibration and zeroing mechanism to provide evidence of
unauthorized adjustment or tampering;
b. Each recording thermometer shall be provided with a pin in
the hub to prevent the recording chart from being rotated; and
c. Each recording thermometer shall be properly grounded and
short circuit protected;
5. Each person who that operates a dairy farm
and installs a recording thermometer on his the farm bulk cooling
or holding tank shall maintain a minimum of a 30-day supply of unused recorder
charts designed for the specific recording thermometer he installed and shall
maintain a minimum of the past 60 days of used charts for purposes of
inspection; and
6. Each person who that operates a dairy farm
and installs a recording thermometer on his the farm bulk cooling
or holding tank shall provide a moisture proof storage container in the
milkhouse or milkroom for purpose of storing a supply of new charts and a
minimum of 60 days of used charts;.
D. No person may remove from the dairy farm any recorder
chart that has been used once and removed from the recorder within the past 60
days unless he has obtained permission from the state regulatory authority. All
recorder charts removed from any dairy farm by any person other than a
representative of the state regulatory authority shall be returned to the dairy
farm within ten 10 days. All recorder charts shall be available
to the state regulatory authority.
E. Handling of recording charts. Each bulk milk hauler
shall comply with the following requirements when picking up milk from a dairy
farm if the farm bulk cooling or holding tank is equipped with a recording
thermometer:
1. Each milk hauler, in making a milk pickup, shall properly
agitate the milk and remove the chart from the recorder;
2. Each milk hauler shall record the following information on
each chart removed from the recorder:
a. The date and time of pickup; and
b. The signature of the milk hauler;
3. Each milk hauler shall store the used chart in the storage
container supplied by the dairy farmer;
4. Each milk hauler shall obtain a new chart from the supply
provided by the dairy farmer and record the following information in the chart:
a. The date; and
b. The patron number of the dairy farmer;
5. If a recorder chart is used for more than one pickup, each
milk hauler shall identify each lot of milk on the chart with the date, time of
pickup, and his signature; and
6. Before removing any milk from the farm tank, each milk
hauler shall check the recorder chart. If the recorder chart indicates that the
milk temperature has varied in a manner that would preclude acceptance, he
shall immediately notify his superior and the dairy farmer. If the milk is
rejected, each milk hauler shall record this information on the chart. If the
milk is picked up, each milk hauler shall sign the chart and record the date
and time of pickup;.
F. Maintenance of recording thermometers. Each person who
that operates a dairy farm and holds a grade "A" dairy farm
permit shall be responsible for maintaining each of his the
recording thermometers in good repair and adjustment to include calibrating the
recording thermometer to read accurately within plus or minus 2.0°F of the
actual milk temperature in the farm bulk cooling or holding tank.
G. Sealing of recording thermometers: Each recording
thermometer installed on a farm bulk cooling or holding tank shall be inspected
and may be sealed by the state regulatory authority after it has been shown to
be properly installed and calibrated.
H. Each person who that holds a grade
"A" dairy farm permit and installs a farm bulk cooling or holding
tank shall:
1. Install on each farm bulk cooling or holding tank an
interval timing device that automatically agitates the milk in the farm bulk
tank for not less than five minutes every hour during the entire time milk is
being cooled or stored in the tank;
2. Not install a manual switch capable of turning off the
interval timing device on any farm bulk milk cooling or holding tank while any
milk is being cooled or stored; and
3. Maintain in good repair and operating condition each
interval timing device installed on his the farm bulk cooling or
holding tank.
2VAC5-501-70. Measuring, sampling, and testing.
A. Quantity measurements. Each person who determines
the quantity of milk in any lot of milk being picked up on any dairy farm in
Virginia shall comply with one of the following:
1. If the milk is being picked up from a farm bulk cooling or
holding tank, the person shall use only a measuring rod, gauge, or gauge tube
accurately calibrated to the individual farm bulk cooling or holding tank and
the accompanying calibration chart with a serial number that matches the serial
number for the specific farm bulk cooling or holding tank for which it was
prepared;
2. If the milk being picked up is not stored in a farm bulk
cooling or holding tank, the person shall determine the quantity of milk at the
point of delivery to the milk plant processing the milk by commingling all of
the milk in a vessel equipped with a gauge rod, surface gauge, gauge, or gauge
tube and a volume chart that has been prepared in compliance with § 3.2-5620
of the Code of Virginia;
3. If the milk being picked up is not stored in a farm bulk
cooling or holding tank and the basis for payment for the milk will be based
solely on the volume of milk in gallons, the person shall determine the
quantity of milk by adding the volume in gallons of each separate full
container and the volume in gallons of any milk in containers that are not
full; or
4. If the milk being picked up is not stored in a farm bulk
cooling or holding tank and the basis for payment for the milk will be based
solely on the pounds of milk delivered, the person shall determine the quantity
of milk in pounds by weighing each of the containers of milk on a commercial
scale before and after they have been emptied and subtracting the weight of the
empty containers from the total weight of the containers and the milk, the
difference being the weight in pounds of milk.
B. Each person who desires to convert a volumetric
measurement of milk to weight in pounds of milk shall multiply the volume of milk
in gallons by 8.60.
C. Each person who that operates a dairy farm
and transports any milk in cans or other containers from his the
dairy farm to a milk plant and intends to determine the basis for payment of his
the milk based solely on its volume in gallons or solely on its weight
in pounds, shall ensure the cans or other containers comply with the following:
1. Each container shall be provided with a visual means to
measure the volume of milk in the container in divisions of one or more whole
gallons up to the total capacity of the container;
2. Each container shall be equipped with a tightly fitting lid
that prevents any milk from leaking out around the closure;
3. Each container shall be manufactured from stainless steel,
food grade plastic, or tinned metal;
4. No container shall be manufactured from glass or other
easily breakable material;
5. Each container shall be smooth and easily cleanable; and
6. Each container shall be equipped with an opening large
enough to allow the container to be washed by hand if it is intended to be
washed by hand or washed by mechanical means if it is intended to be washed by
mechanical means.
D. Each person who that operates a pay purpose
laboratory shall:
1. Provide a separate room of sufficient size in which pay
purpose testing shall be conducted;
2. Provide lighting of at least 20 foot-candles when measured
at work bench levels and at all other work areas used to conduct testing;
3. Provide adequate ventilation sufficient to prevent
condensation from forming and to prevent noxious or hazardous chemical fumes
from collecting in the laboratory;
4. Provide heating and cooling equipment sufficient to
maintain a constant room temperature of 70°F plus or minus 2.0°F in his
laboratory at all times;
5. Provide a separate permanently installed hand-washing
facility with hot and cold running water under pressure supplied through a mix
valve, soap, and single service paper towels;
6. Provide only potable water under pressure in his the
laboratory;
7. Provide walls that are constructed of impervious material
with a light-colored material and that are easily cleanable;
8. Provide floors made of concrete or other equally impervious
material that are easily cleanable;
9. Provide toilet facilities for his employees;
10. Use only methods and equipment approved by the state
regulatory authority to test milk for protein, solids, solids not fat, and fat;
11. Construct the facility to insure ensure that
the laboratory environment has a stable electrical supply, stable water
supply, stable heating and cooling, and stable ventilation to allow a
constantly controllable environment for pay purpose testing procedures and pay
purpose equipment; and
12. Dispose of all liquid, solid, and gaseous wastes in a
manner that complies with state and federal requirements for waste disposal.
E. Sampling. Each bulk milk hauler shall:
1. Collect at least two representative samples from each bulk
milk cooling or holding tank each time that milk is picked up from the dairy farm
for use as official milk samples;
2. Collect a minimum of four ounces of milk for each official
milk sample collected;
3. Maintain custody of all official milk samples collected or
transfer custody of all official milk samples collected to another permitted
bulk milk hauler, bulk milk sampler, or at the discretion of the state
regulatory agency, lock all official milk samples in a suitable container in
which they may be transported or stored;
4. Pickup Pick up all of the milk in each farm
bulk cooling or holding tank each time that milk is picked up from the farm
bulk cooling or holding tank; and
5. Pick up only milk that is 45°F or cooler, but not frozen.
F. Butterfat testing. Each person who desires to
determine the butterfat content of milk as a basis for payment shall: 1.
Select either select from each dairy farm supplying them with milk a
minimum of four milk samples taken at irregular intervals each month and
utilize only laboratory butterfat test results from milk samples that have been
tested within 48 hours of collection for pay purposes; or:
2. 1. Collect a representative sample from each
shipment of each producer supplying them with milk for a maximum of 16 days, if
composite milk samples are used to determine butterfat content;
3. 2. Store composite milk samples only in an
approved milk laboratory that will perform the butterfat test;
4. 3. Preserve all composite milk samples with
an appropriate preservative designed to prevent the spoilage of milk and that
will not affect the butterfat test; and
5. 4. Test each composite milk sample within
three days following the end of the number of days used to create the composite
milk sample.
2VAC5-501-80. Farm bulk milk pickup tanker and milk transport
tank requirements.
A. Each contract hauler or subcontract hauler shall:
1. Use only a farm bulk milk pickup tanker or a milk transport
tank that complies with all the requirements contained in 3-A Sanitary
Standards for Stainless Steel Automotive Transportation Tanks for Bulk Delivery
and Farm Pick-Up Service, Number 05-15 (effective November 24, 2002), (3-A
Sanitary Standards, Incorporated) and that are maintained in good repair;
2. Ensure that all appurtenances of each farm bulk milk pickup
tanker or each milk transport tank including any hoses, pumps, and fittings
comply with all applicable the requirements contained in 3-A
Sanitary Standards for Stainless Steel Automotive Transportation Tanks for
Bulk Delivery and Farm Pick-Up Service, Number 05-15 (effective as of
November 20, 2001) 24, 2002), (3-A Sanitary Standards,
Incorporated) for construction and are maintained in good repair;
3. Provide sample racks for holding all milk samples collected
in the sample cooler;
4. Provide a sample dipper or other sampling device of
sanitary design that is maintained clean and in good repair;
5. Provide milk sample storage coolers that have sufficient
insulation to maintain proper milk temperatures under all conditions throughout
the year;
6. Provide only sterile sample bags, tubes, or bottles,
properly stored to prevent contamination;
7. Provide a calibrated pocket thermometer certified as
accurate within plus or minus 2.0°F to each bulk milk hauler in his employ and
ensure the pocket thermometer is recertified a minimum of each six months
thereafter;
8. Provide a United States U.S. Environmental
Protection Agency approved and registered sanitizer for the sample dipper
container;
9. Provide a suitable sanitizer test kit to each bulk milk
hauler in his employ for use in checking the strength of sanitizing solutions;
10. Ensure that each appurtenance requiring flexibility for
the milk transfer system to operate properly is free draining, supported to
maintain a uniform slope and alignment, and easily disassembled and accessible
for inspection without the use of tools;
11. Ensure that each farm bulk milk pickup tanker or a milk
transport tank and their appurtenances are cleaned and sanitized prior to being
used the first time, after each use thereafter, and each time 72 hours has
elapsed since the last cleaning and sanitizing treatment;
12. Ensure that multiple milk pickups from dairy farms occur
during a 24-hour period without washing and sanitizing the farm bulk milk
pickup tanker only if a maximum of two hours elapses between the time of the
last delivery and start of the next milk pickup;
13. Pickup Pick up any milk in a farm bulk milk
pickup tanker or milk transport tank only if there exists a wash and sanitize
record for the farm bulk milk pickup tanker or milk transport tank documenting
that the tank has been washed and sanitized within the past 72 hours;
14. Install and use clamps on each milk pickup hose that are
easily dismantled by hand without the use of tools;
15. Identify and maintain each farm bulk milk pickup tanker or
milk transport tank with the identification numbers and letters assigned to
each farm bulk milk pickup tanker or milk transport tank by the state
regulatory agency. The identification shall be affixed to the left rear
bulkhead of the tanker;
16. Provide a suitable enclosure in the rear milk hose or
sample compartment of each farm bulk milk pickup tanker for storing inspection
sheets capable of protecting the inspection sheets from excessive moisture,
dust, soil, or light that might damage or render the inspection sheets
illegible and so they will be available to any state or federal regulatory
agent wherever the farm bulk milk pickup tanker might deliver;
17. Provide a suitable enclosure located within three feet of
the tank outlet valve or located on top of one of the rear wheel fenders for
each milk transport tank for storing inspection sheets capable of protecting
the inspection sheets from excessive moisture, dust, soil, or light that might
damage or render the inspection sheets illegible and so they will be available
to any state or federal regulatory agent wherever the milk transport tank might
deliver;
18. Completely empty the farm bulk cooling or holding tank
each time that milk is picked up;
19. Store the three most recent inspection reports for each
farm bulk milk pickup tanker or transport tank in the protected enclosure
provided on each farm bulk milk pickup tanker or transport tank at all times;
and
20. Provide a means to lock or seal each opening into a bulk
milk pickup tanker or milk transport tank for security purposes.
B. When picking up and transporting any milk in a bulk milk
pickup tanker each bulk milk hauler shall:
1. Practice good hygiene, maintain a neat and clean
appearance, and abstain from using tobacco products in any milkhouse;
2. Conduct all pickup and handling practices to prevent
contamination of any milk contact surface;
3. Pass the milk transfer hose through the hose port and
remove the cap from the transfer milk hose and set it where it will not become
contaminated and then attach the transfer milk hose to the tank outlet valve;
4. Wash his hands thoroughly and dry his hands with a clean
single-service towel or electric forced air hand dryer immediately prior to
measuring or sampling the milk in the tank;
5. Examine the milk in the tank by sight and smell for any off
odor or any other abnormalities that would render the milk unacceptable and
reject the milk if necessary;
6. Record the milk producer's name, milk producer's
identification number, the date and time of pickup, the temperature of the
milk, the measuring rod reading, the poundage, the name of the purchasing
organization, and the signature of the bulk milk hauler on the producer's
weight ticket;
7. Check the temperature of the milk in each farm bulk cooling
or holding tank at least once a month with an accurately calibrated pocket
thermometer after it has been properly sanitized;
8. Turn off the milk tank agitator if it is running when they
arrive he arrives at the milkhouse or milkroom and allow the surface
of the milk to become quiescent;
9. Carefully insert the measuring rod, after it has been wiped
dry with a single-service towel, into the tank and then read the measurement.
Each bulk milk hauler shall repeat this procedure until two identical
measurements are obtained and then shall record the measurement on the weight
ticket;
10. Agitate the milk in each tank holding two thousand 2,000
gallons or less of milk a minimum of five minutes before collecting any
milk sample;
11. Agitate the milk in each tank holding more than two
thousand 2,000 gallons of milk a minimum of ten 10
minutes before collecting any milk sample;
12. While the tank is being agitated, bring the sample
container, dipper, dipper container, and sanitizing agent, or single service
sampling tubes into the milkhouse aseptically;
13. While the tank is being agitated, remove the cap from the
tank outlet valve and examine for milk deposits or foreign matter and then
sanitize if necessary;
14. Remove the sample dipper or sampling device from the
sanitizing solution and rinse it in the milk from the tank at least twice
before collecting any official milk sample;
15. Collect two representative samples from each tank after
the milk has been properly agitated, transferring the milk from the sample
dipper to the sample container away from the tank opening to avoid spilling any
milk back into the tank, and filling the sample containers only three
quarters 3/4 full;
16. Rinse the sample dipper with water until it is free of
visible milk and replace it in its carrying container;
17. Close the cover or lid of the bulk tank;
18. Identify each milk sample with the producer's patron or
member number and the date of collection;
19. Collect at the first pickup for each load of milk two
temperature samples and identify the temperature samples with the date, time,
temperature of the milk, producer number, and name of the bulk milk hauler;
20. Place each milk sample collected immediately on ice in the
sample storage cooler;
21. After collection of milk samples, open the outlet valve
and start the pump to transfer the milk from the farm tank to the bulk milk
pickup tanker;
22. Turn off the agitator once the level of milk in the tank
has reached the level where over-agitation will occur;
23. Disconnect and cap the transfer hose after removing it
from the outlet valve of the tank;
24. Observe the walls and bottom of the tank for foreign
matter and extraneous material and record any objectionable observations on the
weight ticket;
25. Rinse the entire inside of the tank with warm water while
the tank outlet valve is open;
26. Use only sample containers and single-service sampling
tubes that comply with all the requirements contained in Standard Methods for
the Examination of Dairy Products, 16th 17th Edition, 1992
2004;
27. Cool and store all official milk samples to a temperature
of 40°F or cooler, but not frozen;
28. Provide sufficient ice and water or other coolant in the
sample storage cooler to maintain all milk samples at proper temperature;
29. Discard any milk that remains in the external transfer
system that exceeds 45°F including any milk in pumps, hoses, and air
elimination equipment or metering systems;
30. Protect samples from contamination and shall not
bury the tops of sample containers in ice or bury sample containers above the
milk level in the sample containers;
31. Keep all producer milk samples that represent the
commingled milk on the load with the load of milk until the load of milk has
been received by a milk plant, receiving station, or transfer station or if rejected
by a milk plant, receiving station, or transfer station until the milk samples
are collected for official laboratory testing to determine the disposition of
the load of milk; and
32. Deliver each bulk milk pickup tanker of commingled milk to
a milk plant, receiving station, or transfer station within 24 hours after the
last milk pickup on the route for the bulk milk pickup tanker.
C. When sampling any milk from a bulk milk pickup tanker or
transport tanker the dairy plant sampler shall:
1. Practice good hygiene, maintain a neat and clean
appearance, and abstain from using tobacco products in the receiving area;
2. Conduct all sampling and handling practices to prevent
contamination of any milk contact surface;
3. Wash his hands thoroughly and dry his hands with a clean
single-service towel or acceptable air dryer immediately prior to sampling the
milk in the tank;
4. Examine the milk in the tank by sight and smell for any off
odor or any other abnormalities that would classify the milk as unacceptable
and reject the milk if necessary;
5. Agitate for a period of time needed to blend the milk in
each compartment to a homogenous state using odor-free, pressurized, filtered
air or electrically driven stirring or recirculating equipment that has been properly
sanitized before sampling or receiving;
6. Check the temperature of the milk in each compartment with
a properly sanitized thermometer that has been checked against a standardized
thermometer at least once every six months and certified accurate;
7. Reject any milk that has a temperature above 45°F;
8. Bring the sample container, properly constructed sample
dipper, and sanitizing solution to the tanker aseptically after the milk is
properly agitated;
9. Remove the sample dipper or sampling device from the
sanitizing solution and rinse it in the milk from the tank at least twice
before collecting any official milk sample;
10. Collect at least one representative sample from each
compartment of the tanker, transferring the milk from the sample dipper to the
sample container away from the tank opening to avoid spilling any milk back
into the tank, and filling the sample container only three quarters full;
11. Rinse the sample dipper with water until it is free of
visible milk and replace it in its carrying container or storage container;
12. Close the cover or lid for each compartment of the bulk
milk tanker;
13. Identify each milk sample with the tanker number,
compartment if the tanker is equipped with more than one compartment, and the
date of collection;
14. Place each milk sample collected immediately on ice in a
sample storage cooler or deliver it to the laboratory for immediate analysis;
15. Attach the milk transfer hose to the outlet valve of the
milk tank truck and open the outlet valve of the milk tank truck before
starting the pump to transfer the milk from the bulk milk pickup tanker to the
milk plant storage facility or silo only after the collection of official milk
samples;
16. Turn off the agitator once the level of milk in the tank
has reached the level where over-agitation will occur;
17. Disconnect and cap the transfer hose after removing it
from the outlet valve of the tank;
18. Observe the walls and bottom of the tank for foreign
matter and extraneous material and record any objectionable observations on the
plant receiving log;
19. Rinse the entire inside of the tanker with warm water after
the tanker has been emptied and the external transfer system has been
disconnected while the tanker outlet valve is open;
20. Use only sample containers and single-service sampling
tubes that comply with all the requirements contained in Standard Methods for
the Examination of Dairy Products, 16th 17th Edition, 1992
2004;
21. Cool and store all official milk samples to a temperature
of 40°F or cooler, but not frozen;
22. Provide sufficient ice and water or other coolant in the
sample storage cooler to maintain all milk samples at proper temperature;
23. Protect samples from contamination and not bury tops of
sample containers in ice or bury samples above the milk level in the sample
containers;
24. Promptly deliver samples and sample data to the laboratory;
and
25. Discard any milk that remains in the external transfer
system that exceeds 45°F including any milk in pumps, hoses, air elimination
equipment, or metering systems.
D. Wash and sanitize records. Each bulk milk hauler
shall:
1. Ensure each bulk milk pickup tanker or milk transport tank
is properly cleaned and sanitized after unloading;
2. Ensure a cleaning and sanitizing tag is affixed to the
outlet valve of the bulk milk pickup tanker or milk transport tank after it is
washed;
3. Ensure when the bulk milk pickup tanker or milk transport
tank is next washed, the previous cleaning and sanitizing tag is removed and
stored at the location where the bulk milk pickup tanker or milk transport tank
was washed; and
4. Ensure the following information is recorded on the wash
and sanitize tag before it is attached to the outlet valve of the bulk milk
pickup tanker or milk transport tank:
a. Identification number of the bulk milk pickup tanker or
milk transport tank;
b. Date and time of day the bulk milk pickup tanker or milk
transport tank was cleaned and sanitized;
c. Location where the bulk milk pickup tanker or milk
transport tank was cleaned and sanitized; and
d. The signature of the person who cleaned and sanitized the
bulk milk pickup tanker or milk transport tank.
E. Wash and sanitize records. Each person who that
operates a milk plant, receiving station, or transfer station and each dairy
plant sampler responsible for sampling and receiving milk into a milk plant,
receiving station, or transfer station shall:
1. Ensure each bulk milk pickup tanker and milk transport tank
is properly cleaned and sanitized after unloading;
2. Ensure a cleaning and sanitizing tag is affixed to the
outlet valve of the bulk milk pickup tanker or milk transport tank after it is
washed;
3. Ensure when washing a bulk milk pickup tanker or milk
transport tank, the previous cleaning and sanitizing tag is removed and stored
at the location where the bulk milk pickup tanker or milk transport tank is
washed; and
4. Record the following information on the wash and sanitize
tag before it is attached to the outlet valve of the bulk milk pickup tanker or
milk transport tank:
a. Identification number of the bulk milk pickup tanker or
milk transport tank;
b. Date and time of day the bulk milk pickup tanker or milk
transport tank was cleaned and sanitized;
c. Location where the bulk milk pickup tanker or milk
transport tank was cleaned and sanitized; and
d. The signature of the person who cleaned and sanitized the
bulk milk pickup tanker or milk transport tank.
F. Labeling and shipping documents. Each bulk milk
hauler shall ensure that each shipping document or load manifest contains the
following information for each bulk milk pickup tanker or milk transport tank:
1. The shipper's name, address, and permit number;
2. The Interstate Milk Shipper Bulk Tank Unit identification
number for each Bulk Tank Unit on the load of milk or the Interstate Milk
Shipper listed Plant Number;
3. The milk hauler permit number if the milk hauler is not an
employee of the shipper;
4. The point of origin of the shipment;
5. The bulk milk pickup tanker or milk transport tank
identification number;
6. The name of the product;
7. The weight of the product;
8. The temperature of the product when loaded;
9. The date of shipment;
10. The name of the supervising regulatory agency at the point
of origin of shipment;
11. A statement as to whether the contents of the load are
raw, pasteurized, or in the case of cream, lowfat, or skim milk whether it has
been heat-treated;
12. The seal number on inlet, outlet, wash connections and
vents, if applicable; and
13. The grade of the product.
G. Protection of bulk milk and chain of custody of milk
samples. Each contract hauler, subcontract hauler, bulk milk hauler, and
operator of a bulk milk pickup tanker or milk transport tank shall:
1. Each contract hauler, subcontract hauler, bulk milk
hauler, and operator of a bulk milk pickup tanker or milk transport tank shall
ensure Ensure the proper protection of all milk and milk samples in
his custody. Each contract hauler, subcontract hauler, bulk milk hauler, and
operator of a bulk milk pickup tanker or milk transport tank shall seal or lock
each opening into a bulk milk pickup tanker or milk transport tank including
each manhole lid, vent, wash port, and door to the pump housing and sample
storage box prior to leaving the bulk milk pickup tanker or milk transport tank
unattended.;
2. Each contract hauler, subcontract hauler, bulk milk hauler,
and operator of a bulk milk pickup tanker or milk transport tank shall inspect
Inspect the condition of the seals and locks placed on each opening into
the bulk milk pickup tanker or milk transport tank upon his return after an
absence to determine if the seals or locks have been tampered with.;
3. Each contract hauler, subcontract hauler, bulk milk
hauler, and operator of a bulk milk pickup tanker or milk transport tank shall
report Report immediately to the state regulatory authority
instances of tampering with the seals or locks.; and
4. Each contract hauler, subcontract hauler, bulk milk
hauler, and operator of a bulk milk pickup tanker or milk transport tank shall
hold Hold a valid permit issued by the state regulatory authority
for the collection of milk samples prior to collecting or transporting any milk
or milk samples.
H. Notwithstanding the provisions of subdivisions A 4 and A 8
of this section for each contract hauler or subcontract hauler to provide a
sample dipper and approved sanitizer for the sample dipper container, the
sample dipper, sample dipper container, and approved sanitizer may be
provided and stored in the milkroom accessible to the contract hauler or
subcontract hauler by the person operating the dairy farm where the contract hauler
or subcontract hauler is picking up the milk.
2VAC5-501-90. Sanitation requirements for a milk tank truck
cleaning facility.
Each person who that operates a milk tank truck
cleaning facility permit shall:
1. Provide floors constructed of concrete or equally
impervious material that are easily cleanable, smooth, properly sloped, and
provided with trapped floor drains and kept in good repair;
2. Provide walls and ceilings with a smooth, washable,
light-colored surface and kept in good repair;
3. Provide effective means to prevent the access of flies and
rodents;
4. Provide solid doors or glazed windows for each opening to
the outside and keep the doors and windows closed during dusty weather;
5. Provide lighting of at least 20 foot-candles measured in
all work areas;
6. Provide ventilation sufficient to prevent condensation and
odors;
7. Provide a toilet room fitted with tightly-fitting
self-closing doors, kept clean and in good repair, well-ventilated and lighted
and that does not open directly into any room in which milk or milk products
are processed or milk product contact-surfaces, utensils and equipment are
washed;
8. Dispose of all sewage and other wastes in a sanitary
manner;
9. Provide hot and cold running water from a supply that is
properly located, protected, and operated, and shall be easily accessible,
adequate, and of a safe and sanitary quality;
10. Provide hand-washing facilities with hot and cold running
water, soap, and individual sanitary towels or other approved hand-drying
devices and keep the hand-washing facilities clean and in good repair;
11. Provide and maintain an effective insect and rodent
control program and shall keep the milk tank truck cleaning facility neat and
clean;
12. Provide only sanitary piping, fittings, and connections
that are constructed to be smooth, impervious, corrosion-resistant, nontoxic,
easily cleanable, and manufactured from material that is approved for food
contact surfaces;
13. Provide and use only stainless steel piping complying with
the American Iron and Steel Institute (AISI) 300 series as published in the
Iron and Steel Society's Steel Products Manual for Manual:
Stainless Steels, dated March 1999;
14. Provide only sanitary piping, fittings, and connections
that are in good repair and constructed for ease of cleaning;
15. Provide and use only plastic, rubber, or rubber-like
materials made from approved food contact-grade materials that are relatively
inert, and resistant to scratching, scoring, and damage from cleaning
compounds;
16. Clean and sanitize before each use the product-contact
surfaces of utensils and equipment used in the transportation of any milk or
food;
17. Attach a wash tag to the outlet valve of the tanker
showing the date, time, place, and signature of the employee who washed the
bulk milk pickup tanker or milk transport tank after the milk tank truck has
been cleaned and sanitized;
18. Store and transport all clean and sanitized utensils and
equipment to assure complete draining and protection from contamination before
use;
19. Store all single-service containers, utensils, and
materials in a sanitary manner in a clean dry place until used;
20. Store, handle, and use poisonous or toxic materials to
preclude the contamination of any milk product contact-surfaces of equipment
and utensils;
21. Ensure that his employees wash their hands
thoroughly before commencing cleaning functions and as may be required to
remove soil and contamination;
22. Allow an employee to resume work after visiting the toilet
room only after that employee has thoroughly washed his hands;
23. Ensure that each of his employees employee
engaged in the handling of milk product contact-surfaces, equipment, and
utensils wears clean outer garments, adequate hair covering, and refrains from
using any tobacco products; and
24. Keep the surroundings of the milk tank truck cleaning
facility neat, clean, and free from conditions that may attract flies, insects,
or rodents.
2VAC5-501-110. Regulation superseded. (Repealed.)
This chapter supersedes 2VAC5-500, Rules and Regulations
Governing the Cooling, Storing, Sampling and Transporting of Milk or Milk
Samples from the Farm to the Processing Plant or Laboratory, and is based upon
a Notice of Intended Regulatory Action published in the Virginia Register of
Regulations for June 4, 2001 at page 2704 under "Title 2.
Agriculture."
NOTICE: The following
forms used in administering the regulation were filed by the agency. The forms
are not being published; however, online users of this issue of the Virginia
Register of Regulations may click on the name of a form with a hyperlink to
access it. The forms are also available from the agency contact or may be
viewed at the Office of the Registrar of Regulations, General Assembly
Building, 2nd Floor, Richmond, Virginia 23219.
FORMS (2VAC5-501)
Application
for a Dairy Farm Permit, ODF-DS-100 (rev. 6/2012)
Dairy
Farm Inspection Report, ODF-DS-102 (rev. 2/2006)
Guide
for the Submission of Plans for Milking Operations, ODF-DS-104 (rev. 2/2015)
DOCUMENTS INCORPORATED BY REFERENCE (2VAC5-501)
3-A Sanitary Standards for Stainless Steel Automotive
Transportation Tanks for Bulk Delivery and Farm Pick-Up Service, Number 05-15,
eff. November 24, 2002, 3-A Sanitary Standards, Inc. Incorporated, 6888
Elm Street, Suite 2D, McLean, Virginia 22101, www.3-a.org
3-A Sanitary Standards, effective as of November 20, 2001,
3-A Sanitary Standards, Incorporated.
3-A
Sanitary Standards for Farm Milk Cooling and Holding Tanks, Number 13-11,
eff. July 23, 2012, 3-A Sanitary Standards, Incorporated, 6888 Elm
Street, Suite 2D, McLean, Virginia 22101, www.3-a.org
3-A Sanitary Standards for Farm Milk Storage Tanks, Number
30-01, eff. September 9, 1984, 3-A Sanitary Standards, Incorporated, 6888
Elm Street, Suite 2D, McLean, Virginia 22101, www.3-a.org
UL
Rated NEMA 4x Enclosure Definition as published in ANSI/NEMA 250, Enclosures
for Electrical Equipment (1000 Volts Maximum), ANSI Approval Date August
30, 2001 December 29, 2014, American Society of Mechanical Engineers.
Standard
Methods for the Examination of Dairy Products, 16th 17th
Edition, 1992 2004, American Public Health Association.
American Iron & Steel Institute (AISI) 300 Series as
published in Steel Products Manual -: Stainless Steels, March
1999, Iron and Steel Society., 186 Thorn Hill Road, Warrendale,
Pennsylvania 15086 www.iom3.org/iron-steel-society
VA.R. Doc. No. R16-4567; Filed June 21, 2016, 12:44 p.m.
TITLE 4. CONSERVATION AND NATURAL RESOURCES
BOARD OF GAME AND INLAND FISHERIES
Final Regulation
REGISTRAR'S NOTICE: The
Board of Game and Inland Fisheries is claiming an exemption from the
Administrative Process Act pursuant to § 2.2-4002 A 3 of the Code of
Virginia when promulgating regulations regarding the management of wildlife.
Title of Regulation: 4VAC15-20. Definitions and
Miscellaneous: In General (adding 4VAC15-20-230; repealing
4VAC15-20-80).
Statutory Authority: § 29.1-501 of the Code of Virginia.
Effective Date: July 1, 2016.
Agency Contact: Phil Smith, Regulatory Coordinator,
Department of Game and Inland Fisheries, 7870 Villa Park Drive, Suite 400,
Henrico, VA 23228, telephone (804) 367-8341 or email
phil.smith@dgif.virginia.gov.
Summary:
The amendments (i) repeal requirements regarding execution
of a certificate for a resident license by the licensee and (ii) prescribe
aluminum or purple as the color of paint to be used for posting land to
prohibit hunting, fishing, or trapping without the written permission of the
landowner.
4VAC15-20-80. Certificate on hunting, trapping and fishing
license to be executed by licensee. (Repealed.)
No state or county resident license to hunt, trap or fish
in or on the lands or inland waters of this Commonwealth shall be deemed to be
issued until the certificate printed on the reverse side of that license shall
have been executed by the named licensee. For those licenses issued by
telephone or electronic media agent pursuant to § 29.1-327 B of the Code
of Virginia, the license shall be deemed issued when the license authorization
number is put on paper and the paper is signed by the designated licensee and
shall remain effective only until the permanent license, for which the number
was issued, is received by the licensee.
4VAC15-20-230. Color of paint prescribed for posting land.
The color of paint prescribed for posting land in
accordance with § 18.2-134.1 of the Code of Virginia shall be aluminum or
purple.
VA.R. Doc. No. R16-4689; Filed June 28, 2016, 4:01 p.m.
TITLE 4. CONSERVATION AND NATURAL RESOURCES
MARINE RESOURCES COMMISSION
Emergency Regulation
Title of Regulation: 4VAC20-1090. Pertaining to
Licensing Requirements and License Fees (amending 4VAC20-1090-30).
Statutory Authority: §§ 28.2-201 and 28.2-210 of the
Code of Virginia.
Effective Dates: July 1, 2016, through July 30, 2016.
Agency Contact: Jennifer Farmer, Regulatory Coordinator,
Marine Resources Commission, 2600 Washington Avenue, 3rd Floor, Newport News,
VA 23607, telephone (757) 247-2248, or email jennifer.farmer@mrc.virginia.gov.
Preamble:
Pursuant to § 28.2-226.2 of the Code of Virginia the
amendment separates the five crab pot recreational license into two categories,
one with a terrapin excluder device ($36) and one without such device ($46).
4VAC20-1090-30. License fees.
The following listing of license fees applies to any person
who purchases a license for the purposes of harvesting for commercial purposes,
or fishing for recreational purposes, during any calendar year. The fees listed
below include a $1.00 agent fee.
EDITOR'S NOTE:
Subdivisions 1 through 10 and 12 through 16 of 4VAC20-1090-30 are not amended;
therefore, the text of those subdivisions is not set out.
11. COMMERCIAL GEAR FOR RECREATIONAL USE
|
Up to five crab pots with a terrapin excluder device
|
$36.00
|
Up to five crab pots without a terrapin excluder device
|
$46.00
|
Crab trotline (300 feet maximum)
|
$10.00
|
One crab trap or crab pound
|
$6.00
|
One gill net up to 300 feet in length
|
$9.00
|
Fish dip net
|
$7.00
|
Fish cast net
|
$10.00
|
Up to two eel pots
|
$10.00
|
VA.R. Doc. No. R16-4787; Filed June 29, 2016, 3:02 p.m.
TITLE 4. CONSERVATION AND NATURAL RESOURCES
MARINE RESOURCES COMMISSION
Final Regulation
REGISTRAR'S NOTICE: Pursuant to § 28.2-106.2 of the Code of Virginia, the provisions of the Administrative Process Act (§ 2.2-4000 et seq. of the Code of Virginia) and §§ 28.2-209 through 28.2-215 do not apply to regulations promulgated under that section.
Title of Regulation: 4VAC20-1320. Pertaining to Establishment of Restricted Area - Maritime Administration James River Reserve Fleet (adding 4VAC20-1320-10 through 4VAC20-1320-50).
Statutory Authority: § 28.2-106.2 of the Code of Virginia.
Effective Date: June 30, 2016.
Agency Contact: Jennifer Farmer, Regulatory Coordinator, Marine Resources Commission, 2600 Washington Avenue, 3rd Floor, Newport News, VA 23607, telephone (757) 247-2248 or email jennifer.farmer@mrc.virginia.gov.
Summary:
The purpose of the establishment of this regulation is to enhance the physical security of the James River Reserve Fleet as part of a comprehensive plan to protect the public, environment, and economic interests from sabotage and other subversive acts, accidents, or incidents of a similar nature. This regulation delineates an area within an undefined area already designated by the federal government under 33 CFR 162.270, Restricted areas in vicinity of Maritime Administration Reserve Fleets, and provides the Virginia Marine Police the authority to enforce Virginia law that prohibits entrance into prohibited restricted areas.
CHAPTER 1320
PERTAINING TO ESTABLISHMENT OF RESTRICTED AREA - MARITIME ADMINISTRATION JAMES RIVER RESERVE FLEET
4VAC20-1320-10. Purpose.
The purpose of this chapter is to enhance the physical security of the James River Reserve Fleet as part of a comprehensive plan to protect the public, environment, and economic interests from sabotage and other subversive acts, accidents, or incidents of a similar nature.
This regulation delineates an area within an undefined area already designated by the federal government under 33 CFR 162.270 and provides the Virginia Marine Police the authority to enforce Virginia law that prohibits entrance into prohibited restricted areas.
4VAC20-1320-20. Definitions.
The following words when used in this chapter shall have the following meanings unless the context clearly indicates otherwise:
"Restricted area" means those waters within an area beginning at latitude 37º08.4999992' N, longitude 76º38.4799994' W; thence to latitude 37º07.1885596' N, longitude76º38.4395503 W; thence to latitude 37º06.9585351' N, longitude 76º38.4331102' W; thence to latitude 37º06.4202049' N, longitude 76º38.4158624' W; thence to latitude 37º06.1150372' N, longitude 76º38.5271810' W; thence to latitude 37º06.6400002' N, longitude 76º39.1899998' W; thence to latitude 37º07.8999983' N, longitude 76º39.3400007' W; thence to latitude 37º08.4999986' N, longitude 76º38.6299996' W; thence to latitude 37º08.4999992' N, longitude 76º38.4799994' W, being the point of beginning.
4VAC20-1320-30. Prohibitions.
No vessel or other watercraft, except those owned or controlled by the United States government or the Virginia Marine Police, shall cruise or anchor within the restricted area as defined in 4VAC20-1320-20 any closer than 500 feet of any reserve fleet unit or units unless specific permission to do so has first been granted in each case by the Maritime Administration James River Reserve Fleet.
4VAC20-1320-40. Penalty.
As set forth in § 28.2-106.2 D of the Code of Virginia, any person violating any provision of this chapter shall be guilty of a Class I misdemeanor.
4VAC20-1320-50. Duration of regulation.
This regulation will remain in effect until the federal rule pertaining to this restricted area expires.
VA.R. Doc. No. R16-4794; Filed June 30, 2016, 12:13 p.m.
TITLE 8. EDUCATION
STATE BOARD OF EDUCATION
Final Regulation
REGISTRAR'S NOTICE: The
State Board of Education is claiming an exclusion from Article 2 of the
Administrative Process Act in accordance with § 2.2-4006 A 4 a of the Code
of Virginia, which excludes regulations that are necessary to conform to
changes in Virginia statutory law where no agency discretion is involved. The
State Board of Education will receive, consider, and respond to petitions by
any interested person at any time with respect to reconsideration or revision.
Title of Regulation: 8VAC20-70. Regulations Governing
Pupil Transportation (amending 8VAC20-70-460).
Statutory Authority: §§ 22.1-16, 22.1-176, and 22.1-177
of the Code of Virginia.
Effective Date: August 10, 2016.
Agency Contact: Melissa Luchau, Director for Board
Relations, Department of Education, P.O. Box 2120, 101 North 14th Street, 25th
Floor, Richmond, VA 23219, telephone (804) 225-2924, FAX (804) 225-2524, or
email melissa.luchau@doe.virginia.gov.
Summary:
To comport with Chapter 559 of the 2015 Acts of Assembly,
the amendments permit a local school board to sell or transfer its school buses
to another school division or purchase a used bus from another school division
or a school bus dealer as long as the bus (i) conforms to the State Board of
Education's construction and design specifications in effect at the time of
manufacture, (ii) has a valid Virginia State Police inspection, and (iii) is
not older than 15 model years at the time of sale, transfer, or purchase.
Part IV
General Requirements for School Buses in Virginia
8VAC20-70-460. Specifications.
It is the intent of the Board of Education to accommodate new
equipment and technology that will better facilitate the safe and efficient
transportation of students. When a new technology, piece of equipment, or
component is desired to be applied to a school bus, it must have the approval
of the Department of Education and must meet the following criteria:
1. The technology, equipment, or component shall not compromise
the effectiveness or integrity of any major safety system.
2. The technology, equipment, or component shall not diminish
the safety of the interior of the bus.
3. The technology, equipment, or component shall not create
additional risk to students who are boarding or exiting the bus or are in or
near the school bus loading zone.
4. The technology, equipment, or component shall not require
undue additional activity or responsibility for the driver.
5. The technology, equipment, or component shall generally
increase efficiency or safety, or both, of the bus, generally provide for a
safer or more pleasant experience for the occupants and pedestrians in the
vicinity of the bus, or shall generally assist the driver and make his many
tasks easier to perform.
School buses and school activity buses purchased new
must conform to the specifications relative to construction and design
effective on the date of the initial procurement. Any variation from the
specifications, in the form of additional equipment or changes in style of
equipment, without prior approval of the Department of Education, is
prohibited. The Department of Education shall issue specifications and
standards for public school buses to reflect desired technology or safety
improvements for the then current model year.
A local school board may sell or transfer any of its
school buses or school activity buses to another school division or purchase a
used bus from another school division or a school bus dealer as long as the
school bus or school activity bus conforms to the specifications relating to
construction and design in effect on the date of manufacture. The bus must also
have a valid Virginia State Police inspection and may not be older than 15
model years at the time of sale, transfer, or purchase.
VA.R. Doc. No. R16-4577; Filed June 17, 2016, 2:12 p.m.
TITLE 12. HEALTH
STATE BOARD OF HEALTH
Notice of Extension of Emergency Regulation
Titles of Regulations: 12VAC5-71. Regulations
Governing Virginia Newborn Screening Services (amending 12VAC5-71-30, 12VAC5-71-150; adding
12VAC5-71-200 through 12VAC5-71-260).
12VAC5-191. State Plan for the Children with Special Health
Care Needs Program (amending 12VAC5-191-260).
Statutory Authority: §§ 32.1-12, 32.1-65.1, and 32.1-67
of the Code of Virginia.
Expiration Date Extended Through: December 22, 2016.
The Governor has approved the State Board of Health request to
extend the expiration date of the above-referenced emergency regulation for six
months as provided for in § 2.2-4011 D of the Code of Virginia. Therefore,
the emergency regulation will continue in effect through December 22, 2016. The
emergency regulation relates to screening for critical congenital heart disease
and permitting the Virginia Department of Health to collect information via the
Virginia Congenital Anomalies Reporting and Education System (VaCARES)
reporting system. The emergency regulation was published in 31:11 VA.R. 942-946 January 26, 2015.
Agency Contact: Dev Nair, Director, Division of Policy
and Evaluation, Department of Health, 109 Governor Street, Richmond, VA 23219,
telephone (804) 864-7662, FAX (804) 864-7647, or email
dev.nair@vdh.virginia.gov.
VA.R. Doc. No. R15-4176; Filed June 17, 2016, 5:22 p.m.
TITLE 12. HEALTH
STATE BOARD OF HEALTH
Notice of Extension of Emergency Regulation
Titles of Regulations: 12VAC5-71. Regulations
Governing Virginia Newborn Screening Services (amending 12VAC5-71-30, 12VAC5-71-150; adding
12VAC5-71-200 through 12VAC5-71-260).
12VAC5-191. State Plan for the Children with Special Health
Care Needs Program (amending 12VAC5-191-260).
Statutory Authority: §§ 32.1-12, 32.1-65.1, and 32.1-67
of the Code of Virginia.
Expiration Date Extended Through: December 22, 2016.
The Governor has approved the State Board of Health request to
extend the expiration date of the above-referenced emergency regulation for six
months as provided for in § 2.2-4011 D of the Code of Virginia. Therefore,
the emergency regulation will continue in effect through December 22, 2016. The
emergency regulation relates to screening for critical congenital heart disease
and permitting the Virginia Department of Health to collect information via the
Virginia Congenital Anomalies Reporting and Education System (VaCARES)
reporting system. The emergency regulation was published in 31:11 VA.R. 942-946 January 26, 2015.
Agency Contact: Dev Nair, Director, Division of Policy
and Evaluation, Department of Health, 109 Governor Street, Richmond, VA 23219,
telephone (804) 864-7662, FAX (804) 864-7647, or email
dev.nair@vdh.virginia.gov.
VA.R. Doc. No. R15-4176; Filed June 17, 2016, 5:22 p.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Final Regulation
Title of Regulation: 12VAC30-20. Administration of
Medical Assistance Services (amending 12VAC30-20-500 through 12VAC30-20-560).
Statutory Authority: § 32.1-325 of the Code of Virginia;
42 USC § 1396 et seq.
Effective Date: August 10, 2016.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, Policy Division, 600 East Broad
Street, Suite 1300, Richmond, VA 23219, telephone (804) 371-4300, FAX (804)
786-1680, or email emily.mcclellan@dmas.virginia.gov.
Summary:
The amendments (i) address the manner in which alleged
deficiencies in case summaries can be resolved and the means by which
documentation can be transmitted in an informal appeal; (ii) clarify and adjust
timelines and filing specifications, for example an extension of a 45-day
limitation in which the hearing officer must conduct a formal hearing if agreed
to by all parties and delivery using electronic means are added; and (iii)
update and clarify the department's authority to take administrative action to
dismiss untimely, unauthorized, or insufficient appeal requests.
Summary of Public Comments and Agency's Response: A
summary of comments made by the public and the agency's response may be
obtained from the promulgating agency or viewed at the office of the Registrar
of Regulations.
Part XII
Provider Appeals
12VAC30-20-500. Definitions.
The following words, and terms when used in
this part, shall have the following meanings:
"Administrative dismissal" means a dismissal
that requires only the issuance of a decision with appeal rights but does not
require the submission of a case summary or any further proceeding.
"Day" means a calendar day unless otherwise stated.
"DMAS" means the Virginia Department of Medical
Assistance Services or its agents or contractors.
"Hearing officer" means an individual selected by
the Executive Secretary of the Supreme Court of Virginia to conduct the formal
appeal in an impartial manner pursuant to §§ 2.2-4020 and 32.1-325.1 of
the Code of Virginia and this part.
"Informal appeals agent" means a DMAS employee who
conducts the informal appeal in an impartial manner pursuant to §§ .2-4019
and 32.1-325.1 of the Code of Virginia and this part.
"Last known address" means the provider's
physical or electronic correspondence address on record in the DMAS Medicaid
Management Information System as of the date DMAS transmits an item to the
provider or the address of the provider's counsel of record. Nothing herein
shall prevent DMAS and the provider from agreeing in writing during the course
of an audit or an appeal to use an alternative location for the transmittal of
an item or items related to the audit or the appeal.
"Provider" means an individual or entity that has a
contract with DMAS to provide covered services and that is not operated by the
Commonwealth of Virginia.
"Transmit" means to send by means of the United
States mail, courier or other hand delivery, facsimile, electronic mail, or electronic
submission.
12VAC30-20-520. Provider appeals: general provisions.
A. This part governs all DMAS informal and formal provider
appeals and shall supersede supersedes any other provider appeals
regulations.
B. A provider may appeal any DMAS action that is subject to
appeal under the Virginia Administrative Process Act (§ 2.2-4000 et seq.
of the Code of Virginia), including DMAS' interpretation and application of
payment methodologies. A provider may not appeal the actual payment
methodologies.
C. DMAS shall mail transmit all items to the
last known address of the provider. It is presumed that DMAS mails transmits
items on the date noted on the item. It is presumed that providers receive
items mailed transmitted by United States mail to their last known
address within three days after DMAS mails transmits the item by
United States mail. It is presumed that providers receive items transmitted by
[ facsimile, ] electronic mail [ , ] or [ facsimile
to their last known other ] electronic [ mail
address of facsimile number submission ] on the
date transmitted. It is presumed that [ the providers
receive ] items [ are received upon
transmitted by courier or other hand delivery ] the date [ and
time ] of delivery to the provider's last known address [ by
a courier ]. These presumptions in this section shall apply
unless the provider, through evidence beyond a mere denial of receipt,
introduces evidence sufficient to rebut the presumption. If a provider requests
a copy of an item, the transmittal date for the item remains the date
originally noted on the item, and not the date that the copy of the requested
item is transmitted. A provider's failure to accept delivery of an item
transmitted by DMAS, or a provider's failure to open an item upon receipt,
shall not result in an extension of any of the timelines established by this
part.
D. Whenever DMAS or a provider is required to file a
document, the document shall be considered filed when it is date stamped by the
DMAS Appeals Division in Richmond, Virginia.
E. Whenever the last day specified for the filing of any
document or the performance of any other act falls on a day on which DMAS is
officially closed for the full or partial day, the time period shall be
extended to the next day on which DMAS is officially open.
F. Conferences and hearings shall be conducted at DMAS' main
office in Richmond, Virginia, or at such other place as agreed to upon
in writing by the parties DMAS, the provider, and the informal
appeals agent for informal appeals. For formal appeals, this agreement shall be
between DMAS, the provider, and the hearing officer.
G. Whenever DMAS or a provider is required to attend a
conference or hearing, failure by one of the parties to attend the conference
or hearing shall result in dismissal of the appeal in favor of the other party.
H. DMAS shall reimburse a provider for reasonable and
necessary attorneys' fees and costs associated with an informal or formal administrative
appeal if the provider substantially prevails on the merits of the appeal and
DMAS' position is not substantially justified, unless special circumstances
would make an award unjust. In order to substantially prevail on the merits of
the appeal, the provider must be successful on more than 50% of the dollar
amount involved in the issues identified in the provider's notice of appeal.
I. Any document that is filed with the DMAS Appeals
Division after 5 p.m. [ Eastern Time shall be date stamped on the
next day DMAS is officially open. Any document that is filed with the DMAS
Appeals Division after 5 p.m. ] Eastern Time on the due date shall
be untimely.
12VAC30-20-540. Informal appeals.
A. Providers appealing a DMAS decision shall file a
written notice of informal appeal with the DMAS Appeals Division within 30 days
of the provider's receipt of the decision. Notice of informal appeal.
1. Providers appealing the termination or denial of
their Medicaid agreement pursuant to § 32.1-325 [ D E ]
of the Code of Virginia shall file a written notice of informal appeal
with the DMAS Appeals Division within 15 days of the provider's receipt of the
notice of termination or denial.
2. Providers appealing adjustments to a cost report
shall file a written notice of informal appeal with the DMAS Appeals Division
within 90 days of the provider's receipt of the notice of program
reimbursement. The written notice of informal appeal shall identify the
issues being appealed, adjustments, or items that the provider is
appealing.
3. Providers appealing all other DMAS decisions shall file
a written notice of informal appeal with the DMAS Appeals Division within 30
days of the provider's receipt of the decision. The written notice of informal
appeal shall identify each adjustment, patient, service date, or other disputed
matter that the provider is appealing.
B. Administrative
dismissals.
1. Failure to timely file a written notice of
informal appeal within 30 days of receipt of the decision or within 90 days
of receipt of the notice of program reimbursement shall result in dismissal of
the appeal. Failure to file a written notice of informal appeal for termination
or denial of a Medicaid agreement pursuant to § 32.1-325 D of the Code of
Virginia within 15 days of receipt of the notice of termination or denial shall
result in dismissal of the appeal with the information required by
subdivision A 2 or A 3 of this section shall result in an administrative
dismissal.
2. A representative, billing company, or other third-party
entity filing a written notice of appeal on behalf of a provider shall submit
to DMAS, at the time of filing or upon request, a written authorization to act
on the provider's behalf, signed by the provider. The authorization shall
reference the specific adverse action or actions being appealed including, if
applicable, each patient's name and date of service. Failure to submit a
written authorization as specified in this subdivision shall result in an
administrative dismissal. This requirement shall not apply to an appeal filed
by a Virginia licensed attorney.
3. If a provider has not exhausted any applicable DMAS or
contractor reconsideration or review process or contractor's internal appeals
process that the provider is required to exhaust before filing a DMAS informal
appeal, the provider's written notice of informal appeal shall be administratively
dismissed.
4. If DMAS has not issued a decision with appeal rights,
the provider's attempt to file a written notice of informal appeal, prior to
the issuance of a decision by DMAS that has appeal rights, shall be
administratively dismissed.
B. C. Written case summary.
1. DMAS shall file a written case summary with the DMAS
Appeals Division within 30 days of the filing of the provider's notice of
informal appeal. DMAS and shall mail transmit
a complete copy of the case summary to the provider on the same day that the
case summary is filed with the DMAS Appeals Division.
The case summary shall address each adjustment, patient,
service date, or other disputed matter and shall state DMAS' position for each
adjustment, patient, service date, or other disputed matter. The case summary
shall contain the factual basis for each adjustment, patient, service date, or
other disputed matter and any other information, authority, or documentation
DMAS relied upon in taking its action or making its decision. 2. For
each adjustment, patient, and service date or other disputed matter identified
by the provider in its notice of informal appeal, the case summary shall
explain the factual basis upon which DMAS relied in taking its action or making
its decision and identify any authority or documentation upon which DMAS relied
in taking its action or making its decision.
3. Failure to file a written case summary with the DMAS
Appeals Division in the detail specified within 30 days of the filing of the
provider's notice of informal appeal within 30 days of the filing of the
written notice of informal appeal shall result in dismissal in favor of the
provider on those issues not addressed in the detail specified.
4. The provider shall have 12 days following the due date
of the case summary to file with the DMAS Appeals Division and transmit to the
author of the case summary a written notice of all alleged deficiencies in the
case summary that the provider knows, or reasonably should know, exist. Failure
of the provider to timely file a written notice of deficiency with the DMAS
Appeals Division shall be deemed a waiver of all deficiencies, alleged or
otherwise, with the case summary.
5. Upon timely receipt of the provider's notice of
deficiency, DMAS shall have 12 days to address the alleged deficiency or
deficiencies. If DMAS does not address the alleged deficiency or does not
address the alleged deficiency to the provider's satisfaction, the alleged
deficiency or deficiencies shall become an issue to be addressed by the
informal appeals agent as part of the informal appeal decision.
6. The informal appeals agent shall make a determination as
to each deficiency that is alleged by the provider as set forth in this subsection.
In making that determination, the informal appeals agent shall determine
whether the alleged deficiency is such that it could not reasonably be
determined from the case summary the factual basis and authority for the DMAS
action, relating to the alleged deficiency, so as to require a dismissal in
favor of the provider on the issue or issues to which the alleged deficiency
pertains.
C. D. Conference.
1. The informal appeals agent shall conduct the
conference within 90 days from the filing of the notice of informal appeal. If
DMAS and, the provider, and the informal appeals agent
agree, the conference may be conducted by way of written submissions. If the
conference is conducted by way of written submissions, the informal appeals
agent shall specify the time within which the provider may file written
submissions, not to exceed 90 days from the filing of the notice of informal
appeal. Only written submissions filed within the time specified by the
informal appeals agent shall be considered.
D. 2. The conference may be recorded at the
discretion of the informal appeals agent and solely for the convenience of
the informal appeals agent. Since Because the conference is not
an adversarial or evidentiary proceeding, recordings shall not be made part
of the administrative record and shall not be made available to anyone other
than the informal appeals agent no other recordings or transcriptions
shall be permitted. Any recordings made for the convenience of the informal
appeals agent shall not be released to DMAS or to the provider.
E. 3. Upon completion of the conference, the
informal appeals agent shall specify the time within which the provider may
file additional documentation or information, if any, not to exceed 30 days.
Only documentation or information filed within the time specified by the
informal appeals agent shall be considered.
F. E. Informal appeals decision. The informal
appeal decision shall be issued within 180 days of receipt of the notice of
informal appeal.
F. Remand. Whenever an informal appeal is required
pursuant to a remand by court order, final agency decision, agreement of the
parties, or otherwise, all time periods set forth in this section shall begin
to run effective with the date that the document containing the remand is
date-stamped by the DMAS Appeals Division in Richmond, Virginia.
12VAC30-20-560. Formal appeals.
A. Any A provider appealing a DMAS informal
appeal decision shall file a written notice of formal appeal with the DMAS
Appeals Division within 30 days of the provider's receipt of the informal
appeal decision. The notice of formal appeal shall identify the issues being
appealed each adjustment, patient, service date, or other disputed
matter that the provider is appealing. Failure to file a written notice of
formal appeal in the detail specified within 30 days of receipt of the
informal appeal decision shall result in dismissal of the appeal. Pursuant
to § 2.2-4019 A of the Code of Virginia, DMAS shall ascertain the fact basis
for decisions through informal proceedings unless the parties consent in
writing to waive such a conference or proceeding to go directly to a formal
hearing, and therefore only issues that were addressed pursuant to § 2.2-4019
shall be addressed in the formal appeal, unless DMAS and the provider consent
to waive the informal fact-finding process under § 2.2-4019 A of the Code
of Virginia.
B. DMAS and the provider shall exchange and file with the
hearing officer all documentary evidence on which DMAS or the provider relies
within 21 days of the filing of the notice of formal appeal. Only documents
filed within 21 days of the filing of the notice of formal appeal shall be
considered. DMAS and the provider shall file any objections to the
admissibility of documentary evidence within seven days of the filing of the
documentary evidence. Only objections filed within seven days of the filing of
the documentary evidence shall be considered. The hearing officer shall rule on
any objections within seven days of the filing of the objections. Documentary
evidence [ , objections to documentary evidence, opening briefs,
and reply briefs ].
1. [ Objections Documentary
evidence, objections ] to documentary evidence, opening briefs, and
reply briefs shall be filed with the DMAS Appeals Division on the date
specified in this subsection. The hearing officer shall only consider those
documents or pleadings that are filed within the required timeline. [ DMAS
and Simultaneous with filing, ] the [ provider
filing party ] shall [ also ] transmit
[ any required document a copy ] to the
other party and to the hearing officer [ on the date of filing ].
a. All documentary evidence upon which DMAS or the provider
relies shall be filed within 21 days of the filing of the notice of formal
appeal.
b. Any objections to the admissibility of documentary
evidence shall be filed within seven days of the filing of the documentary
evidence. The hearing officer shall rule on any such objections within seven
days of the filing of the objections.
c. The opening brief shall be filed by DMAS and the provider
within 30 days of the completion of the hearing.
d. Any reply brief from DMAS or the provider shall be filed
within 10 days of the filing of the opening brief to which the reply brief
responds.
2. If there has been an extension to the time for conducting
the hearing pursuant to subsection C of this section, the hearing officer is
authorized to alter the due dates for filing opening and reply briefs to permit
the hearing officer to be in compliance with the due date for the submission of
the recommended decision as required by § 32.1-325.1 B of the Code of Virginia
and subsection E of this section.
C. The hearing officer shall conduct the hearing within 45
days from the filing of the notice of formal appeal, unless the hearing
officer, DMAS, and the provider all mutually agree to extend the time for
conducting the hearing. Notwithstanding the foregoing, the due date for the
hearing officer to submit the recommended decision to the DMAS director, as
required by § 32.1-325.1 B of the Code of Virginia and subsection E of this
section, shall not be extended or otherwise changed.
D. Hearings shall be transcribed by a court reporter retained
by DMAS.
E. Upon completion of the hearing, DMAS and the provider
shall have 30 days to exchange and file with the hearing officer an opening
brief. Only opening briefs filed within 30 days after the hearing shall be
considered. DMAS and the provider shall have 10 days to exchange and file with
the hearing officer a reply brief after the opening brief has been filed. Only
reply briefs filed within 10 days after the opening brief has been filed shall
be considered.
F. E. The hearing officer shall submit a
recommended decision to the DMAS director with a copy to the provider within
120 days of receipt the filing of the formal appeal request
notice. If the hearing officer does not submit a recommended decision
within 120 days of the filing of the notice of formal appeal, then DMAS
shall give written notice to the hearing officer and the Executive Secretary of
the Supreme Court that a recommended decision is due.
G. F. Upon receipt of the hearing officer's
recommended decision, the DMAS director shall notify DMAS and the provider in
writing that any written exceptions to the hearing officer's recommended
decision shall be filed with the DMAS Appeals Division within 30 14
days of receipt of the DMAS director's letter. Only exceptions filed within 30
14 days of receipt of the DMAS director's letter shall be considered. The
DMAS director shall issue the final agency case decision within 60 days of
receipt of the hearing officer's recommended decision.
G. The DMAS director shall issue the final agency decision
within 60 days of receipt of the hearing officer's recommended decision in
accordance with § 32.1-325.1 B of the Code of Virginia.
VA.R. Doc. No. R14-3105; Filed June 21, 2016, 10:32 a.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Fast-Track Regulation
Title of Regulation: 12VAC30-30. Groups Covered and
Agencies Responsible for Eligibility Determination (adding 12VAC30-30-70).
Statutory Authority: § 32.1-325 of the Code of
Virginia; 42 USC § 1396 et seq.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: August 10, 2016.
Effective Date: August 26, 2016.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, Policy Division, 600 East Broad
Street, Suite 1300, Richmond, VA 23219, telephone (804) 371-4300, FAX (804)
786-1680, or email emily.mcclellan@dmas.virginia.gov.
Basis: Section 32.1-325 of the Code of Virginia grants
to the Board of Medical Assistance Services the authority to administer and
amend the Plan for Medical Assistance. Section 32.1-324 of the Code of Virginia
authorizes the Director of the Department of Medical Assistance Services (DMAS)
to administer and amend the Plan for Medical Assistance according to the
board's requirements. The Medicaid authority as established by § 1902(a) of the
Social Security Act (42 USC § 1396a) provides governing authority for
payments for services.
The new section, 12VAC30-30-70, is required by 42 CFR
435.1110, a federal regulation stating that DMAS "must provide Medicaid
during a presumptive eligibility period to individuals who are determined by a
qualified hospital, on the basis of preliminary information, to be
presumptively eligible [for Medicaid]". The federal regulation states that
the requirements of 42 CFR 435.1102 and 42 CFR 435.1103 apply to
these determinations.
Purpose: The purpose of this action is to comply with
federal regulations, which require DMAS to permit qualified hospitals to make
presumptive eligibility determinations.
The regulations protect the health, safety, and welfare of
citizens by promoting enrollment in Medicaid for individuals who may be
eligible but who are not enrolled. The changes allow these individuals to
receive Medicaid covered services during the presumptive eligibility period.
The changes assure individuals timely access to care while a final eligibility
determination is made and promote enrollment in Medicaid.
These changes assist both the individual with the cost of the
medical care they receive and assist the hospital, which can be assured of
payment for services rendered.
Rationale for Using Fast-Track Rulemaking Process: This
regulatory change is expected to be noncontroversial because the federal
government has required all states to make this change; it is nondiscretionary.
Further, the regulatory change is expected to be noncontroversial
because DMAS engaged stakeholder groups in making certain choices that are
permitted by the federal regulations. DMAS worked closely with the Virginia
Hospital and Healthcare Association on both the content of the changes and on
training materials for hospitals. As of August 2014, 57 hospitals across
Virginia are qualified to make presumptive eligibility determinations.
Substance: The section of the State Plan for Medical
Assistance affected by this action is Groups Covered and Agencies Responsible
for Eligibility Determination (12VAC30-30).
Federal regulations require DMAS to implement these regulatory
changes and to establish the requirements that hospitals must meet in order to
participate. (The hospital must be a Medicaid provider, must notify DMAS of its
election to make presumptive eligibility determinations, and must do so in
accordance with state policies and procedures. The hospital must not have been
disqualified for failing to follow these policies and procedures.) DMAS chose
to allow hospitals to use an abbreviated online form to determine presumptive
eligibility, rather than using the full Medicaid application for this purpose;
individuals are not required to sign this online form. DMAS also chose to
require hospitals to assist the individual with completing and submitting a
full Medicaid application.
The federal requirements also establish a minimum set of groups
that must be considered for possible presumptive eligibility, as follows: (i)
pregnant women; (ii) infants and children younger than age 19 years, parents,
and other caretaker relatives; (iii) adults if covered by the state; (iv)
individuals with an income above 133% of the federal poverty level and younger
than age 65 years if covered by the state; (v) individuals eligible for family
planning services if covered by the state; (vi) former foster care children;
and (vii) individuals needing treatment for breast or cervical cancer if
covered by the state. The eligibility determination for selected groups (i),
(ii), (v), (vi) and (vii) does not require that hospitals evaluate the
resources of these individuals. Thus, these hospital eligibility determinations
are more likely to be more accurate.
Virginia currently does not cover groups (iii) and (iv), thus
these two groups are not covered under hospital presumptive eligibility. DMAS
elected not to provide coverage to other nonmandated groups because the other
nonmandated groups require resource tests.
In accordance with federal requirements, presumptive
eligibility is determined based on membership in one of the above groups:
household income, state residency, and immigration status. State residency and
immigration status were options permitted by the Centers for Medicare and
Medicaid Services (CMS) and chosen by DMAS because this is consistent with the
rest of Virginia Medicaid eligibility. Federal regulations establish when the
presumptive eligibility period begins (the date the presumptive eligibility
determination is made) and ends, which is the earlier of the (i) day on which a
decision is made on a full Medicaid application; or (ii) last day of the month
following the month that the hospital presumptive eligibility determination was
made and no full Medicaid application was filed.
CMS required the Commonwealth to set performance standards for
hospitals performing presumptive eligibility determinations. Virginia opted to
set standards related to the percentage of individuals who submit a full
Medicaid application and who are subsequently determined to be eligible for
Medicaid as a result of that application. In Virginia, the standards are that
85% of individuals who are determined to be presumptively eligible by a
hospital must file a full application for Medicaid. Of those individuals, 70%
must be determined eligible for Medicaid based on their full application. If
hospitals fail to meet these standards after corrective action plans are put
into place, their authority to make presumptive eligibility determinations may
be terminated.
Issues: The primary advantages of this regulatory action
are that it will enable DMAS to comply with federal requirements; will promote
Medicaid enrollment among individuals who are eligible for Medicaid but not
enrolled; and will permit hospitals to receive Medicaid reimbursement for
covered services rendered.
With regard to hospital reimbursement, services covered during
a presumptive eligibility period will be considered Medicaid-covered services
for year-end hospital cost reporting purposes. For hospitals that receive
supplemental reimbursement for indigent care, the amount of indigent care
reimbursement will be reduced due to the increased Medicaid reimbursement.
There are no known disadvantages to the public, the department,
or the Commonwealth.
Department of Planning and Budget's Economic Impact Analysis:
Summary of the Proposed Amendments to Regulation. The proposed
regulations establish rules for federally required Medicaid presumptive
eligibility determinations made by hospitals for their patients seeking
treatment.
Result of Analysis. The benefits likely exceed the costs for
all proposed changes. An alternative or an additional standard may improve the
regulation in measuring a hospital's performance. Additional regulatory
language about the length of the disqualification period may improve the
regulation. Additional language may be needed to dissuade applicants from being
untruthful.
Estimated Economic Impact. Starting in January 2014, the
federal Affordable Care Act provided qualified hospitals an opportunity to make
Medicaid presumptive eligibility determinations for their patients seeking
treatment. States must allow all qualifying hospitals willing to abide by state
policies and procedures to perform presumptive eligibility determinations.
Federal regulations in 42 CFR 435.1101 and 42 CFR 435.1102 outline the
details regarding the implementation of this requirement by the states.
Virginia's presumptive eligibility rules were approved by the Centers for
Medicare and Medicaid Services (CMS) in July 2015 and have already been
implemented under the approved state plan. In fiscal year 2015, approximately
$3.5 million in total expenditures was paid for 19,423 claims involving 2,079
unique recipients.
Under the presumptive eligibility rules, Medicaid eligibility
determinations are made by trained hospital staff based on an assessment of the
individual's status as a member of a group (i.e., pregnant women, infants and
children under age 19, parents and other caretaker relatives, individuals
eligible for family planning services, former foster care children, individuals
needing treatment for breast and cervical cancer), their income, state
residency, and citizenship status. The hospital then assists the individual in
completing and submitting a full Medicaid application for future Medicaid
coverage. If the individual is found presumptively eligible, he or she is
temporarily enrolled in Medicaid and health care providers receive payment for
services provided during this interim period. A full application for Medicaid
coverage may follow, with the determination of eligibility completed by a local
department of social services, or the Department of Medical Assistance Services
(DMAS). The presumptive eligibility begins on the date the determination is
made and ends on the earlier of the day on which a decision is made on a full
Medicaid application, or the last day of the month following the month that the
hospital's presumptive eligibility determination was made and no full Medicaid
application was filed. Payment for services covered is guaranteed during the
presumptive eligibility period. There is no recoupment for Medicaid services
provided during that period resulting from erroneous determinations made by
qualified entities.
Pursuant to a request by CMS, the proposed regulation establishes
two performance standards for hospitals performing presumptive eligibility
determinations. In order to maintain their participation to make presumptive
eligibility determinations, a hospital is required to ensure (i) that a certain
percentage of individuals deemed presumptively eligible will file a full
Medicaid application before the end of the presumptive eligibility period, and
(ii) that a certain percentage of individuals deemed presumptively eligible
will be determined eligible based on the full application. The purpose of the
proposed performance standards is to ensure that hospitals are making
appropriate presumptive eligibility determinations and fulfilling their
oversight responsibilities. If a hospital fails to follow these standards it may
be disqualified from making such determinations.
DMAS recognizes if not carefully implemented, the proposed
performance standards for participating hospitals could have unintended adverse
effects on their ability to participate in the program through no fault of
their own.
A performance standard must be under the control of the entity
whose performance it measures. In this case, a hospital does not have control
over whether the individuals deemed presumptively eligible will file a full
Medicaid application. The individual may not want to file a full Medicaid
application or may even refuse to do so. The individual's failure to follow
through with the full application should not be held against the performance of
a qualified hospital and put its participation in jeopardy. In order to avoid
such unintended consequences, such cases will be excluded in calculating the
performance metric when the hospital certifies that an attempt has been made
but the individual declined to follow through with the full application.
Similarly, the hospital does not have control over whether the
individual is providing accurate or even truthful information when filing the
application for the presumptive eligibility. Additionally, comparison of
determinations made at two different points in time may lead to erroneous
conclusions as the applicant's financial circumstances may have changed between
the interim and the full applications. Thus, a participating hospital will not
be held liable if the information provided by the applicant results in a denial
of eligibility following the full application; such cases will also be excluded
from the data in calculating the performance metric. In the alternative, this
performance standard may perhaps focus solely on whether the hospital made an error
in its presumptive eligibility determination treating the information on the
application as true.
DMAS notes that these two performance measures were suggested
by CMS and any revision in these measures would necessitate a state plan
amendment. It appears that the states have the option to choose different
performance standards than those suggested by CMS.1
The primary advantages of this regulatory action are that it
enables DMAS to comply with federal requirements, assures individuals timely
but limited access to care, promotes Medicaid enrollment among individuals who
are eligible for Medicaid but not enrolled, and permits hospitals to receive
Medicaid reimbursement for covered services rendered. Since the presumptive
eligibility program has already been implemented since July 2015, no
significant economic impact is expected upon promulgation of the proposed
changes other than providing the rules in the regulations for the affected
entities and the public.
The proposed regulation may be improved by addressing the
length of the disqualification period and when and how a reinstatement could
occur if a hospital fails to meet the performance standards. It does not make
sense to prohibit a hospital from participation in this program indefinitely.
Further, as discussed above, there is no recoupment for
payments from hospitals for services provided during the presumptive
eligibility period. Without such a guarantee, a hospital could not rely on the
presumptive eligibility determination and may be inclined to refrain from
participation. However, given the unique nature of this program, the applicant
should be held liable when he or she intentionally provides false information.
The proposed regulation may be further improved by making it clear that the
applicant may be held liable or by requiring disclosure of such a potential
liability on the application form. Such language would dissuade applicants from
being untruthful and mitigate the Commonwealth's exposure to risk of fraud.
Businesses and Entities Affected. The proposed regulation
primarily applies to hospitals wishing to participate in presumptive
eligibility determinations and the individuals who may presumptively qualify
for Medicaid. As of August 2014, there were 57 hospitals making presumptive
eligibility determinations. In fiscal year 2015, there were 2,079 recipients
identified as presumptively eligible.
Localities Particularly Affected. The proposed changes apply
statewide.
Projected Impact on Employment. A hospital may voluntarily
choose to participate in presumptive eligibility determinations. Such
participation may increase their demand for labor to assist the individuals in
the application process.
Effects on the Use and Value of Private Property. Participation
in presumptive eligibility determinations helps hospitals receive payment from
Medicaid for eligible individuals. In that sense, the proposed regulation has a
positive impact on the asset values of participating hospitals.
Real Estate Development Costs. No impact on real estate
development costs is expected.
Small Businesses:
Definition. Pursuant to § 2.2-4007.04 of the Code of Virginia,
small business is defined as "a business entity, including its affiliates,
that (i) is independently owned and operated and (ii) employs fewer than 500
full-time employees or has gross annual sales of less than $6 million."
Costs and Other Effects. Affected hospitals are not considered
small businesses.
Alternative Method that Minimizes Adverse Impact. The proposed
changes do not affect small businesses.
Adverse Impacts:
Businesses. The proposed changes are not anticipated to have an
adverse impact on businesses.
Localities. The proposed amendments should not adversely affect
localities.
Other Entities. The proposed changes are not anticipated to
have an adverse impact on other entities.
_________________
Agency's Response to Economic Impact Analysis: The agency
has reviewed the economic impact analysis prepared by the Department of
Planning and Budget. The agency raises no issues with this analysis.
Summary:
This action creates a new section, 12VAC30-30-70, Hospital
presumptive eligibility, in accordance with federal regulations that require
the Department of Medical Assistance Services to allow qualified hospitals to
make temporary Medicaid eligibility determinations for individuals who are
seeking medical treatment. The Medicaid determinations are made by trained
hospital staff based on an assessment of an individual's status as a member of
an eligible group and an individual's income, state residency, and citizenship
status. The hospital then assists the individual in completing and submitting a
full Medicaid application for future Medicaid coverage.
12VAC30-30-70. Hospital presumptive eligibility.
A. Qualified hospitals shall administer presumptive
eligibility in accordance with the provisions of this section. A qualified
hospital is a hospital that:
1. Has entered into a valid provider agreement with DMAS,
participates as a Virginia Medicaid provider, notifies DMAS of its election to
make presumptive eligibility determinations, and agrees to make presumptive
eligibility determinations consistent with DMAS policies and procedures; and
2. Has not been disqualified by DMAS for failure to make
presumptive eligibility determinations in accordance with applicable state
policies and procedures or for failure to meet any standards established by the
Medicaid agency.
B. The eligibility groups or populations for which
hospitals determine eligibility presumptively are: (i) pregnant women; (ii)
infants and children younger than age 19 years; (iii) parents and other
caretaker relatives; (iv) individuals eligible for family planning services;
(v) former foster care children; and (vi) individuals needing treatment for
breast and cervical cancer.
C. The presumptive eligibility determination shall be
based on:
1. The individual's categorical or nonfinancial eligibility
for the group, as listed in subsection B of this section, for which the
individual's presumptive eligibility is being determined;
2. Household income shall not exceed the applicable income
standard for the group, as the groups are listed in subsection B of this
section, for which the individual's presumptive eligibility is being determined
if an income standard is applicable for this group;
3. Virginia residency; and
4. Satisfactory immigration status.
D. Qualified hospitals shall ensure that at least 85% of individuals
deemed by the hospital to be presumptively eligible will file a full Medicaid
application before the end of the presumptive eligibility period.
E. Qualified hospitals shall ensure that at least 70% of
individuals deemed by the hospital to be presumptively eligible are determined
eligible for Medicaid based on the full application that is submitted before
the end of the presumptive eligibility period.
F. The presumptive eligibility period shall begin on the
date the presumptive eligibility determination is made. The presumptive
eligibility period shall end on the earlier of:
1. The date the eligibility determination for regular
Medicaid is made if an application for Medicaid is filed by the last day of the
month following the month in which the determination of presumptive eligibility
is made; or
2. The last day of the month following the month in which
the determination of presumptive eligibility is made if no application for
Medicaid is filed by last day of the month following the month in which the
determination of presumptive eligibility is made.
G. Periods of presumptive eligibility are limited to one
presumptive eligibility period per pregnancy and one per calendar year for all
other covered groups.
VA.R. Doc. No. R16-4431; Filed June 21, 2016, 10:07 a.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Emergency Regulation
Title of Regulation: 12VAC30-60. Standards
Established and Methods Used to Assure High Quality Care (amending 12VAC30-60-303, 12VAC30-60-310;
adding 12VAC30-60-301, 12VAC30-60-302, 12VAC30-60-304, 12VAC30-60-305,
12VAC30-60-306, 12VAC30-60-308, 12VAC30-60-313, 12VAC30-60-315; repealing
12VAC30-60-300, 12VAC30-60-307, 12VAC30-60-312).
Statutory Authority: § 32.1-325 of the Code of
Virginia; 42 USC § 1396 et seq.
Effective Dates: September 1, 2016, through February 28,
2018.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, Policy Division, 600 East Broad
Street, Suite 1300, Richmond, VA 23219, telephone (804) 371-4300, FAX (804)
786-1680, or email emily.mcclellan@dmas.virginia.gov.
Preamble:
Section 2.2-4011 B of the Code of Virginia authorizes state
agencies to adopt emergency regulations in situations in which Virginia
statutory law or the appropriation act or federal law or federal regulation
requires that a regulation become effective in 280 days or less from its
enactment, and the regulation is not exempt under the provisions of
§ 2.2-4006 A 4. Chapter 413 of the 2014 Acts of Assembly, Item 301 QQQQ of
Chapter 3 of the 2015 Acts of the Assembly, and Item 306 PPP of Chapter 780 of
the 2016 Acts of Assembly direct the Department of Medical Assistance Services
(DMAS) to contract out community-based screenings for children, track and
monitor all requests for screenings that have not been completed within 30 days
of an individual's request, establish reimbursement and tracking mechanisms,
and promulgate regulations to implement these provisions to be effective within
280 days of enactment. This emergency regulatory action responds to the
legislative mandates.
In 1984, the Code of Virginia was modified to add
§ 32.1-330, Preadmission screening required. Section 32.1-330 of the Code
of Virginia requires that all individuals who will be eligible for community or
institutional long-term services and supports (LTSS) as defined in the State
Plan for Medical Assistance be evaluated to determine their needs for
Medicaid-funded nursing facility services. Also, the Code of Virginia
specifically requires DMAS to utilize employees of local departments of social
services and local health departments for community screenings and acute care
hospitals for inpatient screenings, respectively. While this screening
structure, established in the early 1980s, worked effectively for many years,
the evolution of Virginia's Medicaid service delivery system has outgrown the
original design. Significant challenges have developed that require a change to
the Virginia Administrative Code. Some community-based screenings have taken
longer than 30 days to complete thereby creating a significant risk to
individuals who have been unable to access Medicaid LTSS.
The existing regulations for nursing facility criteria and
preadmission screening were first promulgated in 1994 and amended in 2002. The
regulations include the criteria for receiving Medicaid-funded community-based
and nursing facility long-term services and supports. This emergency regulation
adds requirements for accepting, managing, and completing requests for
community and hospital electronic screenings for community-based and nursing
facility services, and using the electronic preadmission screening (ePAS)
system.
One potential issue may be limited staff resources in
community and hospital settings. The emergency regulation clarifies
requirements of community and hospital preadmission teams and includes
requirements to use the new automated ePAS system to enhance work efficiency.
This emergency regulation also establishes the use by DMAS of a contractor or
contractors and provides a framework for public or private entities to screen
children and adults in communities where community preadmission screening teams
are unable to complete screenings within 30 days of the initial request date for
a screening. These strategies are designed to ensure prompt services to
citizens requesting Medicaid-funded LTSS and to protect their health, safety,
and welfare.
The current requirements for functional eligibility
(12VAC30-60-303 B) for Medicaid-funded LTSS are being retained since these
standards support the eligibility process for the DMAS home-based and
community-based waiver programs (the Elderly or Disabled with Consumer
Direction Waiver, the Technology Assisted Waiver, the Alzheimer's Assisted Living
Waiver, the Program of All-Inclusive Care for the Elderly Program, and nursing
facility care).
The regulations repeal the existing nursing facility
criteria (12VAC30-60-300) in order to move the criteria to a new location
within 12VAC30-60-303. To be clear, the functional criteria, based on the
Uniform Assessment Instrument (UAI) form, are not changing in this regulatory
action, and the use of the UAI for this purpose remains the same. This action
simply moves the existing criteria to a new location in the chapter to assist
the public and regulated entities to more easily understand the regulation.
The remaining current provisions in the Virginia
Administrative Code are incomplete and fragmented. To remedy this, amendments
include adding a definitions section (12VAC30-60-301) and sections describing
the requirement for the request for screenings (12VAC30-60-304), screenings for
Medicaid-funded LTSS (12VAC30-60-305), submission of screenings (12VAC30-306),
ePAS requirements and submissions (12VAC30-60-310), individuals determined to
not meet criteria (12VAC30-60-313), and ongoing evaluations for individuals
receiving Medicaid-funded LTSS (12VAC30-60-315).
12VAC30-60-300. Nursing facility criteria. (Repealed.)
A. Medicaid-funded long-term care services may be provided
in either a nursing facility or community-based care setting. The criteria for
assessing an individual's eligibility for Medicaid payment of nursing facility
care consist of two components: (i) functional capacity (the degree of
assistance an individual requires to complete activities of daily living) and
(ii) medical or nursing needs. The criteria for assessing an individual's
eligibility for Medicaid payment of community-based care consist of three
components: (i) functional capacity (the degree of assistance an individual
requires to complete activities of daily living), (ii) medical or nursing needs
and (iii) the individual's risk of nursing facility placement in the absence of
community-based waiver services. In order to qualify for either Medicaid-funded
nursing facility care or Medicaid-funded community-based care, the individual
must meet the same criteria.
B. The preadmission screening process preauthorizes a
continuum of long-term care services available to an individual under the Virginia
Medical Assistance Program. Nursing Facilities' Preadmission Screenings to
authorize Medicaid-funded long-term care are performed by teams composed by
agencies contracting with the Department of Medical Assistance Services (DMAS).
The authorization for Medicaid-funded long-term care must be rescinded by the
nursing facility or community-based care provider or by DMAS at any point that
the individual is determined to no longer meet the criteria for Medicaid-funded
long-term care. Medicaid-funded long-term care services are covered by the
program for individuals whose needs meet the criteria established by program
regulations. Authorization of appropriate non-institutional services shall be
evaluated before nursing facility placement is considered.
C. Prior to an individual's admission, the nursing
facility must review the completed pre-admission screening forms to ensure that
appropriate nursing facility admission criteria have been documented. The
nursing facility is also responsible for documenting, upon admission and on an
ongoing basis, that the individual meets and continues to meet nursing facility
criteria. For this purpose, the nursing facility will use the Minimum Data Set
(MDS) The post admission assessment must be conducted no later than 14 days
after the date of admission and promptly after a significant change in the
resident's physical or mental condition. If at any time during the course of
the resident's stay, it is determined that the resident does not meet nursing
facility criteria as defined in the State Plan for Medical Assistance, the
nursing facility must initiate discharge of such resident. Nursing facilities
must conduct a comprehensive, accurate, standardized, reproducible assessment
of each resident's functional capacity and medical and nursing needs.
The Department of Medical Assistance Services shall
conduct surveys of the assessments completed by nursing facilities to determine
that services provided to the residents meet nursing facility criteria and that
needed services are provided.
D. The community-based provider is responsible for
documenting upon admission and on an ongoing basis that the individual meets
the criteria for Medicaid-funded long-term care.
E. The criteria for nursing facility care under the
Virginia Medical Assistance Program are contained herein. An individual's need
for care must meet these criteria before any authorization for payment by
Medicaid will be made for either institutional or non-institutional long-term
care services. The Nursing Home Pre-Admission Screening team is responsible for
documenting on the state-designated assessment instrument that the individual
meets the criteria for nursing facility or community-based waiver services and
for authorizing admission to Medicaid-funded long-term care. The rating of
functional dependencies on the assessment instrument must be based on the
individual's ability to function in a community environment, not including any
institutionally induced dependence.
12VAC30-60-301. Definitions.
The following words and terms as used in 12VAC30-60-302
through 12VAC30-60-315 shall have the following meanings unless the context
clearly indicates otherwise:
"Activities of daily living" or "ADLs"
means personal care tasks such as bathing, dressing, toileting, transferring,
and eating/feeding. An individual's degree of independence in performing these
activities is a part of determining appropriate level of care and service
needs.
"Adult" means a person age 18 years or older who
may need Medicaid-funded long-term services and supports (LTSS) or who becomes
eligible to receive Medicaid-funded LTSS.
"Appeal" means the processes used to challenge
actions regarding services, benefits, and reimbursement provided by Medicaid
pursuant to 12VAC30-110 and Part XII (12VAC30-20-500 et seq.) of 12VAC30-20.
"At risk" means the need for the level of care
provided in a hospital, nursing facility, or an Intermediate Care Facility for
Individuals with Intellectual Disability (ICF/IID) when there is reasonable
indication that the individual is expected to need the services in the near
future (that is, one month or less) in the absence of home or community-based
services.
"Child" means a person up to the age of 18 years
who may need Medicaid-funded LTSS or who becomes eligible to receive
Medicaid-funded LTSS.
"Choice" means the individual is provided the
option of either home and community-based services or institutional services
and supports, including the Program of All-Inclusive Care for the Elderly
(PACE), if available and appropriate, after the individual has been determined
likely to need LTSS.
"Communication" means all forms of sharing
information and includes oral speech and augmented or alternative communication
used to express thoughts, needs, wants, and ideas, such as the use of a
communication device, interpreter, gestures, and picture/symbol communication
boards.
"Community-based screening" means the
face-to-face process conducted pursuant to § 32.1-330 of the Code of Virginia
to determine whether an individual meets the criteria for Medicaid-funded LTSS
and that shall be conducted in the individual's place of residence or, at the
request of the individual, an alternate location within the same jurisdiction.
"Community-based services" or "CBS"
means community-based services waivers or the Program of All-Inclusive Care for
the Elderly (PACE).
"Community-based services provider" or "CBS
provider" means a provider or agency enrolled with Virginia Medicaid to
offer services to individuals eligible for home and community-based waivers
services or PACE.
"Community-based team" or "CBT" means
a nurse, social worker, or other assessors designated by the department and a
physician who are employees of, or contracted with, the Virginia Department of
Health or the local department of social services.
"DARS" means the Virginia Department for Aging
and Rehabilitative Services.
"Day" means calendar day unless specified
otherwise.
"DBHDS" means the Virginia Department of
Behavioral Health and Developmental Services.
"DMAS" or "the department" means the
Department of Medical Assistance Services.
"DMAS designee" means the public or private
entity with an agreement with the Department of Medical Assistance Services to
complete preadmission screenings pursuant to § 32.1-330 of the Code of
Virginia.
"Electronic preadmission screening" or
"ePAS" means the automated system for use by all entities contracted
by DMAS to perform preadmission screenings pursuant to § 32.1-330 of the Code
of Virginia.
"Face-to-face" means an in-person meeting with
the individual seeking Medicaid-funded LTSS that may also occur through
technological means that permit visualization and real-time communication with
the individual if circumstances prohibit in-person access to the individual.
"Feasible alternative" means a range of services
that can be provided in the community, for less than the cost of comparable
institutional care, in order to enable an individual to continue living in the
community.
"Home and community-based services waiver" or
"waiver services" means the range of community services and supports
approved by the Centers for Medicare and Medicaid Services (CMS) pursuant to §
1915(c) of the Social Security Act to be offered to individuals as an
alternative to institutionalization.
"Hospital team" means persons designated by the
hospital who are responsible for conducting and submitting the PAS for
inpatients to the DMAS automated system.
"Inpatient" means an individual who has a
physician's order for admission to an acute care hospital, rehabilitation
hospital, or a rehabilitation unit in an acute care hospital.
"Institutional screening" means the face-to-face
process conducted pursuant to § 32.1-330 of the Code of Virginia for
individuals who are inpatients in hospitals to determine whether an individual
meets the criteria for Medicaid-funded LTSS.
"Licensed health care professional" or
"LHCP" means a registered nurse, nurse practitioner, or physician
currently employed or contracted by the Virginia Department of Health and
licensed by the relevant health regulatory board of the Department of Health
Professions who is practicing within the scope of his license.
"Local department of social services" or
"LDSS" means the entity established under § 63.2-324 of the Code of
Virginia by the governing city or county in the Commonwealth.
"Local health department" or "LHD"
means the entity established under § 32.1-31 of the Code of Virginia.
"Long-term services and supports" or
"LTSS" means a variety of services that help individuals with health
or personal care needs and ADLs over a period of time that can be provided in
the home, the community, assisted living facilities, or nursing facilities.
"Medicaid" means the program set out in the 42
USC § 1396 and administered by the Department of Medical Assistance Services
consistent with Chapter 10 (§ 32.1-323 et seq.) of Title 32.1 of the Code of
Virginia.
"Medicare" means the Health Insurance for the
Aged and Disabled program as administered by the Centers for Medicare and
Medicaid Services pursuant to 42 USC 1395ggg.
"Nursing facility" or "NF" means any
nursing home as defined in § 32.1-123 of the Code of Virginia.
"Other assessor designated by DMAS" means an
employee of the local department of social services holding the occupational
title of family services specialist.
"Preadmission screening," "PAS," or
"screening" means the process to (i) evaluate the functional,
nursing, and social support needs of individuals referred for preadmission
screening for certain long-term care services requiring NF eligibility; (ii) assist
individuals in determining what specific services the individual needs; (iii)
evaluate whether a service or a combination of existing community services are
available to meet the individual's needs; and (iv) provide a list to
individuals of appropriate providers for Medicaid-funded nursing facility or
home and community-based services for those individuals who meet nursing
facility level of care.
"Program of All-Inclusive Care for the Elderly"
or "PACE" means the community-based service pursuant to § 32.1-330.3
of the Code of Virginia.
"Referral for screening" means information
obtained from an interested person or other third party having knowledge of an
individual who may need Medicaid-funded LTSS and may include, for example, a
physician, PACE provider, service provider, family member, or neighbor who is
able to provide sufficient information to enable contact with the individual.
"Reimbursement" means the evaluation of the
submitted claims for completeness, accuracy, and service resulting in the
payment by DMAS for the services represented on the claims.
"Representative" means a person who is
authorized to make decisions on behalf of the individual.
"Request date for screening" or "request
date" means the date (i) that an individual or the individual's
representative contacts the screening entity in the jurisdiction where the
individual resides asking for assistance with LTSS or, (ii) for hospital
inpatients, that a physician orders case management consultation or case
management determines the need for LTSS upon discharge from a hospital.
"Request for screening" means (i) communication
from an individual, individual's representative, adult protective services
(APS), or child protective services (CPS) expressing the need for LTSS, or (ii)
for hospital inpatients, a physician order for case management consultation or
case management determination of the need for LTSS upon discharge from a
hospital.
"Residence" means an individual's private home,
apartment, assisted living facility, nursing facility, or jail/correctional facility,
for example, if the individual to be screened is seeking Medicaid-funded LTSS
and does not request an alternative screening location as allowed in
12VAC30-60-305 A.
"Screening entity" means the hospital screening
team, community-based team (CBT), or DMAS designee contracted to perform
preadmission screenings pursuant to § 32.1-330 of the Code of Virginia.
"Significant change in circumstances" means a
change in an individual's condition that is expected to last longer than 30
days and shall not include short-term changes that resolve with or without
intervention; a short-term illness or episodic event; or a well-established,
predictive, cyclic pattern of clinical signs and symptoms associated with a
previously diagnosed condition where an appropriate course of treatment is in
progress.
"Submission" means the transmission of the
screening findings and receipt of successfully processed results using the DMAS
automated system.
"Submission date" means the date that the
screening entity transmits to DMAS the screening findings using the DMAS
automated system.
"Uniform Assessment Instrument" or
"UAI" means the standardized multidimensional assessment instrument
that is completed by the screening entity that assesses an individual's
physical health, mental health, and psycho/social and functional abilities to
determine if the individual meets the nursing facility level of care.
"VDH" means the Virginia Department of Health.
"VDSS" means the Virginia Department of Social
Services.
12VAC30-60-302. Introduction; access to Medicaid-funded
long-term services and supports.
A. Medicaid-funded long-term services and supports (LTSS)
may be provided in either community-based or institutional-based settings. To
receive LTSS, the individual's condition shall first be evaluated using the
designated assessment instrument, the Uniform Assessment Instrument (UAI), and
other designated forms. Screening entities shall use the DMAS-designated forms
(UAI, DMAS-95, DMAS-96, DMAS-95 Level I (MI/IDD/RC) and if appropriate, DMAS-95
Level II (for nursing facility placements only), and the DMAS-97) to perform
preadmission screenings for LTSS.
1. An individual's need for LTSS shall meet the established
criteria (12VAC30-60-303) before any authorization for reimbursement by
Medicaid is made for LTSS.
2. Appropriate community-based services shall be evaluated
prior to consideration of nursing facility placement.
B. The evaluation shall be the preadmission screening
(PAS) or screening process, as designated in § 32.1-330 of the Code of
Virginia, which shall preauthorize a continuum of LTSS covered by Medicaid.
1. Such screenings, using the UAI, shall be conducted by
teams of representatives of (i) hospitals for individuals (adults and children)
who are inpatients; (ii) local departments of social services and local health
departments, known herein as CBTs, for individuals (adults) residing in the
community and who are not inpatients; or (iii) a DMAS designee for individuals
(children) residing in the community who are not inpatients. All of these
entities shall be contracted with DMAS to perform this activity and be
reimbursed by DMAS.
2. All screenings shall be comprehensive, accurate,
standardized, and reproducible evaluations of individual functional capacities,
medical or nursing needs, and risk for institutional placement.
C. The authorization for Medicaid-funded LTSS shall be
rescinded by the community-based services provider, the NF, or DMAS when the
individual is determined to no longer meet the criteria for Medicaid-funded
LTSS. The individual shall have the right to appeal such rescission decision.
The individual shall be responsible for all expenditures made after the date of
the rescission decision in the event that the rescission is upheld on appeal.
D. Individuals shall not be required to be financially
eligible for receipt of Medicaid or have submitted an application for Medicaid
in order to be screened for LTSS.
E. Pursuant to § 32.1-330 of the Code of Virginia,
individuals shall be screened if they are eligible for Medicaid or are
anticipated to become eligible for Medicaid reimbursement of their NF care
within six months of nursing facility placement.
12VAC30-60-303. Preadmission screening criteria for Medicaid-funded
long-term care services and supports.
A. Functional dependency alone is shall not be
deemed sufficient to demonstrate the need for nursing facility care or
placement or authorization for community-based care services. An
individual shall be determined to meet the nursing facility criteria when:
1. The individual has both limited functional capacity and
medical or nursing needs according to the requirements of this section; or
2. The individual is rated dependent in some functional
limitations, but does not meet the functional capacity requirements, and the
individual requires the daily direct services or supervision of a licensed
nurse that cannot be managed on an outpatient basis (e.g., clinic, physician
visits, home health services).
B. An individual shall only be considered to meet the
nursing facility criteria when both the functional capacity of the individual
and his medical or nursing needs meet the following requirements. Even when an
individual meets nursing facility criteria, placement in a noninstitutional
setting shall be evaluated before actual nursing facility placement is
considered In order to qualify for Medicaid-funded LTSS, the individual
shall meet the following criteria:
1. For Medicaid-funded nursing facility services to be
authorized, the screening entity shall document that the individual has both
functional and medical or nursing needs. The criteria for screening an
individual's eligibility for Medicaid reimbursement of NF services shall
consist of two components: (i) functional capacity (the degree of assistance an
individual requires to complete ADLs) and (ii) medical or nursing needs. The
rating of functional dependency on the UAI shall be based on the individual's
ability to function in a community environment and exclude all institutionally
induced dependencies.
2. For Medicaid-funded community-based services to be
authorized, an individual shall not be required to be physically admitted to a
NF. The criteria for screening an individual's eligibility for Medicaid reimbursement
of community-based services shall consist of three components: (i) functional
capacity needs (the degree of assistance an individual requires in order to
complete ADLs), (ii) medical or nursing needs, and (iii) the individual's risk
of NF placement within 30 days in the absence of community-based services.
1. C. Functional capacity.
a. 1. When documented on a completed
state-designated preadmission screening assessment instrument a UAI
that is completed in a manner consistent with the definitions of activities of
daily living (ADLs) and directions provided by DMAS for the rating of
those activities, individuals may be considered to meet the functional capacity
requirements for nursing facility care when one of the following describes
their functional capacity:
(1) a. Rated dependent in two to four of the Activities
of Daily Living ADLs, and also rated semi-dependent or dependent in
Behavior Pattern and Orientation, and semi-dependent in Joint Motion or
dependent in Medication Administration.
(2) b. Rated dependent in five to seven of the Activities
of Daily Living ADLs, and also rated dependent in Mobility.
(3) c. Rated semi-dependent in two to seven of
the Activities of Daily Living ADLs, and also rated dependent in
Mobility and Behavior Pattern and Orientation.
b. 2. The rating of functional dependencies on
the preadmission screening assessment instrument must shall
be based on the individual's ability to function in a community environment,
not including any institutionally induced dependence. The following
abbreviations shall mean: I = independent; d = semi-dependent; D = dependent;
MH = mechanical help; HH = human help.
(1) a. Bathing.
(a) (1) Without help (I)
(b) (2) MH only (d)
(c) (3) HH only (D)
(d) (4) MH and HH (D)
(e) (5) Performed by Others (D)
(2) b. Dressing.
(a) (1) Without help (I)
(b) (2) MH only (d)
(c) (3) HH only (D)
(d) (4) MH and HH (D)
(e) (5) Performed by Others (D)
(f) (6) Is not Performed (D)
(3) c. Toileting.
(a) (1) Without help day or night (I)
(b) (2) MH only (d)
(c) (3) HH only (D)
(d) (4) MH and HH (D)
(e) (5) Performed by Others (D)
(4) d. Transferring.
(a) (1) Without help (I)
(b) (2) MH only (d)
(c) (3) HH only (D)
(d) (4) MH and HH (D)
(e) (5) Performed by Others (D)
(f) (6) Is not Performed (D)
(5) e. Bowel Function function.
(a) (1) Continent (I)
(b) (2) Incontinent less than weekly (d)
(c) (3) External/Indwelling Device/Ostomy --
self care (d)
(d) (4) Incontinent weekly or more (D)
(e) (5) Ostomy -- not self care (D)
(6) f. Bladder Function function.
(a) (1) Continent (I)
(b) (2) Incontinent less than weekly (d)
(c) (3) External device/Indwelling
Catheter/Ostomy -- self care (d)
(d) (4) Incontinent weekly or more (D)
(e) (5) External device -- not self care (D)
(f) (6) Indwelling catheter -- not self care (D)
(g) (7) Ostomy -- not self care (D)
(7) g. Eating/Feeding.
(a) (1) Without help (I)
(b) (2) MH only (d)
(c) (3) HH only (D)
(d) (4) MH and HH (D)
(e) (5) Spoon fed (D)
(f) (6) Syringe or tube fed (D)
(g) (7) Fed by IV or clysis (D)
(8) h. Behavior Pattern pattern
and Orientation orientation.
(a) (1) Appropriate or Wandering/Passive less
than weekly + Oriented (I)
(b) (2) Appropriate or Wandering/Passive less
than weekly + Disoriented -- Some Spheres (I)
(c) (3) Wandering/Passive Weekly/or more +
Oriented (I)
(d) (4) Appropriate or Wandering/Passive less
than weekly + Disoriented -- All Spheres (d)
(e) (5) Wandering/Passive Weekly/Some or more +
Disoriented -- All Spheres (d)
(f) (6) Abusive/Aggressive/Disruptive less than
weekly + Oriented or Disoriented (d)
(g) (7) Abusive/Aggressive/Disruptive weekly or
more + Oriented (d)
(h) (8) Abusive/Aggressive/Disruptive +
Disoriented -- All Spheres (D)
(9) i. Mobility.
(a) (1) Goes outside without help (I)
(b) (2) Goes outside MH only (d)
(c) (3) Goes outside HH only (D)
(d) (4) Goes outside MH and HH (D)
(e) (5) Confined -- moves about (D)
(f) (6) Confined -- does not move about (D)
(10) j. Medication Administration administration.
(a) (1) No medications (I)
(b) (2) Self administered -- monitored less than
weekly (I)
(c) (3) By lay persons, Administered/Monitored
(D)
(d) (4) By Licensed/Professional nurse
Administered/Monitored (D)
(11) k. Joint Motion motion.
(a) (1) Within normal limits or instability
corrected (I)
(b) (2) Limited motion (d)
(c) (3) Instability -- uncorrected or immobile
(D)
c. D. Medical or nursing needs. An individual
with medical or nursing needs is an individual whose health needs require
medical or nursing supervision or care above the level that could be provided
through assistance with Activities of Daily Living ADLs, Medication
Administration medication administration, and general supervision
and is not primarily for the care and treatment of mental diseases. Medical or
nursing supervision or care beyond this level is required when any one of the
following describes the individual's need for medical or nursing supervision:
(1) 1. The individual's medical condition
requires observation and assessment to assure evaluation of the person's need
for modification of treatment or additional medical procedures to prevent
destabilization, and the person has demonstrated an inability to self observe
or evaluate the need to contact skilled medical professionals;
(2) 2. Due to the complexity created by the
person's multiple, interrelated medical conditions, the potential for the
individual's medical instability is high or medical instability exists; or
(3) 3. The individual requires at least one
ongoing medical or nursing service. The following is a nonexclusive list of
medical or nursing services that may, but need not necessarily, indicate a need
for medical or nursing supervision or care:
(a) a. Application of aseptic dressings;
(b) b. Routine catheter care;
(c) c. Respiratory therapy;
(d) d. Supervision for adequate nutrition and
hydration for individuals who show clinical evidence of malnourishment or
dehydration or have recent history of weight loss or inadequate hydration that,
if not supervised, would be expected to result in malnourishment or
dehydration;
(e) e. Therapeutic exercise and positioning;
(f) f. Routine care of colostomy or ileostomy or
management of neurogenic bowel and bladder;
(g) g. Use of physical (e.g., side rails,
poseys, locked wards) and/or or chemical restraints, or both;
(h) h. Routine skin care to prevent pressure
ulcers for individuals who are immobile;
(i) i. Care of small uncomplicated pressure
ulcers and local skin rashes;
(j) j. Management of those with sensory,
metabolic, or circulatory impairment with demonstrated clinical evidence of
medical instability;
(k) k. Chemotherapy;
(l) l. Radiation;
(m) m. Dialysis;
(n) n. Suctioning;
(o) o. Tracheostomy care;
(p) p. Infusion therapy; or
(q) q. Oxygen.
d. Even when an individual meets nursing facility criteria,
provision of services in a noninstitutional setting shall be considered before
nursing facility placement is sought.
C. E. When assessing an individual 21 years
of age or younger screening a child, the teams who are screening
entity who is conducting preadmission screenings for long-term care
services LTSS shall utilize the electronic Uniform Assessment
Instrument (UAI) interpretive guidance as contained referenced
in DMAS' Medicaid Memo dated October 3, 2012, entitled "Development of
Special Criteria for the Purposes of Pre-Admission Screening," which can
be accessed on the DMAS website at https://www.virginiamedicaid.dmas.virginia.gov/.
12VAC30-60-304. Requests for screening for adults and
children living in the community and adults and children in hospitals.
A. Screenings for adults living in the community.
Screenings for adults who are residing in the community but who are not
inpatients in acute care hospitals shall be completed and submitted to the DMAS
automated system within 30 days of the request date for screening.
1. Requests for screenings shall be accepted from either an
individual, the individual's representative, or an adult protective services
worker having an interest in the individual. The community-based team (CBT) in
the jurisdiction where the individual resides shall conduct such screening. For
the screening to be scheduled by the CBT, the individual shall either agree to
participate or if refusing, shall be under order of a court of appropriate
jurisdiction to have a screening.
a. The LDSS or LHD in receipt of the request for a
screening shall contact the individual or his representative within seven days
of the request date for screening to schedule a screening with the individual
and any other persons who the individual selects to attend the screening.
b. When the CBT has not scheduled a screening to occur
within 21 days of the request date for screening, and the screening is not
anticipated to be complete within 30 days of the request date for screening due
to the screening entity's inability to conduct the screening, the LDSS and LHD
shall, no later than seven days of the request date for screening, notify DARS
and VDH staff designated for technical assistance. After contact with the LDSS
and LHD, if DARS and VDH confirm that the screening entity is unable to
complete the screening within 30 days of the request date for screening, the
designated VDH staff shall refer the CBT and screening request to the DMAS
designee for scheduling of a screening and submission of documentation.
2. Referrals for screenings may also be accepted by LDSS or
LHD from an interested person having knowledge of an individual who may need
LTSS. When the LDSS or LHD receives such a referral, the LDSS or LHD shall
obtain sufficient information from the referral source to initiate contact with
the individual or his representative to discuss the PAS process. Within seven
days of the referral date, the LDSS or LHD shall contact the individual or his
representative to determine if the individual is interested in receiving LTSS
and would participate in the screening. If the LDSS or LHD is unable to contact
the individual or his representative, it shall document the attempt to contact
the individual or his representative using the method adopted by the CBT.
a. After contact with the individual or his representative,
or if the LDSS or LHD is unable to contact the individual or his
representative, the LDSS or LHD shall advise the referring interested person
that contact or attempt to contact has been made in response to the referral
for screening.
b. Information about the results of the contact shall be
shared with the interested person who made the referral only with either the
individual's written consent or the written consent of his legal representative
who has such authority on behalf of the individual.
B. Screenings for children living in the community.
Screenings for children who are residing in the community shall be completed
and submitted to the DMAS automated system within 30 days of the request date
for screening.
1. A child who is residing in the community and is not an
inpatient in an acute care hospital, rehabilitation unit of an acute care
hospital, or a rehabilitation hospital, and who may need LTSS, shall receive a
screening from a DMAS designee. Local CBTs shall forward requests for such
screenings directly to the DMAS designee.
2. The request for screening of a child residing in the
community shall initiate from the parent, the entity having legal custody of
that child, an emancipated child, or a child protective services worker having
an interest in the child.
3. Upon receipt of such a request, the DMAS designee shall
schedule an appointment to complete the screening. Community settings where
screenings may occur include the child's residence, other residences,
children's residential facilities, or other settings with the exception of
acute care hospitals, rehabilitation units of acute care hospitals, and
rehabilitation hospitals.
4. Referrals for screenings may also be accepted from an
interested person having knowledge of a child who may need LTSS. The same
process and timing and limitations on the sharing of the results shall apply to
such referrals for screenings for children as set out for adults.
C. Screening in hospitals for adults and children who are
inpatients. Screening in hospitals shall be completed when an adult or child
who is an inpatient may need LTSS upon discharge.
1. As a part of the discharge planning process, the
hospital team shall complete a screening when:
a. The individual's physician, in collaboration with the
individual, the individual's representative, if there is one, parent, entity
having legal custody, the managed care organization's care manager, or
emancipated child makes a request of the hospital team; or
b. The individual, the individual's representative, if
there is one, parent, entity having legal custody, the managed care
organization's care manager, or emancipated child requests a consultation with
hospital case management.
2. Such individual shall receive a screening conducted by
the hospital team regardless of the primary payer source (e.g., Medicare,
health maintenance organization) and whether or not they are eligible for
Medicaid or are anticipated to become eligible for Medicaid within six months
after admission to a NF.
12VAC30-60-305. Screenings in the community and hospitals
for Medicaid-funded long-term services and supports.
A. Community screenings for adults.
1. Eligibility for Medicaid-funded long-term services and
supports (LTSS) shall be determined by the community-based team (CBT) after
completion of a screening of the individual's needs and available supports. The
CBT shall document a screening of all the supports available for that
individual in the community (i.e., the immediate family, other relatives, other
community resources, and other services in the continuum of LTSS).
2. Screenings shall be completed in the individual's
residence unless the residence presents a safety risk for the individual or the
CBT, or unless the individual or the representative requests that the screening
be performed in an alternate location within the same jurisdiction. The
individual shall be permitted to have another person or persons present at the
time of the screening. The CBT shall determine the appropriate degree of
participation and assistance given by other persons to the individual during
the screening and accommodate the individual's preferences to the extent
feasible.
3. The CBT shall:
a. Observe the individual's ability to perform ADLs
according to 12VAC30-60-303 and consider the individual's communication or
responses to questions or his representative's communication or responses;
b. Observe and assess the individual's medical condition to
ensure accurate evaluation of the individual's need for modification of
treatment or additional medical procedures to prevent destabilization even when
the individual has demonstrated an inability to self-observe or evaluate the
need to contact skilled medical professionals; and
c. Identify the medical or nursing needs, or both, of the
individual.
4. The CBT shall consider services and settings that may be
needed by the individual in order for the individual to safely perform ADLs.
5. Upon completion of the screening and in consideration of
the communication from the individual, his representative, if appropriate, and
observations obtained during the screening, the CBT shall determine whether the
individual meets the criteria set out in 12VAC30-60-303. If the individual
meets the criteria for LTSS, the CBT shall inform and provide choice to the
individual and his representative, if appropriate, of the feasible alternatives
available through waiver services, PACE where appropriate and available, or
placement in a NF. If waiver services or PACE, where available, are declined,
the reason for the declination shall be recorded on the DMAS-97, Individual
Choice, Institutional Care, or Waiver Services form. The CBT shall have this
document signed by either the individual or his representative, if appropriate.
In addition to the electronic document, a paper copy of the DMAS-97 form with
the individual's or his representative's signature shall be retained in the
individual's record by the screening entity.
6. If the individual meets criteria selects community-based
services, the CBT shall also document that the individual is at risk of NF
placement in the absence of waiver services by finding that at least one of the
following conditions exists:
a. The individual has been cared for in the home prior to
the screening and evidence is available demonstrating a deterioration in the
individual's health care condition or a change in available supports preventing
former services and supports from meeting the individual's needs. Examples of
such evidence may include (i) recent hospitalizations, (ii) attending physician
documentation, or (iii) reported findings from medical or social service
agencies.
b. There has been no change in condition or available
support but evidence is available that demonstrates the individual's
functional, medical, or nursing needs are not being met. Examples of such
evidence may include (i) recent hospitalizations, (ii) attending physician
documentation, or (iii) reported findings from medical or social service
agencies.
7. If the individual selects NF placement, the CBT shall
complete a Level I screening, on the DMAS-95 Level I form, for mental illness,
intellectual disability, or related condition as required by § 1919(e)(7)
of the Social Security Act. When the Level I screening indicates that the
individual may have mental illness, intellectual disability, or related condition
or conditions, the CBT shall refer the individual to DBHDS for a Level II
screening.
a. DBHDS shall perform the Level II screening, documenting
it on the DMAS-95 Level II form.
b. DBHDS shall determine if the individual may benefit from
additional specialized services upon NF placement. DBHDS shall provide the
outcome of its Level II screening to the CBT for NF placements only.
c. The CBT shall provide the outcome of the Level II
screening to the NF that admits the individual and agrees to provide the
required specialized services indicated by the Level II outcome. The individual
shall be permitted to exercise choice among Medicaid-funded LTSS programs
throughout the process.
8. If the CBT determines that the individual does not meet
the criteria set out in 12VAC30-60-303, the CBT shall notify in writing the
individual and family/caregiver, as may be appropriate, that LTSS are being
denied for the individual. The denial notice shall include the individual's
right to appeal consistent with DMAS client appeals regulations (12VAC30-110).
B. Community screenings for children.
1. Eligibility for Medicaid-funded LTSS shall be determined
by the DMAS designee. The DMAS designee shall document a complete assessment of
the child's needs and available supports. The assessment shall be documented on
the designated DMAS forms identified in 12VAC30-60-306. If the child meets
criteria defined in 12VAC30-60-303, the DMAS designee shall provide the parent
or entity having legal custody of the child, or the emancipated child, the choice
of waiver services or nursing facility placement.
2. The DMAS designee shall determine the appropriate degree
of participation and assistance given by other persons to the individual during
the screening in recognition of the individual's preferences to the extent
feasible.
3. The DMAS designee shall:
a. Observe the child's ability to perform ADLs according to
12VAC30-60-303 and consider the parent's, legal guardian's, or emancipated
child's communications or responses to questions;
b. Observe and assess the child's medical condition to
assure accurate evaluation of the child's need for modification of treatment or
additional medical procedures to prevent destabilization even when the child
has demonstrated an inability to self-observe or evaluate the need to contact
skilled medical professionals; and
c. Identify the medical or nursing needs, or both, of the
child.
4. The DMAS designee shall consider services and settings
that may be needed by the child in order for the child to safely perform ADLs.
5. Upon completion of the screening and in consideration of
the communication from the individual, his representative, if appropriate, and
observations obtained during the screening, the DMAS designee shall determine
whether the individual meets the criteria set out in 12VAC30-60-303. If the
individual meets the criteria for LTSS, the DMAS designee shall inform and
provide choice to the individual and his representative, if appropriate, of the
feasible alternatives available through waiver services, PACE where appropriate
and available, or placement in a NF. If waiver services or PACE, where
available, are declined, the reason for declining shall be recorded on the
DMAS-97, Individual Choice, Institutional Care or Waiver Services form. The
DMAS designee shall have this document signed by either the individual or his
representative, if appropriate. In addition to the electronic document, a paper
copy of the DMAS-97 form with the individual's or his representative's
signature shall be retained in the individual's record by the screening entity.
6. If the individual who meets criteria selects
community-based services, the CBT shall also document that the individual is at
risk of NF placement in the absence of waiver services by finding that at least
one of the following conditions exists:
a. The individual has been cared for in the home prior to
the screening and evidence is available demonstrating a deterioration in the
individual's health care condition or a change in available supports preventing
former services and supports from meeting the individual's needs. Examples of
such evidence may include (i) recent hospitalizations, (ii) attending physician
documentation, or (iii) reported findings from medical or social service
agencies.
b. There has been no change in condition or available
support but evidence is available that demonstrates the individual's
functional, medical, or nursing needs are not being met. Examples of such
evidence may include (i) recent hospitalizations, (ii) attending physician
documentation, or (iii) reported findings from medical or social service
agencies.
7. If the parent, entity having legal custody of the child,
or emancipated child selects NF placement, the DMAS designee shall complete a
Level I screening, on the DMAS-95 Level I form, for mental illness,
intellectual disability, or related condition as required by § 1919(e)(7)
of the Social Security Act. When the Level I screening indicates that the child
may have mental illness, intellectual disability, or related condition, the
DMAS designee shall refer the child to DBHDS for a Level II screening.
a. DBHDS shall perform the Level II screening, documenting
it on the DMAS-95 Level II form.
b. DBHDS shall determine if the child may benefit from
additional specialized services upon NF placement. DBHDS shall provide the
outcome of its Level II screening to the DMAS designee.
c. The DMAS designee shall provide the outcome of the Level
II screening to the NF that admits the child and agrees to provide the required
specialized services indicated by the Level II outcome. The child, parent,
entity having legal custody, or emancipated child shall be permitted to
exercise choice among Medicaid-funded LTSS programs throughout the process.
8. If the DMAS designee determines that the child does not
meet the criteria to receive LTSS as set out in 12VAC30-60-303, the DMAS
designee shall notify in writing the parent, entity having legal custody of the
child, or the emancipated child and family/caregiver, as may be appropriate,
that LTSS are being denied for the child. The denial notice shall include the
child's right to appeal consistent with DMAS client appeals regulations
(12VAC30-110).
C. Screenings for adults and children in hospitals. For
the purpose of this subsection, the term "individual" shall mean
either an adult or a child.
1. Eligibility for Medicaid-funded LTSS for individuals who
are inpatients shall be determined by the hospital screening team, which shall
document a complete assessment of the individual's needs and available
supports.
2. Screenings shall be completed in the hospital prior to
discharge. The individual shall be permitted to have another person present at
the time of the screening. The hospital screening team shall determine the
appropriate degree of participation and assistance given by other persons to
the individual during the screening.
3. The hospital screening team shall:
a. Observe the individual's ability to perform ADLs
according to 12VAC30-60-303, excluding all institutionally induced
dependencies, and consider the individual's communication or responses to
questions, or his representative's communications or responses to questions;
b. Observe and assess the individual's medical condition to
ensure accurate evaluation of the individual's need for modification of treatment
or additional medical procedures or services to prevent destabilization even
when an individual has demonstrated an inability to self-observe or evaluate
the need to contact skilled medical professionals; and
c. Identify the medical or nursing needs, or both, of the
individual.
4. In developing the individual's discharge plans, the
hospital screening team shall consider services and settings that may be needed
by the individual in order for him to safely perform ADLs.
5. Upon completion of the screening and in consideration of
the communication from the individual, his representative, if appropriate, and
observations obtained during the screening, the hospital screening team shall
determine whether the individual meets the criteria set out in 12VAC30-60-303.
If the individual meets the criteria for LTSS, the hospital screening team
shall inform and provide choice to the individual and his representative, if
appropriate, of the feasible alternatives available through waiver services,
PACE where appropriate and available, or placement in a NF. If waiver services
or PACE, where available, are declined, the reason for declining shall be
recorded on the DMAS-97, Individual Choice, Institutional Care or Waiver
Services form. The hospital screening team shall have this document signed by
either the individual or his representative, if appropriate. In addition to the
electronic document, a paper copy of the DMAS-97 form with the individual's or
his representative's signature shall be retained in the individual's record by
the hospital screening team.
6. If the individual or his representative, if appropriate,
selects NF placement, the hospital screening team shall complete a Level I
screening, on the DMAS-95 Level I form, for mental illness, intellectual
disability, or related condition as required by § 1919(e)(7) of the Social
Security Act. When the Level I screening indicates the presence of mental
illness, intellectual disability, or related condition, the hospital screening
team shall refer the individual to DBHDS for a Level II screening prior to
discharge to determine if the individual may benefit from additional
specialized services upon NF admission.
a. DBHDS shall perform the Level II screening, documenting
it on the DMAS-95 Level II form.
b. DBHDS shall determine if the individual may benefit from
additional specialized services upon NF placement. DBHDS shall provide the
outcome of its Level II screening on the DMAS-95 Level I (MI/MR/RC) and if
appropriate, the DMAS-95 Level II form for NF placements only.
c. The hospital screening team shall provide the outcome of
the Level II screening to the NF that admits the individual and agrees to
provide the required specialized services indicated by the Level II outcome.
The individual or his representative, as appropriate, shall be permitted to
exercise choice among Medicaid-funded LTSS programs throughout the process.
7. If the hospital screening team determines that the
individual does not meet the criteria for LTSS set out in 12VAC30-60-303, the
hospital screening team shall notify in writing the individual and
family/caregiver, as may be appropriate, that LTSS are being denied for the
individual. The denial notice shall include the individual's right to appeal
consistent with DMAS client appeals regulations (12VAC30-110).
12VAC30-60-306. Submission of screenings.
A. The screening entity shall complete and submit the following
forms to DMAS electronically on ePAS:
1. DMAS 95 - MI/MR/ID/RC (Supplemental Assessment Process
Form Level I);
2. DMAS - 96 (Medicaid-Funded Long-Term Care Service
Authorization Form), as appropriate;
3. DMAS - 97 (Individual Choice – Institutional Care or
Waiver Services);
4. DMAS - 95 MI/MR Supplement II; and
5. UAI (Uniform Assessment Instrument).
B. For screenings performed in the community, the
screening entity shall submit to DMAS on ePAS each PAS form listed in
subsection A of this section within 30 days of the individual's request date
for screening.
C. For screenings performed in a hospital, the hospital
team shall submit to DMAS on ePAS each screening form listed in subsection A of
this section, which shall be completed prior to the individual's discharge. For
individuals who will be admitted to a Medicare-funded skilled NF or to a
Medicare-funded rehabilitation hospital (or rehabilitation unit) directly upon
discharge from the hospital, the hospital screener shall have up to an additional
three days post-discharge to submit the screening forms via ePAS.
12VAC30-60-307. Summary of pre-admission nursing facility
criteria. (Repealed.)
A. An individual shall be determined to meet the nursing
facility criteria when:
1. The individual has both limited functional capacity and
requires medical or nursing management according to the requirements of
12VAC30-60-303, or
2. The individual is rated dependent in some functional
limitations, but does not meet the functional capacity requirements, and the
individual requires the daily direct services or supervision of a licensed
nurse that cannot be managed on an outpatient basis (e.g., clinic, physician
visits, home health services).
B. An individual shall not be determined to meet nursing
facility criteria when one of the following specific care needs solely
describes his or her condition:
1. An individual who requires minimal assistance with
activities of daily living, including those persons whose only need in all
areas of functional capacity is for prompting to complete the activity;
2. An individual who independently uses mechanical devices
such as a wheelchair, walker, crutch, or cane;
3. An individual who requires limited diets such as a
mechanically altered, low salt, low residue, diabetic, reducing, and other
restrictive diets;
4. An individual who requires medications that can be
independently self-administered or administered by the caregiver;
5. An individual who requires protection to prevent him
from obtaining alcohol or drugs or to address a social or environmental
problem;
6. An individual who requires minimal staff observation or
assistance for confusion, memory impairment, or poor judgment;
7. An individual whose primary need is for behavioral
management which can be provided in a community-based setting;
12VAC30-60-308. Nursing facility admission and level of care
determination requirements.
A. Prior to an individual's admission, the NF shall review
the completed preadmission screening forms to ensure that applicable NF admission
criteria have been met and documented.
B. The Department of Medical Assistance Services shall
conduct reviews of Minimum Data Set individuals' data submitted by NFs.
12VAC30-60-310. ePAS requirements and submission.
[Reserved]
12VAC30-60-312. Evaluation to determine eligibility for
Medicaid payment of nursing facility or home and community-based care services.
(Repealed.)
A. The screening team shall not authorize Medicaid-funded
nursing facility services for any individual who does not meet nursing facility
criteria. Once the nursing home preadmission screening team has determined
whether or not an individual meets the nursing facility criteria, the screening
team must determine the most appropriate and cost-effective means of meeting
the needs of the individual. The screening team must document a complete
assessment of all the resources available for that individual in the community
(i.e., the immediate family, other relatives, other community resources and
other services in the continuum of long-term care which are less intensive than
nursing facility level-of-care services). The screening team shall be
responsible for preauthorizing Medicaid-funded long-term care according to the
needs of each individual and the support required to meet those needs. The
screening team shall authorize Medicaid-funded nursing facility care for an
individual who meets the nursing facility criteria only when services in the
community are either not a feasible alternative or the individual or the
individual's representative rejects the screening team's plan for community
services. The screening team must document that the option of community-based
alternatives has been explained, the reason community-based services were not
chosen, and have this document signed by the client or client's primary
caregivers.
B. The screening team shall authorize community-based
waiver services only for an individual who meets the nursing facility criteria
and is at risk of nursing home placement without waiver services. Waiver
services are offered to such an individual as an alternative to avoid nursing
facility admission pursuant to 42 CFR 441.302 (c)(1).
C. Federal regulations which govern Medicaid-funded home
and community-based services require that services only be offered to
individuals who would otherwise require institutional placement in the absence
of home- and community-based services. The determination that an individual
would otherwise require placement in a nursing facility is based upon a finding
that the individual's current condition and available support are insufficient
to enable the individual to remain in the home and thus the individual is at
risk of institutionalization if community-based care is not authorized. The
determination of the individual's risk of nursing facility placement shall be
documented either on the state-designated pre-admission screening assessment or
in a separate attachment for every individual authorized to receive
community-based waiver services. To authorize community-based waiver services,
the screening team must document that the individual is at risk of nursing
facility placement by finding that one of the following conditions is met:
1. Application for the individual to a nursing facility has
been made and accepted;
2. The individual has been cared for in the home prior to
the assessment and evidence is available demonstrating a deterioration in the
individual's health care condition or a change in available support preventing
former care arrangements from meeting the individual's need. Examples of such
evidence may be, but shall not necessarily be limited to:
a. Recent hospitalizations;
b. Attending physician documentation; or
c. Reported findings from medical or social service
agencies.
3. There has been no change in condition or available
support but evidence is available that demonstrates the individual's
functional, medical and nursing needs are not being met. Examples of such
evidence may be, but shall not necessarily be limited to:
a. Recent hospitalizations;
b. Attending physician documentation; or
c. Reported findings from medical or social service
agencies.
12VAC30-60-313. Individuals determined to not meet criteria
for Medicaid-funded long-term services and supports.
An individual shall be determined not to meet criteria for
Medicaid-funded LTSS when one of the following specific care needs solely
describes the individual's condition:
1. The individual requires minimal assistance with ADLs,
including those individuals whose only need in all areas of functional capacity
is for prompting to complete the activity;
2. The individual independently uses mechanical devices
such as a wheelchair, walker, crutch, or cane;
3. The individual requires limited diets such as a
mechanically altered, low-salt, low-residue, diabetic, reducing, and other
restrictive diets;
4. The individual requires medications that can be
independently self-administered or administered by the caregiver;
5. The individual requires protection to prevent him from
obtaining alcohol or drugs or to address a social or environmental problem;
6. The individual requires minimal staff observation or
assistance for confusion, memory impairment, or poor judgment; or
7. The individual's primary need is for behavioral management
that can be provided in a community-based setting.
12VAC30-60-315. Ongoing evaluations for individuals
receiving Medicaid-funded long-term services and supports.
A. Once an individual is admitted to community-based
services, the CBS provider shall be responsible for conducting ongoing
evaluations to ensure that the individual meets, and continues to meet, the
waiver program or PACE criteria. These ongoing evaluations shall be conducted
using the Level of Care form (DMAS 99 LOC).
B. Once an individual is admitted to a NF, the NF shall be
responsible for conducting ongoing evaluations to ensure that the individual
meets, and continues to meet, the NF criteria. For this purpose, the NF shall
use the federally required Minimum Data Set (MDS) form. The post-admission
evaluation shall be conducted no later than 14 days after the date of NF
admission and promptly after an individual's significant change in
circumstances.
C. For individuals who are enrolled in a managed care
organization (MCO) that is responsible for providing LTSS, the MCO shall
conduct ongoing evaluations by qualified MCO staff to ensure the individual
continues to meet criteria for LTSS.
NOTICE: The following
forms used in administering the regulation were filed by the agency. The forms
are not being published; however, online users of this issue of the Virginia
Register of Regulations may click on the name of a form with a hyperlink to
access it. The forms are also available from the agency contact or may be
viewed at the Office of the Registrar of Regulations, General Assembly
Building, 2nd Floor, Richmond, Virginia 23219.
FORMS (12VAC30-60)
Certificate of Medical Necessity -- Durable Medical Equipment
and Supplies, DMAS 352 (rev. 8/95).
Request for Hospice Benefits, DMAS 420 (rev. 1/99).
Screening
for Mental Illness, Mental Retardation/Intellectual Disability, or Related
Conditions, DMAS-95/IDD/RC (rev. 12/2015)
Medicaid
Funded Long-Term Services and Supports Authorization Form, DMAS-96 (rev.
12/2015)
Individual
Choice - Institutional Care or Waiver Services Form, DMAS-97 (rev. 8/2012)
Virginia
Uniform Assessment Instrument
Virginia
Uniform Assessment Instrument, DMAS-98 (eff. 2/2016), including:
UAI-A; UAI-B; Eligibility Communication Document; Screening
for Mental Illness, Mental Retardation/Intellectual Disability, or Related Conditions;
MI/MR Supplemental: Level II; Medicaid Funded Long-Term Care Service
Authorization Form; Individual Choice - Institutional Care or Waiver Services
Form; and Attachment to Public Pay Short Form Assessment
Community-Based
Care Level of Care Review Instrument, DMAS-99LOC (undated)
VA.R. Doc. No. R16-4355; Filed June 21, 2016, 10:25 a.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Final Regulation
Title of Regulation: 12VAC30-80. Methods and
Standards for Establishing Payment Rates; Other Types of Care (amending 12VAC30-80-20, 12VAC30-80-40; adding
12VAC30-80-36).
Statutory Authority: § 32.1-325 of the Code of Virginia.
Effective Date: August 10, 2016.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, 600 East Broad Street, Suite 1300,
Richmond, VA 23219, telephone (804) 371-4300, FAX (804) 786-1680, or email
emily.mcclellan@dmas.virginia.gov.
Summary:
The amendments implement a prospective payment methodology
for Medicaid outpatient hospital services as provided in Item 301 TT of Chapter
3 of the 2014 Acts of Assembly, Special Session I. The enhanced ambulatory
patient group (EAPG) reimbursement methodology for outpatient hospital
services, which is currently in place through emergency regulations, assigns
outpatient procedures and ancillary services that reflect similar patient
characteristics and resource utilization to EAPG codes.
Summary of Public Comments and Agency's Response: No
public comments were received by the promulgating agency.
12VAC30-80-20. Services that are reimbursed on a cost basis.
A. Payments for services listed below in this
section shall be on the basis of reasonable cost following the standards
and principles applicable to the Title XVIII Program with the exception provided
for in subdivision D 1 d e of this section. The upper limit for
reimbursement shall be no higher than payments for Medicare patients on a
facility by facility basis in accordance with 42 CFR 447.321 and 42 CFR
447.325. In no instance, however, shall charges for beneficiaries of the
program be in excess of charges for private patients receiving services from
the provider. The professional component for emergency room physicians shall
continue to be uncovered as a component of the payment to the facility.
B. Reasonable costs will be determined from the filing of a
uniform cost report by participating providers. The cost reports are due not
later than 150 days after the provider's fiscal year end. If a complete cost
report is not received within 150 days after the end of the provider's fiscal
year, the Program shall take action in accordance with its policies to assure
that an overpayment is not being made. The cost report will be judged complete
when DMAS has all of the following:
1. Completed cost reporting [ form(s) form ]
provided by DMAS, with signed [ certification(s) certification ];
2. The provider's trial balance showing adjusting journal
entries;
3. The provider's financial statements including, but not
limited to, a balance sheet, a statement of income and expenses, a statement of
retained earnings (or fund balance), and a statement of changes in financial
position;
4. Schedules that reconcile financial statements and trial
balance to expenses claimed in the cost report;
5. Depreciation schedule or summary;
6. Home office cost report, if applicable; and
7. Such other analytical information or supporting documents
requested by DMAS when the cost reporting forms are sent to the provider.
C. Item 398 D of the 1987 Appropriation Act (as amended),
effective April 8, 1987, eliminated reimbursement of return on equity capital
to proprietary providers.
D. The services that are cost reimbursed are:
1. Outpatient For dates of service prior to January
1, 2014, outpatient hospital services, including rehabilitation hospital
outpatient services and excluding laboratory services.
a. Definitions. The following words and terms when used in
this regulation shall have the following meanings when applied to emergency
services unless the context clearly indicates otherwise:
"All-inclusive" means all emergency department and
ancillary service charges claimed in association with the emergency room visit,
with the exception of laboratory services.
"DMAS" means the Department of Medical Assistance
Services consistent with Chapter 10 (§ 32.1-323 et seq.) of Title 32.1 of the
Code of Virginia.
"Emergency hospital services" means services that
are necessary to prevent the death or serious impairment of the health of the
recipient. The threat to the life or health of the recipient necessitates the
use of the most accessible hospital available that is equipped to furnish the
services.
"Recent injury" means an injury that has occurred
less than 72 hours prior to the emergency department visit.
b. Scope. DMAS shall differentiate, as determined by the
attending physician's diagnosis, the kinds of care routinely rendered in
emergency departments and reimburse for nonemergency care rendered in emergency
departments at a reduced rate.
(1) With the exception of laboratory services, DMAS shall
reimburse at a reduced and all-inclusive reimbursement rate for all services
rendered in emergency departments that DMAS determines were nonemergency care.
(2) Services determined by the attending physician to be
emergencies shall be reimbursed under the existing methodologies and at the
existing rates.
(3) Services performed by the attending physician that may be
emergencies shall be manually reviewed. If such services meet certain criteria,
they shall be paid under the methodology for subdivision 1 b (2) of this
subsection. Services not meeting certain criteria shall be paid under the
methodology of subdivision 1 b (1) of this subsection. Such criteria shall
include, but not be limited to:
(a) The initial treatment following a recent obvious injury.
(b) Treatment related to an injury sustained more than 72
hours prior to the visit with the deterioration of the symptoms to the point of
requiring medical treatment for stabilization.
(c) The initial treatment for medical emergencies including
indications of severe chest pain, dyspnea, gastrointestinal hemorrhage,
spontaneous abortion, loss of consciousness, status epilepticus, or other
conditions considered life threatening.
(d) A visit in which the recipient's condition requires immediate
hospital admission or the transfer to another facility for further treatment or
a visit in which the recipient dies.
(e) Services provided for acute vital sign changes as
specified in the provider manual.
(f) Services provided for severe pain when combined with one
or more of the other guidelines.
(4) Payment shall be determined based on ICD diagnosis codes
and necessary supporting documentation. As used here, the term "ICD"
is defined in 12VAC30-95-5.
(5) DMAS shall review on an ongoing basis the effectiveness of
this program in achieving its objectives and for its effect on recipients,
physicians, and hospitals. Program components may be revised subject to
achieving program intent, the accuracy and effectiveness of the ICD code
designations, and the impact on recipients and providers. As used here, the
term "ICD" is defined in 12VAC30-95-5.
c. Limitation of allowable cost. Effective for services on and
after July 1, 2003, reimbursement of Type Two hospitals for outpatient services
shall be at various percentages as noted in subdivisions 1 c (1) and 1 c (2) of
this subsection of allowable cost, with cost to be determined as provided in
subsections A, B, and C of this section. For hospitals with fiscal years that
do not begin on July 1, outpatient costs, both operating and capital, for the
fiscal year in progress on that date shall be apportioned between the time
period before and the time period after that date, based on the number of
calendar months in the cost reporting period, falling before and after that
date.
(1) Type One hospitals.
(a) Effective July 1, 2003, through June 30, 2010, hospital
outpatient operating reimbursement shall be at 94.2% of allowable cost and
capital reimbursement shall be at 90% of allowable cost.
(b) Effective July 1, 2010, through September 30, 2010,
hospital outpatient operating reimbursement shall be at 91.2% of allowable cost
and capital reimbursement shall be at 87% of allowable cost.
(c) Effective October 1, 2010, through June 30, 2011, hospital
outpatient operating reimbursement shall be at 94.2% of allowable cost and
capital reimbursement shall be at 90% of allowable cost.
(d) Effective July 1, 2011, hospital outpatient operating
reimbursement shall be at 90.2% of allowable cost and capital reimbursement
shall be at 86% of allowable cost.
(2) Type Two hospitals.
(a) Effective July 1, 2003, through June 30, 2010, hospital
outpatient operating and capital reimbursement shall be 80% of allowable cost.
(b) Effective July 1, 2010, through September 30, 2010,
hospital outpatient operating and capital reimbursement shall be 77% of
allowable cost.
(c) Effective October 1, 2010, through June 30, 2011, hospital
outpatient operating and capital reimbursement shall be 80% of allowable cost.
(d) Effective July 1, 2011, hospital outpatient operating and
capital reimbursement shall be 76% of allowable cost.
d. The last cost report with a fiscal year end on or after
December 31, 2013, shall be used for reimbursement for dates of service through
December 31, 2013, based on this section. Reimbursement shall be based on
charges reported for dates of service prior to January 1, 2014. Settlement will
be based on four months of runout from the end of the provider's fiscal year.
Claims for services paid after the cost report runout period will not be
settled.
e. Payment for direct medical education costs of
nursing schools, paramedical programs and graduate medical education for
interns and residents.
(1) Direct medical education costs of nursing schools and
paramedical programs shall continue to be paid on an allowable cost basis.
(2) Effective with cost reporting periods beginning on or
after July 1, 2002, direct graduate medical education (GME) costs for interns
and residents shall be reimbursed on a per-resident prospective basis. See
12VAC30-70-281 for prospective payment methodology for graduate medical
education for interns and residents.
2. Rehabilitation agencies or comprehensive outpatient
rehabilitation.
a. Effective July 1, 2009, rehabilitation agencies or
comprehensive outpatient rehabilitation facilities that are operated by
community services boards or state agencies shall be reimbursed their costs.
For reimbursement methodology applicable to all other rehabilitation agencies,
see 12VAC30-80-200.
b. Effective October 1, 2009, rehabilitation agencies or
comprehensive outpatient rehabilitation facilities operated by state agencies
shall be reimbursed their costs. For reimbursement methodology applicable to
all other rehabilitation agencies, see 12VAC30-80-200.
12VAC30-80-36. Fee-for-service providers: outpatient
hospitals.
A. Definitions. The following words and terms when used in
this section shall have the following meanings unless the context clearly
indicates otherwise:
"Enhanced ambulatory patient group" or
"EAPG" means a defined group of outpatient procedures, encounters, or
ancillary services that incorporates International Classification of Diseases
(ICD) diagnosis codes, Current Procedural Terminology (CPT) codes, and
Healthcare Common Procedure Coding System (HCPCS) codes.
"EAPG relative weight" means the expected
average costs for each EAPG divided by the relative expected average costs for
visits assigned to all EAPGs.
"Base year" means the state fiscal year for
which data is used to establish the EAPG base rate. The base year will change
when the EAPG payment system is rebased and recalibrated. In subsequent
rebasings, [ the Commonwealth DMAS ] shall
notify affected providers of the base year to be used in this calculation.
"Cost" means the reported cost as described in
12VAC30-80-20 A and B.
"Cost-to-charge ratio" equals the hospital's
total costs divided by the hospital's total charges. The Cost-to-charge ratio
shall be calculated using data from cost reports from hospital fiscal years
ending in the state fiscal year used as the base year.
"Medicare wage index" means the Medicare wage
index published annually in the Federal Register by the Centers for Medicare
and Medicaid Services. The indices used in this section shall be those in
effect in the base year.
B. Effective January 1, 2014, the prospective enhanced
ambulatory patient group (EAPG) based payment system described in this
subsection shall apply to reimbursement for outpatient hospital services (with
the exception of laboratory services referred to the hospital but not
associated with an outpatient hospital visit, which will be reimbursed
according to the laboratory fee schedule).
1. The payments for outpatient hospital visits shall be
determined on the basis of a hospital-specific base rate per visit multiplied
by the relative weight of the EAPG (and the payment action) assigned for each
of the services performed during a hospital visit.
2. The EAPG relative weights shall be the weights
determined and published periodically by DMAS and shall be consistent with
applicable Medicaid reimbursement limits and policies. The weights shall be
updated at least every three years.
3. The statewide base rate shall be equal to the total
costs described in this subdivision divided by the wage-adjusted sum of the
EAPG weights for each facility. The wage-adjusted sum of the EAPG weights shall
equal the sum of the EAPG weights multiplied by the labor percentage times
the hospital's Medicare wage index plus the sum of the EAPG weights multiplied
by the nonlabor percentage. The base rate shall be determined for outpatient
hospital services at least every three years so that total expenditures will
equal the following:
a. When using base years prior to January 1, 2014, for all
services, excluding all laboratory services and emergency services described in
subdivision 3 c of this subsection, a percentage of costs as reported in the
available cost reports for the base period for each type of hospital as defined
in 12VAC30-70-221.
(1) Type One hospitals. Effective January 1, 2014, hospital
outpatient operating reimbursement shall be calculated at 90.2% of cost, and
capital reimbursement shall be at 86% of cost inflated to the rate year.
(2) Type Two hospitals. Effective January 1, 2014, hospital
outpatient operating and capital reimbursement shall be calculated at 76% of
cost inflated to the rate year.
When using base years after January 1, 2014, the
percentages described in subdivision 3 a of this subsection shall be adjusted
according to subdivision 3 c of this subsection.
b. Laboratory services, excluding laboratory services
referred to the hospital but not associated with a hospital visit, are
calculated at the fee schedule in effect for the rate year.
c. Services rendered in emergency departments determined to
be nonemergencies as prescribed in 12VAC30-80-20 D 1 b shall be calculated at
the nonemergency reduced rate reported in the base year for base years prior to
January 1, 2014. For base years after January 1, 2014, the cost percentages in
subdivision 3 a of this subsection shall be adjusted to reflect services paid
at the nonemergency reduced rate in the last [ base ]
year prior to January 1, 2014.
4. Inflation adjustment to base year costs. Each July, the
Virginia moving average values as compiled and published by Global Insight (or
its successor), under contract with DMAS, shall be used to update the base year
costs to the midpoint of the rate year. The most current table available prior
to the effective date of the new rates shall be used to inflate base year
amounts to the upcoming rate year. Thus, corrections made by Global Insight (or
its successor) in the moving averages that were used to update rates for
previous state fiscal years shall be automatically incorporated into the moving
averages that are being used to update rates for the upcoming state fiscal
year. Inflation shall be applied to the costs identified in subdivision 3 a of
this subsection.
5. Hospital-specific base rate. The hospital-specific base
rate per case shall be adjusted for geographic variation. The hospital-specific
base rate shall be equal to the labor portion of the statewide base rate
multiplied by the hospital's Medicare wage index plus the nonlabor percentage
of the statewide base rate. The labor percentage shall be determined at each
rebasing based on the most recently reliable data. For rural hospitals, the
hospital's Medicare wage index used to calculate the base rate shall be the
Medicare wage index of the nearest metropolitan wage area or the effective
Medicare wage index, whichever is higher. A base rate differential of 5.0%
shall be established for freestanding Type Two children's hospitals. The base
rate for noncost-reporting hospitals shall be the average of the
hospital-specific base rates of in-state Type Two hospitals.
6. The total payment shall represent the total allowable
amount for a visit including ancillary services and capital.
7. The transition from cost-based reimbursement to EAPG
reimbursement shall be transitioned over a four-year period. DMAS shall
calculate a cost-based base rate at January 1, 2014, and at each rebasing
during the transition.
a. Effective for dates of service on or after January 1,
2014, DMAS shall calculate the hospital-specific base rate as the sum of 75% of
the cost-based base rate and 25% of the EAPG base rate.
b. Effective for dates of service on or after July 1, 2014,
DMAS shall calculate the hospital-specific base rate as the sum of 50% of the
cost-based base rate and 50% of the EAPG base rate.
c. Effective for dates of service on or after July 1, 2015,
DMAS shall calculate the hospital-specific base rate as the sum of 25% of the
cost-based base rate and 75% of the EAPG base rate.
d. Effective for dates of service on or after July 1, 2016,
DMAS shall calculate the hospital-specific base rate as the EAPG base rate.
8. To maintain budget neutrality during the first six years
of the transition to EAPG reimbursement, DMAS shall compare the total
reimbursement of hospital claims based on the parameters in subdivision 3 of
this subsection to EAPG reimbursement every six months based on the six months
of claims ending three months prior to the potential adjustment. If the
percentage difference between the reimbursement target in subdivision 3 of this
subsection and EAPG reimbursement is greater than 1.0%, plus or minus, DMAS
shall adjust the statewide base rate by the percentage difference the following
July 1 or January 1. The first possible adjustment would be January 1, 2015,
using reimbursement between January 1, 2014, and October 31, 2014.
C. The enhanced ambulatory patient group (EAPG) grouper
version used for outpatient hospital services shall be determined by DMAS.
Providers or provider representatives shall be given notice prior to
implementing a new grouper.
D. The primary data sources used in the development of the
EAPG payment methodology are the DMAS hospital computerized claims history file
and the cost report file. The claims history file captures available claims
data from all enrolled, cost-reporting general acute care hospitals. The cost
report file captures audited cost and charge data from all enrolled general
acute care hospitals. The following table identifies key data elements that are
used to develop the EAPG payment methodology. DMAS may supplement this data
with similar data for Medicaid services furnished by managed care organizations
if DMAS determines that it is reliable.
Data Elements for EAPG Payment Methodology
|
Data Elements
|
Source
|
Total charges for each outpatient hospital visit
|
Claims history file
|
Number of groupable claims lines in each EAPG
|
Claims history file
|
Total number of groupable claim lines
|
Claims history file
|
Total charges for each outpatient hospital revenue line
|
Claims history file
|
Total number of EAPG assignments
|
Claims history file
|
Cost-to-charge ratio for each hospital
|
Cost report file
|
Medicare wage index for each hospital
|
Federal Register
|
12VAC30-80-40. Fee-for-service providers: pharmacy.
Payment for pharmacy services (excluding outpatient
hospital) shall be the lowest of subdivisions 1 through 5 of this section
(except that subdivisions 1 and 2 of this section will not apply when
prescriptions are certified as brand necessary by the prescribing physician in
accordance with the procedures set forth in 42 CFR 447.512(c) if the brand cost
is greater than the Centers for Medicare and Medicaid Services (CMS) upper
limit of VMAC cost) subject to the conditions, where applicable, set forth in
subdivisions 6 and 7 of this section:
1. The upper limit established by the CMS for multiple source
drugs pursuant to 42 CFR 447.512 and 447.514, as determined by the CMS Upper
Limit List plus a dispensing fee. If the agency provides payment for any drugs
on the HCFA Upper Limit List, the payment shall be subject to the aggregate
upper limit payment test.
2. The methodology used to reimburse for generic drug products
shall be the higher of either (i) the lowest Wholesale Acquisition Cost (WAC)
plus 10% or (ii) the second lowest WAC plus 6.0%. This methodology shall reimburse
for products' costs based on a Maximum Allowable Cost (VMAC) list to be
established by the single state agency.
a. In developing the maximum allowable reimbursement rate for
generic pharmaceuticals, the department or its designated contractor shall:
(1) Identify three different suppliers, including
manufacturers that are able to supply pharmaceutical products in sufficient
quantities. The drugs considered must be listed as therapeutically and
pharmaceutically equivalent in the Food and Drug Administration's most recent
version of the Approved Drug Products with Therapeutic Equivalence Evaluations
(Orange Book). Pharmaceutical products that are not available from three
different suppliers, including manufacturers, shall not be subject to the VMAC
list.
(2) Identify that the use of a VMAC rate is lower than the
Federal Upper Limit (FUL) for the drug. The FUL is a known, widely published
price provided by CMS; and
(3) Distribute the list of state VMAC rates to pharmacy
providers in a timely manner prior to the implementation of VMAC rates and
subsequent modifications. DMAS shall publish on its website, each month, the
information used to set the Commonwealth's prospective VMAC rates, including,
but not necessarily limited to:
(a) The identity of applicable reference products used to set
the VMAC rates;
(b) The Generic Code Number (GCN) or National Drug Code (NDC),
as may be appropriate, of reference products;
(c) The difference by which the VMAC rate exceeds the
appropriate WAC price; and
(d) The identity and date of the published compendia used to
determine reference products and set the VMAC rate. The difference by which the
VMAC rate exceeds the appropriate WAC price shall be at least or equal to 10%
above the lowest-published wholesale acquisition cost for products widely
available for purchase in the Commonwealth and shall be included in national
pricing compendia.
b. Development of a VMAC rate that does not have a FUL rate
shall not result in the use of higher-cost innovator brand name or single
source drugs in the Medicaid program.
c. DMAS or its designated contractor shall:
(1) Implement and maintain a procedure to add or eliminate
products from the list, or modify VMAC rates, consistent with changes in the
fluctuating marketplace. DMAS or its designated contractor will regularly
review manufacturers' pricing and monitor drug availability in the marketplace
to determine the inclusion or exclusion of drugs on the VMAC list; and
(2) Provide a pricing dispute resolution procedure to allow a
dispensing provider to contest a listed VMAC rate. DMAS or its designated
contractor shall confirm receipt of pricing disputes within 24 hours, via
telephone or facsimile, with the appropriate documentation of relevant
information, e.g. for example, invoices. Disputes shall be
resolved within three business days of confirmation. The pricing dispute
resolution process will include DMAS' or the contractor's verification of
accurate pricing to ensure consistency with marketplace pricing and drug
availability. Providers will be reimbursed, as appropriate, based on findings.
Providers shall be required to use this dispute resolution process prior to
exercising any applicable appeal rights.
3. The provider's usual and customary charge to the public, as
identified by the claim charge.
4. The Estimated Acquisition Cost (EAC), which shall be based
on the published Average Wholesale Price (AWP) minus a percentage discount
established by the General Assembly (as set forth in subdivision 7 of this
section) or, in the absence thereof, by the following methodology set out in
subdivisions a through c of this subdivision.
a. Percentage discount shall be determined by a statewide
survey of providers' acquisition cost.
b. The survey shall reflect statistical analysis of actual
provider purchase invoices.
c. The agency will conduct surveys at intervals deemed
necessary by DMAS.
5. [ MAC Maximum allowable cost (MAC) ]
methodology for specialty drugs. Payment for drug products designated by DMAS
as specialty drugs shall be the lesser of subdivisions 1 through 4 of this
section or the following method, whichever is least:
a. The methodology used to reimburse for designated specialty
drug products shall be the WAC price plus the WAC percentage. The WAC
percentage is a constant percentage identified each year for all GCNs.
b. Designated specialty drug products are certain products
used to treat chronic, high-cost, or rare diseases; the drugs subject to this
pricing methodology and their current reimbursement rates are listed on the
DMAS website at the following internet address: http://www.dmas.virginia.gov/downloads/pdfs/pharm-special_mac_list.pdf
http://www.dmas.virginia.gov/Content_pgs/pharm-home.aspx.
c. The MAC reimbursement methodology for specialty drugs shall
be subject to the pricing review and dispute resolution procedures described in
subdivisions 2 c (1) and 2 c (2) of this section.
6. Payment for pharmacy services will be as described above
in subdivisions 1 through 5 of this section; however, payment for legend
drugs will include the allowed cost of the drug plus only one dispensing fee
per month for each specific drug. Exceptions to the monthly dispensing fees
shall be allowed for drugs determined by the department to have unique
dispensing requirements. The dispensing fee for brand name and generic drugs is
$3.75.
7. An EAC of AWP minus 13.1% shall become effective July 1,
2011. The dispensing fee for brand name and generic drugs of $3.75 shall remain
in effect, creating a payment methodology based on the previous algorithm
(least of subdivisions of this section) plus a dispensing fee where applicable.
8. Home infusion therapy.
a. The following therapy categories shall have a pharmacy
service day rate payment allowable: hydration therapy, chemotherapy, pain
management therapy, drug therapy, and total parenteral nutrition (TPN). The
service day rate payment for the pharmacy component shall apply to the basic
components and services intrinsic to the therapy category. Submission of claims
for the per diem rate shall be accomplished by use of the CMS 1500 claim form.
b. The cost of the active ingredient or ingredients for
chemotherapy, pain management, and drug therapies shall be submitted as
a separate claim through the pharmacy program, using standard pharmacy format.
Payment for this component shall be consistent with the current reimbursement
for pharmacy services. Multiple applications of the same therapy shall be
reimbursed one service day rate for the pharmacy services. Multiple
applications of different therapies shall be reimbursed at 100% of standard
pharmacy reimbursement for each active ingredient.
9. Supplemental rebate agreement. The Commonwealth complies
with the requirements of § 1927 of the Social Security Act and Subpart I
(42 CFR 447.500 et seq.) of 42 CFR Part 447 with
regard to supplemental drug rebates. In addition, the following requirements
are also met:
a. Supplemental drug rebates received by the state in excess
of those required under the national drug rebate agreement will be shared with
the federal government on the same percentage basis as applied under the
national drug rebate agreement.
b. Prior authorization requirements found in § 1927(d)(5) of
the Social Security Act have been met.
c. Nonpreferred drugs are those that were reviewed by the
Pharmacy and Therapeutics Committee and not included on the preferred drug
list. Nonpreferred drugs will be made available to Medicaid beneficiaries
through prior authorization.
d. Payment of supplemental rebates may result in a product's
inclusion on the PDL.
10. Each drug administered in an outpatient hospital
setting and reimbursed based on the enhanced ambulatory patient group methodology,
as described in 12VAC30-80-36, shall be reimbursed separately at a rate greater
than zero to be eligible for drug rebate claiming.
VA.R. Doc. No. R14-3799; Filed June 21, 2016, 10:17 a.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Notice of Extension of Emergency Regulation
Title of Regulation: 12VAC30-120. Waivered Services (amending 12VAC30-120-360 through 12VAC30-120-395,
12VAC30-120-410, 12VAC30-120-420).
Statutory Authority: § 32.1-325 of the Code of Virginia; 42 USC § 1396.
Expiration Date Extended Through: December 29, 2016.
The Governor has approved the Department of Medical Assistance
Services request to extend the expiration date of the above-referenced
emergency regulation for six months as provided for in § 2.2-4011 D of the
Code of Virginia. Therefore, the emergency regulation will continue in effect
through December 29, 2016. The emergency regulation implements several mandates
from various legislative actions to (i) require individuals who are
participating in a home and community-based care services waiver, specifically
the Elderly or Disabled with Consumer Direction Waiver, to also be enrolled in
Medicaid contracted managed care organizations and (ii) require expedited
enrollment for Medicaid individuals into Medicaid contracted managed care
organizations, especially for pregnant women. The emergency regulation was
published in 31:11 VA.R. 947-955 January 26, 2015,
and a final regulation to replace the emergency regulation was published in 32:22 VA.R. 2953-2961 June 27, 2016.
Contact Information: Victoria Simmons, Regulatory
Coordinator, Department of Medical Assistance Services, 600 East Broad Street,
Suite 1300, Richmond, VA 23219, telephone (804) 371-6043, FAX (804) 786-1680,
TTY (800) 343-0634, or email victoria.simmons@dmas.virginia.gov.
VA.R. Doc. No. R15-4135; Filed June 17, 2016, 5:22 p.m.
TITLE 12. HEALTH
DEPARTMENT OF MEDICAL ASSISTANCE SERVICES
Notice of Extension of Emergency Regulation
Title of Regulation: 12VAC30-135. Demonstration
Waiver Services (adding 12VAC30-135-400 through 12VAC30-135-498).
Statutory Authority: § 32.1-325 of the Code of
Virginia; § 1115 of the Social Security Act.
Expiration Date Extended Through: December 29, 2016.
The Governor has approved the Department of Medical Assistance
Services request to extend the expiration date of the above-referenced
emergency regulation for six months as provided for in § 2.2-4011 D of the
Code of Virginia. Therefore, the emergency regulation will continue in effect
through December 29, 2016. The emergency regulation established the Governor's
Access Plan Demonstration Waiver to improve access to health care for a segment
of the uninsured population in Virginia who have significant behavioral and
medical needs, improve health and behavioral health outcomes of participants in
this program, and serve as a bridge to closing the insurance coverage gap for
uninsured Virginians. The emergency regulation was published in 31:10 VA.R. 864-882 January 12, 2015,
and an amendment to certain sections of the emergency regulation was published
in 31:23 VA.R. 2128-2137 July 13, 2015.
Agency Contact: Emily McClellan, Regulatory Supervisor,
Department of Medical Assistance Services, 600 East Broad Street, Suite 1300,
Richmond, VA 23219, telephone (804) 371-4300, FAX (804) 786-1680, or email
emily.mcclellan@dmas.virginia.gov.
VA.R. Doc. No. R15-4171; Filed June 17, 2016, 5:22 p.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
BOARD OF AUDIOLOGY AND SPEECH-LANGUAGE PATHOLOGY
Final Regulation
Titles of Regulations: 18VAC30-20. Regulations Governing
the Practice of Audiology and Speech-Language Pathology (repealing 18VAC30-20-10 through
18VAC30-20-320).
18VAC30-21. Regulations Governing Audiology and
Speech-Language Pathology (adding 18VAC30-21-10 through 18VAC30-21-170).
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Effective Date: August 10, 2016.
Agency Contact: Leslie L. Knachel, Executive Director,
Board of Audiology and Speech-Language Pathology, 9960 Mayland Drive, Suite
300, Richmond, VA 23233-1463, telephone (804) 367-4630, FAX (804) 527-4413, or
email leslie.knachel@dhp.virginia.gov.
Summary:
The action repeals 18VAC30-20 and adopts new regulations in
18VAC30-21 to organize sections and provisions more logically and with more
clarity. Provisions of the regulation include (i) a change in continuing
competency requirements from 30 hours within two years to 10 hours annually,
offered by an approved sponsor or provider; (ii) less burdensome rules for
licensure and reentry into practice; (iii) elimination of barriers to
provisional licensure, including requirements pursuant to Chapter 436 of the
2013 Acts of Assembly; (iv) more explicit rules for patient confidentiality and
maintenance of records and regarding violations of professional boundaries; and
(v) performance of flexible endoscopic evaluation of swallowing.
Summary of Public Comments and Agency's Response: No
public comments were received by the promulgating agency.
CHAPTER 21
REGULATIONS GOVERNING AUDIOLOGY AND SPEECH-LANGUAGE PATHOLOGY
Part I
General Provisions
18VAC30-21-10. Definitions.
A. The words and terms "audiologist,"
"board," "practice of audiology," "practice of
speech-language pathology," "speech-language disorders," and
"speech-language pathologist" when used in this chapter shall have
the meanings ascribed to them in § 54.1-2600 of the Code of Virginia.
B. The following words and terms when used in this chapter
shall have the following meanings unless the context clearly indicates
otherwise:
"Active practice" means a minimum of 160 hours
of professional practice as an audiologist or speech-language pathologist for
each 12-month period immediately preceding application for licensure. Active
practice may include supervisory, administrative, educational, research, or
consultative activities or responsibilities for the delivery of such services.
"ASHA" means the American
Speech-Language-Hearing Association.
"Client" means a patient or person receiving
services in audiology or speech-language pathology.
"Contact hour" means 60 minutes of time spent in
continuing learning activities.
"School speech-language pathologist" means a
person licensed pursuant to § 54.1-2603 of the Code of Virginia to provide
speech-language pathology services solely in public school divisions.
"Supervision" means that the audiologist or
speech-language pathologist is responsible for the entire service being
rendered or activity being performed, is available for consultation, and is
providing regular monitoring and documentation of clinical activities and
competencies of the person being supervised.
18VAC30-21-20. Required licenses; posting of licenses.
A. There shall be separate licenses for the practices of
audiology and speech-language pathology. It is prohibited for any person to
practice as an audiologist or a speech-language pathologist unless the person
has been issued the appropriate license.
B. A licensee shall post his license in a place
conspicuous to the public in each facility in which the licensee is employed
and holds himself out to practice. If it is not practical to post the license,
the licensee shall provide a copy of his license upon request.
18VAC30-21-30. Records; accuracy of information.
A. All changes of name, address of record, or public
address, if different from the address of record, shall be furnished to the
board within 30 days after the change occurs.
B. A licensee who has changed his name shall submit as
legal proof to the board a copy of the marriage certificate, a certificate of
naturalization, or a court order evidencing the change. A duplicate license
with the changed name shall be issued by the board upon receipt of such
evidence and the required fee.
C. All notices required by law and by this chapter to be
mailed by the board to any registrant or licensee shall be validly served when
mailed to the latest address of record on file with the board.
18VAC30-21-40. Fees required.
A. The following fees shall be paid as applicable for
licensure:
1. Application for audiology or speech-language pathology
license
|
$135
|
2. Application for school speech-language pathology license
|
$70
|
3. Verification of licensure requests from other states
|
$20
|
4. Annual renewal of audiology or speech-language pathology
license
|
$75
|
5. Late renewal of audiology or speech-language pathology
license
|
$25
|
6. Annual renewal of school speech-language pathology
license
|
$40
|
7. Late renewal of school speech-language pathology license
|
$15
|
8. Reinstatement of audiology or speech-language pathology
license
|
$135
|
9. Reinstatement of school speech-language pathology
license
|
$70
|
10. Duplicate wall certificate
|
$25
|
11. Duplicate license
|
$5
|
12. Returned check
|
$35
|
13. Inactive license renewal for audiology or
speech-language pathology
|
$40
|
14. Inactive license renewal for school speech-language
pathology
|
$20
|
15. Application for provisional license
|
$50
|
16. Renewal of provisional license
|
$25
|
B. Fees shall be made payable to the Treasurer of Virginia
and shall not be refunded once submitted.
Part II
Requirements for Licensure
18VAC30-21-50. Application requirements.
A. A person seeking a provisional license or licensure as
an audiologist, a speech-language pathologist, or a school speech-language
pathologist shall submit:
1. A completed and signed application;
2. The applicable fee prescribed in 18VAC30-21-40;
3. Documentation as required by the board to determine if
the applicant has met the qualifications for licensure;
4. An attestation that the applicant has read, understands,
and will comply with the statutes and regulations governing the practice of
audiology or speech-language pathology; and
5. If licensed or certified in another United States
jurisdiction, verification of the status of the license or certification from
each jurisdiction in which licensure or certification is held.
B. An incomplete application package shall be retained by
the board for a period of one year from the date the application is received by
the board. If an application is not completed within the year, an applicant
shall reapply and pay a new application fee.
18VAC30-21-60. Qualifications for initial licensure.
A. The board may grant an initial license to an applicant
for licensure in audiology or speech-language pathology who:
1. Holds a current and unrestricted Certificate of Clinical
Competence issued by ASHA or certification issued by the American Board of Audiology
or any other accrediting body recognized by the board. Verification of currency
shall be in the form of a certified letter from a recognized accrediting body
issued within six months prior to filing an application for licensure; and
2. Has passed the qualifying examination from an
accrediting body recognized by the board.
B. The board may grant a license to an applicant as a
school speech-language pathologist who [ : 1. Holds
holds ] a master's degree in speech-language-pathology [ ;
and
2. Holds an endorsement in speech-language pathology
from the Virginia Department of Education.
C. Any individual who holds an active, renewable license
issued by the Virginia Board of Education with a valid endorsement in
speech-language pathology on June 30, 2014, shall be deemed qualified to obtain
a school speech-language pathologist license from the board until July 1, 2016,
or the date of expiration of such person's license issued by the Virginia Board
of Education, whichever is later. ]
18VAC30-21-70. Provisional licensure.
A. Provisional license to qualify for initial licensure.
An applicant may be issued a provisional license in order to obtain clinical
experience required for certification by ASHA, the American Board of Audiology,
or any other accrediting body recognized by the board. To obtain a
provisional license in order to qualify for initial licensure, the applicant
shall submit documentation that he has:
1. Passed the qualifying examination from an accrediting
body recognized by the board; and
2. Either:
a. For provisional licensure in audiology, successfully
completed all the didactic coursework required for the doctoral degree as
documented by a college or university whose audiology program is accredited by
the Council on Academic Accreditation of ASHA or an equivalent accrediting
body; or
b. For provisional licensure in speech-language pathology,
successfully completed all the didactic coursework required for a graduate
program in speech-language pathology as documented by a college or university
whose program is accredited by the Council on Academic Accreditation of the
American Speech-Language-Hearing Association or an equivalent accrediting body.
B. Provisional license to qualify for endorsement or
reentry into practice. An applicant may be issued a provisional license in
order to qualify for licensure by endorsement pursuant to 18VAC30-21-80,
reactivation of an inactive license pursuant to subsection C of 18VAC30-21-110,
or reinstatement of a lapsed license pursuant to subsection B of 18VAC30-21-120.
C. All provisional licenses shall expire 18 months from
the date of issuance and may be renewed for an additional six months by
submission of a renewal form and payment of a renewal fee. Renewal of a
provisional license beyond 24 months shall be for good cause shown as
determined by a committee of the board.
D. The holder of a provisional license in audiology shall
only practice under the supervision of a licensed audiologist, and the holder
of a provisional license in speech-language pathology shall only practice under
the supervision of a licensed speech-language pathologist. The provisional
licensee shall be responsible and accountable for the safe performance of those
direct client care tasks to which he has been assigned.
E. Licensed audiologists or speech-language pathologists
providing supervision shall:
1. Notify the board electronically or in writing of the
intent to provide supervision for a provisional licensee;
2. Have an active, current license and at least three years
of active practice as an audiologist or speech-language pathologist prior to
providing supervision;
3. Document the frequency and nature of the supervision of
provisional licensees;
4. Be responsible and accountable for the assignment of
clients and tasks based on their assessment and evaluation of the provisional
licensee's knowledge and skills; and
5. Monitor clinical performance and intervene if necessary
for the safety and protection of the clients.
F. The identity of a provisional licensee shall be
disclosed to the client prior to treatment and shall be made a part of the
client's file.
18VAC30-21-80. Qualifications for licensure by endorsement.
An applicant for licensure in audiology or speech-language
pathology who has been licensed in another United States jurisdiction may apply
for licensure in Virginia in accordance with application requirements in
18VAC30-20-50 and submission of documentation of:
1. Ten continuing education hours for each year in which he
has been licensed in the other jurisdiction, not to exceed 30 hours, or a
current and unrestricted Certificate of Clinical Competence in the area in
which he seeks licensure issued by ASHA or certification issued by the American
Board of Audiology or any other accrediting body recognized by the board.
Verification of currency shall be in the form of a certified letter from a
recognized accrediting body issued within six months prior to filing an
application for licensure;
2. Passage of the qualifying examination from an
accrediting body recognized by the board;
3. Current status of licensure in another United States
jurisdiction showing that no disciplinary action is pending or unresolved. The
board may deny a request for licensure to any applicant who has been determined
to have committed an act in violation of 18VAC30-21-160; and
4. Evidence of active practice in another United States
jurisdiction for at least one of the past three years or practice for six
months with a provisional license in accordance with 18VAC30-21-70 and by
providing evidence of a recommendation for licensure by his supervisor.
Part III
Renewal and Continuing Education
18VAC30-21-90. Renewal requirements.
A. A person who desires to renew his license shall, not
later than December 31 of each year, submit the renewal notice and applicable
renewal fee. A licensee who fails to renew his license by the expiration date
shall have a lapsed license, and practice with a lapsed license may constitute
grounds for disciplinary action by the board.
B. A person who fails to renew his license by the
expiration date may renew at any time within one year of expiration by
submission of a renewal notice, the renewal fee and late fee, and statement of
compliance with continuing education requirements.
18VAC30-21-100. Continuing education requirements for
renewal of an active license.
A. In order to renew an active license, a licensee shall
complete at least 10 contact hours of continuing education prior to December 31
of each year. Up to 10 contact hours of continuing education in excess of the
number required for renewal may be transferred or credited to the next renewal
year.
B. Continuing education shall be activities, programs, or
courses related to audiology or speech-language pathology, depending on the
license held, and offered or approved by one of the following accredited
sponsors or organizations sanctioned by the profession:
1. The Speech-Language-Hearing Association of Virginia or a
similar state speech-language-hearing association of another state;
2. The American Academy of Audiology;
3. The American Speech-Language-Hearing Association;
4. The Accreditation Council on Continuing Medical
Education of the American Medical Association offering Category I continuing
medical education;
5. Local, state, or federal government agencies;
6. Colleges and universities;
7. International Association of Continuing Education and
Training; or
8. Health care organizations accredited by the Joint
Commission on Accreditation of Healthcare Organizations.
C. If the licensee is dually licensed by this board as an
audiologist and speech-language pathologist, a total of no more than 15 hours
of continuing education are required for renewal of both licenses with a
minimum of 7.5 contact hours in each profession.
D. A licensee shall be exempt from the continuing
education requirements for the first renewal following the date of initial
licensure in Virginia under 18VAC30-20-60.
E. The licensee shall retain all continuing education
documentation for a period of three years following the renewal of an active
license. Documentation from the sponsor or organization shall include the title
of the course, the name of the sponsoring organization, the date of the course,
and the number of hours credited.
F. The board may grant an extension of the deadline for
continuing education requirements, for up to one year, for good cause shown
upon a written request from the licensee prior to the renewal date of December
[ 31st 31 ].
G. The board may grant an exemption for all or part of the
requirements for circumstances beyond the control of the licensee, such as
temporary disability, mandatory military service, or officially declared
disasters.
H. The board shall periodically conduct an audit for
compliance with continuing education requirements. Licensees selected for an
audit conducted by the board shall complete the Continuing Education Activity
and Assessment Form and provide all supporting documentation within 30 days of
receiving notification of the audit.
I. Failure to comply with these requirements may subject
the licensee to disciplinary action by the board.
Part IV
Reactivation and Reinstatement
18VAC30-21-110. Inactive licensure; reactivation for
audiologists [ and or ] speech-language
pathologists.
A. An audiologist or speech-language pathologist who holds
a current, unrestricted license in Virginia may, upon a request on the renewal
application and submission of the required fee, be issued an inactive license.
The holder of an inactive license shall not be required to maintain continuing
education requirements and shall not be entitled to perform any act requiring a
license to practice audiology or speech-language pathology in Virginia.
B. A licensee whose license has been inactive and who
requests reactivation of an active license shall file an application, pay the difference
between the inactive and active renewal fees for the current year, and provide
documentation of current ASHA certification or of having completed 10
continuing education hours equal to the requirement for the number of years in
which the license has been inactive, not to exceed 30 contact hours.
C. A licensee who does not reactivate within five years
shall meet the requirements of subsection B of this section and shall either:
1. Meet the requirements for initial licensure as
prescribed by 18VAC30-21-60; or
2. Provide documentation of a current license in another
jurisdiction in the United States and evidence of active practice for at least
one of the past three years or practice in accordance with 18VAC30-21-70
with a provisional license for six months and submit a recommendation for
licensure from his supervisor.
D. If the licensee holds licensure in any other state or
jurisdiction, he shall provide evidence that no disciplinary action is pending
or unresolved. The board may deny a request for reactivation to any licensee
who has been determined to have committed an act in violation of
18VAC30-21-160.
18VAC30-21-120. Reinstatement of a lapsed license for
audiologists or speech-language pathologists.
A. When a license has not been renewed within one year of
the expiration date, a person may apply to reinstate his license by submission
of a reinstatement application, payment of the reinstatement fee, and
submission of documentation of current ASHA certification or at least 10
continuing education hours for each year the license has been lapsed, not to
exceed 30 contact hours, obtained during the time the license in Virginia was
lapsed.
B. A licensee who does not reinstate within five years
shall meet the requirements of subsection A of this section and shall either:
1. Reinstate by meeting the requirements for initial
licensure as prescribed by 18VAC30-21-60; or
2. Provide documentation of a current license in another
United States jurisdiction and evidence of active practice for at least one of
the past three years or practice in accordance with 18VAC30-21-70 with a
provisional license for six months and submit a recommendation for licensure
from his supervisor.
C. If the licensee holds licensure in any other state or
jurisdiction, he shall provide evidence that no disciplinary action is pending
or unresolved. The board may deny a request for reinstatement to any licensee
who has been determined to have committed an act in violation of
18VAC30-21-160.
18VAC30-21-130. Reactivation or reinstatement of a school
speech-language pathologist.
A. A school speech-language pathologist whose license has
been inactive and who requests reactivation of an active license shall file an
application and pay the difference between the inactive and active renewal fees
for the current year. A school speech-language pathologist whose license
has lapsed and who requests reinstatement shall file an application and pay the
reinstatement fee as set forth in 18VAC30-20-40.
B. The board may reactivate or reinstate licensure as a
school speech-language pathologist to an applicant who:
1. Holds a master's degree in speech-language-pathology;
and
2. Holds a current endorsement in speech-language pathology
from the Virginia Department of Education.
C. The board may deny a request for reactivation or
reinstatement to any licensee who has been determined to have committed an act
in violation of 18VAC30-21-160.
[ 18VAC30-21-131. Performance of flexible endoscopic
evaluation of swallowing.
A. For the purposes of this section, an endoscopic
procedure shall mean a flexible endoscopic evaluation of swallowing limited to
the use of flexible endoscopes to observe, collect data, and measure the
parameters of swallowing for the purposes of functional assessment and therapy
planning.
B. A speech-language pathologist who performs an
endoscopic procedure shall meet the following qualifications:
1. Completion of a course or courses or an educational
program offered by a provider approved in 18VAC30-20-100 that includes at least
12 hours on endoscopic procedures;
2. Successful performance of at least 25 flexible
endoscopic procedures under the immediate and direct supervision of a
board-certified otolaryngologist or another speech-language pathologist who has
successfully performed at least 50 flexible endoscopic procedures beyond the 25
required for initial qualification and has been approved in writing by a
board-certified otolaryngologist to provide that supervision; and
3. Current certification in basic life support.
C. The speech-language pathologist who qualifies to
perform an endoscopic procedure pursuant to subsection B of this section shall
maintain documentation of course completion and written verification from the
supervising otolaryngologist or speech-language pathologist of successful
completion of flexible endoscopic procedures.
D. An endoscopic procedure shall only be performed by a
speech-language pathologist on referral from an otolaryngologist or other qualified
physician.
E. A speech-language pathologist shall only perform an
endoscopic procedure in a facility that has protocols in place for emergency
medical backup. A flexible endoscopic evaluation of swallowing shall only be
performed by a speech-language pathologist in either:
1. A licensed hospital or nursing home under the general
supervision of a physician who is readily available in the event of an
emergency, including physical presence in the facility or available by
telephone; or
2. A physician's office at which the physician is on
premises and available to provide onsite supervision.
F. The speech-language pathologist shall promptly report
any observed abnormality or adverse reaction to the referring physician, an
appropriate medical specialist, or both. The speech-language pathologist shall
provide a report of an endoscopic procedure to the referring physician in a
timely manner and, if requested, shall ensure access to a visual recording for
viewing.
G. A speech-language pathologist is not authorized to
possess or administer prescription drugs except as provided in § 54.1-3408 B of
the Code of Virginia.
H. A speech-language pathologist who has been performing
flexible endoscopic evaluations of swallowing prior to October 7, 2015, may
continue to perform such evaluations provided he has written verification from
a board-certified otolaryngologist that he has the appropriate training,
knowledge, and skills to safely perform such evaluations. ]
Part V
Standards of Practice
18VAC30-21-140. Supervision of unlicensed assistants.
A. If a licensed audiologist or speech-language
pathologist has unlicensed assistants, he shall document supervision of them,
shall be held fully responsible for their performance and activities, and shall
ensure that they perform only those activities which do not constitute the
practice of audiology or speech-language pathology and which are commensurate
with their level of training.
B. A licensee may delegate to an unlicensed assistant such
activities or functions that are nondiscretionary and do not require the
exercise of professional judgment for performance.
C. The identity of the unlicensed assistant shall be
disclosed to the client prior to treatment and shall be made a part of the
client's file.
18VAC30-21-150. Prohibited conduct.
A. No person, unless otherwise licensed to do so, shall
prepare, order, dispense, alter, or repair hearing aids or parts of or
attachments to hearing aids for consideration. However, audiologists licensed
under this chapter may make earmold impressions and prepare and alter earmolds
for clinical use and research.
B. No person licensed as a school speech-language
pathologist shall conduct the practice of speech-language pathology outside of
the public school setting.
18VAC30-21-160. Unprofessional conduct.
The board may refuse to issue a license to any applicant,
suspend a license for a stated period of time or indefinitely, reprimand a
licensee or place his license on probation with such terms and conditions and
for such time as it may designate, impose a monetary penalty, or revoke a
license for any of the following:
1. Guarantee of the results of any speech, voice, language,
or hearing consultative or therapeutic procedure or exploitation of clients by
accepting them for treatment when benefit cannot reasonably be expected to
occur or by continuing treatment unnecessarily;
2. Diagnosis or treatment of speech, voice, language, and
hearing disorders solely by written correspondence, provided this shall not
preclude:
a. Follow-up by written correspondence or electronic
communication concerning individuals previously seen; or
b. Providing clients with general information of an
educational nature;
3. Failure to comply with provisions of
§ 32.1-127.1:03 of the Code of Virginia related to the confidentiality and
disclosure of client records or related to provision of client records to
another practitioner or to the client or his personal representative;
4. Failure to properly manage and keep timely, accurate,
legible, and complete client records, to include the following:
a. For licensees who are employed by a health care
institution, school system, or other entity, in which the individual
practitioner does not own or maintain his own records, failure to maintain
client records in accordance with the policies and procedures of the employing
entity; or
b. For licensees who are self-employed or employed by an
entity in which the individual practitioner does own and is responsible for
client records, failure to maintain a client record for a minimum of six years
following the last client encounter with the following exceptions:
(1) For records of a minor child, the minimum time is six
years from the last client encounter or until the child reaches the age of 18
or becomes emancipated, whichever is longer; or
(2) Records that have previously been transferred to
another practitioner or health care provider or provided to the client or his
personal representative as documented in a record or database maintained for a
minimum of six years;
5. Engaging or attempting to engage in a relationship with
a client that constitutes a professional boundary violation in which the
practitioner uses his professional position to take advantage of the
vulnerability of a client or a client's family, including but not limited to
sexual misconduct with a client or a member of the client's family or other
conduct that results or could result in personal gain at the expense of the
client;
6. Incompetence or negligence in the practice of the
profession;
7. Failure to comply with applicable state and federal
statutes or regulations specifying the consultations and examinations required
prior to the fitting of a new or replacement prosthetic aid for any
communicatively impaired person;
8. Failure to refer a client to an appropriate health care
practitioner when there is evidence of an impairment for which assessment,
evaluation, care, or treatment might be necessary;
9. Failure to supervise persons who assist in the practice
of audiology or speech-language pathology as well as failure to disclose the
use and identity of unlicensed assistants;
10. Conviction of a felony or a misdemeanor involving moral
turpitude;
11. Violating or cooperating with others in violating any
of the provisions of Chapters 1 (§ 54.1-100 et seq.), 24 (§ 54.1-2400
et seq.), or 26 (§ 54.1-2600 et seq.) of Title 54 of the Code of Virginia or
the regulations of the board;
12. Publishing or causing to be published in any manner an
advertisement relating to his professional practice that is false, deceptive,
or misleading;
13. Inability to practice with skill and safety;
14. Fraud, deceit, or misrepresentation in provision of
documentation or information to the board or in the practice of audiology or
speech-language pathology;
15. Aiding and abetting unlicensed activity; or
16. Revocation, suspension, restriction, or any other
discipline of a license or certificate to practice or surrender of license or
certificate while an investigation or administrative proceedings are pending in
another regulatory agency in Virginia or another jurisdiction.
18VAC30-21-170. Criteria for delegation to an agency
subordinate.
A. Decision to delegate. In accordance with subdivision 10
of § 54.1-2400 of the Code of Virginia, the board may delegate an informal
fact-finding proceeding to an agency subordinate upon determination that
probable cause exists that a practitioner may be subject to a disciplinary
action.
B. Criteria for delegation. Cases that may not be
delegated to an agency subordinate are those that involve:
1. Intentional or negligent conduct that causes or is
likely to cause injury to a patient;
2. Mandatory suspension resulting from action by another jurisdiction
or a felony conviction;
3. Impairment with an inability to practice with skill and
safety;
4. Sexual misconduct;
5. Unauthorized practice.
C. Criteria for an agency subordinate.
1. An agency subordinate authorized by the board to conduct
an informal fact-finding proceeding may include board members and professional
staff or other persons deemed knowledgeable by virtue of their training and
experience in administrative proceedings involving the regulation and
discipline of health professionals.
2. The executive director shall maintain a list of
appropriately qualified persons to whom an informal fact-finding proceeding may
be delegated.
3. The board may delegate to the executive director the
selection of the agency subordinate who is deemed appropriately qualified to
conduct a proceeding based on the qualifications of the subordinate and the
type of case being heard.
NOTICE: The following
forms used in administering the regulation were filed by the agency. The forms
are not being published; however, online users of this issue of the Virginia
Register of Regulations may click on the name of a form with a hyperlink to
access it. The forms are also available from the agency contact or may be
viewed at the Office of the Registrar of Regulations, General Assembly
Building, 2nd Floor, Richmond, Virginia 23219.
FORMS (18VAC30-21)
Continuing
Education Form (rev. 3/2015)
VA.R. Doc. No. R11-2759; Filed June 18, 2016, 11:21 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
BOARD OF AUDIOLOGY AND SPEECH-LANGUAGE PATHOLOGY
Final Regulation
Titles of Regulations: 18VAC30-20. Regulations Governing
the Practice of Audiology and Speech-Language Pathology (repealing 18VAC30-20-10 through
18VAC30-20-320).
18VAC30-21. Regulations Governing Audiology and
Speech-Language Pathology (adding 18VAC30-21-10 through 18VAC30-21-170).
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Effective Date: August 10, 2016.
Agency Contact: Leslie L. Knachel, Executive Director,
Board of Audiology and Speech-Language Pathology, 9960 Mayland Drive, Suite
300, Richmond, VA 23233-1463, telephone (804) 367-4630, FAX (804) 527-4413, or
email leslie.knachel@dhp.virginia.gov.
Summary:
The action repeals 18VAC30-20 and adopts new regulations in
18VAC30-21 to organize sections and provisions more logically and with more
clarity. Provisions of the regulation include (i) a change in continuing
competency requirements from 30 hours within two years to 10 hours annually,
offered by an approved sponsor or provider; (ii) less burdensome rules for
licensure and reentry into practice; (iii) elimination of barriers to
provisional licensure, including requirements pursuant to Chapter 436 of the
2013 Acts of Assembly; (iv) more explicit rules for patient confidentiality and
maintenance of records and regarding violations of professional boundaries; and
(v) performance of flexible endoscopic evaluation of swallowing.
Summary of Public Comments and Agency's Response: No
public comments were received by the promulgating agency.
CHAPTER 21
REGULATIONS GOVERNING AUDIOLOGY AND SPEECH-LANGUAGE PATHOLOGY
Part I
General Provisions
18VAC30-21-10. Definitions.
A. The words and terms "audiologist,"
"board," "practice of audiology," "practice of
speech-language pathology," "speech-language disorders," and
"speech-language pathologist" when used in this chapter shall have
the meanings ascribed to them in § 54.1-2600 of the Code of Virginia.
B. The following words and terms when used in this chapter
shall have the following meanings unless the context clearly indicates
otherwise:
"Active practice" means a minimum of 160 hours
of professional practice as an audiologist or speech-language pathologist for
each 12-month period immediately preceding application for licensure. Active
practice may include supervisory, administrative, educational, research, or
consultative activities or responsibilities for the delivery of such services.
"ASHA" means the American
Speech-Language-Hearing Association.
"Client" means a patient or person receiving
services in audiology or speech-language pathology.
"Contact hour" means 60 minutes of time spent in
continuing learning activities.
"School speech-language pathologist" means a
person licensed pursuant to § 54.1-2603 of the Code of Virginia to provide
speech-language pathology services solely in public school divisions.
"Supervision" means that the audiologist or
speech-language pathologist is responsible for the entire service being
rendered or activity being performed, is available for consultation, and is
providing regular monitoring and documentation of clinical activities and
competencies of the person being supervised.
18VAC30-21-20. Required licenses; posting of licenses.
A. There shall be separate licenses for the practices of
audiology and speech-language pathology. It is prohibited for any person to
practice as an audiologist or a speech-language pathologist unless the person
has been issued the appropriate license.
B. A licensee shall post his license in a place
conspicuous to the public in each facility in which the licensee is employed
and holds himself out to practice. If it is not practical to post the license,
the licensee shall provide a copy of his license upon request.
18VAC30-21-30. Records; accuracy of information.
A. All changes of name, address of record, or public
address, if different from the address of record, shall be furnished to the
board within 30 days after the change occurs.
B. A licensee who has changed his name shall submit as
legal proof to the board a copy of the marriage certificate, a certificate of
naturalization, or a court order evidencing the change. A duplicate license
with the changed name shall be issued by the board upon receipt of such
evidence and the required fee.
C. All notices required by law and by this chapter to be
mailed by the board to any registrant or licensee shall be validly served when
mailed to the latest address of record on file with the board.
18VAC30-21-40. Fees required.
A. The following fees shall be paid as applicable for
licensure:
1. Application for audiology or speech-language pathology
license
|
$135
|
2. Application for school speech-language pathology license
|
$70
|
3. Verification of licensure requests from other states
|
$20
|
4. Annual renewal of audiology or speech-language pathology
license
|
$75
|
5. Late renewal of audiology or speech-language pathology
license
|
$25
|
6. Annual renewal of school speech-language pathology
license
|
$40
|
7. Late renewal of school speech-language pathology license
|
$15
|
8. Reinstatement of audiology or speech-language pathology
license
|
$135
|
9. Reinstatement of school speech-language pathology
license
|
$70
|
10. Duplicate wall certificate
|
$25
|
11. Duplicate license
|
$5
|
12. Returned check
|
$35
|
13. Inactive license renewal for audiology or
speech-language pathology
|
$40
|
14. Inactive license renewal for school speech-language
pathology
|
$20
|
15. Application for provisional license
|
$50
|
16. Renewal of provisional license
|
$25
|
B. Fees shall be made payable to the Treasurer of Virginia
and shall not be refunded once submitted.
Part II
Requirements for Licensure
18VAC30-21-50. Application requirements.
A. A person seeking a provisional license or licensure as
an audiologist, a speech-language pathologist, or a school speech-language
pathologist shall submit:
1. A completed and signed application;
2. The applicable fee prescribed in 18VAC30-21-40;
3. Documentation as required by the board to determine if
the applicant has met the qualifications for licensure;
4. An attestation that the applicant has read, understands,
and will comply with the statutes and regulations governing the practice of
audiology or speech-language pathology; and
5. If licensed or certified in another United States
jurisdiction, verification of the status of the license or certification from
each jurisdiction in which licensure or certification is held.
B. An incomplete application package shall be retained by
the board for a period of one year from the date the application is received by
the board. If an application is not completed within the year, an applicant
shall reapply and pay a new application fee.
18VAC30-21-60. Qualifications for initial licensure.
A. The board may grant an initial license to an applicant
for licensure in audiology or speech-language pathology who:
1. Holds a current and unrestricted Certificate of Clinical
Competence issued by ASHA or certification issued by the American Board of Audiology
or any other accrediting body recognized by the board. Verification of currency
shall be in the form of a certified letter from a recognized accrediting body
issued within six months prior to filing an application for licensure; and
2. Has passed the qualifying examination from an
accrediting body recognized by the board.
B. The board may grant a license to an applicant as a
school speech-language pathologist who [ : 1. Holds
holds ] a master's degree in speech-language-pathology [ ;
and
2. Holds an endorsement in speech-language pathology
from the Virginia Department of Education.
C. Any individual who holds an active, renewable license
issued by the Virginia Board of Education with a valid endorsement in
speech-language pathology on June 30, 2014, shall be deemed qualified to obtain
a school speech-language pathologist license from the board until July 1, 2016,
or the date of expiration of such person's license issued by the Virginia Board
of Education, whichever is later. ]
18VAC30-21-70. Provisional licensure.
A. Provisional license to qualify for initial licensure.
An applicant may be issued a provisional license in order to obtain clinical
experience required for certification by ASHA, the American Board of Audiology,
or any other accrediting body recognized by the board. To obtain a
provisional license in order to qualify for initial licensure, the applicant
shall submit documentation that he has:
1. Passed the qualifying examination from an accrediting
body recognized by the board; and
2. Either:
a. For provisional licensure in audiology, successfully
completed all the didactic coursework required for the doctoral degree as
documented by a college or university whose audiology program is accredited by
the Council on Academic Accreditation of ASHA or an equivalent accrediting
body; or
b. For provisional licensure in speech-language pathology,
successfully completed all the didactic coursework required for a graduate
program in speech-language pathology as documented by a college or university
whose program is accredited by the Council on Academic Accreditation of the
American Speech-Language-Hearing Association or an equivalent accrediting body.
B. Provisional license to qualify for endorsement or
reentry into practice. An applicant may be issued a provisional license in
order to qualify for licensure by endorsement pursuant to 18VAC30-21-80,
reactivation of an inactive license pursuant to subsection C of 18VAC30-21-110,
or reinstatement of a lapsed license pursuant to subsection B of 18VAC30-21-120.
C. All provisional licenses shall expire 18 months from
the date of issuance and may be renewed for an additional six months by
submission of a renewal form and payment of a renewal fee. Renewal of a
provisional license beyond 24 months shall be for good cause shown as
determined by a committee of the board.
D. The holder of a provisional license in audiology shall
only practice under the supervision of a licensed audiologist, and the holder
of a provisional license in speech-language pathology shall only practice under
the supervision of a licensed speech-language pathologist. The provisional
licensee shall be responsible and accountable for the safe performance of those
direct client care tasks to which he has been assigned.
E. Licensed audiologists or speech-language pathologists
providing supervision shall:
1. Notify the board electronically or in writing of the
intent to provide supervision for a provisional licensee;
2. Have an active, current license and at least three years
of active practice as an audiologist or speech-language pathologist prior to
providing supervision;
3. Document the frequency and nature of the supervision of
provisional licensees;
4. Be responsible and accountable for the assignment of
clients and tasks based on their assessment and evaluation of the provisional
licensee's knowledge and skills; and
5. Monitor clinical performance and intervene if necessary
for the safety and protection of the clients.
F. The identity of a provisional licensee shall be
disclosed to the client prior to treatment and shall be made a part of the
client's file.
18VAC30-21-80. Qualifications for licensure by endorsement.
An applicant for licensure in audiology or speech-language
pathology who has been licensed in another United States jurisdiction may apply
for licensure in Virginia in accordance with application requirements in
18VAC30-20-50 and submission of documentation of:
1. Ten continuing education hours for each year in which he
has been licensed in the other jurisdiction, not to exceed 30 hours, or a
current and unrestricted Certificate of Clinical Competence in the area in
which he seeks licensure issued by ASHA or certification issued by the American
Board of Audiology or any other accrediting body recognized by the board.
Verification of currency shall be in the form of a certified letter from a
recognized accrediting body issued within six months prior to filing an
application for licensure;
2. Passage of the qualifying examination from an
accrediting body recognized by the board;
3. Current status of licensure in another United States
jurisdiction showing that no disciplinary action is pending or unresolved. The
board may deny a request for licensure to any applicant who has been determined
to have committed an act in violation of 18VAC30-21-160; and
4. Evidence of active practice in another United States
jurisdiction for at least one of the past three years or practice for six
months with a provisional license in accordance with 18VAC30-21-70 and by
providing evidence of a recommendation for licensure by his supervisor.
Part III
Renewal and Continuing Education
18VAC30-21-90. Renewal requirements.
A. A person who desires to renew his license shall, not
later than December 31 of each year, submit the renewal notice and applicable
renewal fee. A licensee who fails to renew his license by the expiration date
shall have a lapsed license, and practice with a lapsed license may constitute
grounds for disciplinary action by the board.
B. A person who fails to renew his license by the
expiration date may renew at any time within one year of expiration by
submission of a renewal notice, the renewal fee and late fee, and statement of
compliance with continuing education requirements.
18VAC30-21-100. Continuing education requirements for
renewal of an active license.
A. In order to renew an active license, a licensee shall
complete at least 10 contact hours of continuing education prior to December 31
of each year. Up to 10 contact hours of continuing education in excess of the
number required for renewal may be transferred or credited to the next renewal
year.
B. Continuing education shall be activities, programs, or
courses related to audiology or speech-language pathology, depending on the
license held, and offered or approved by one of the following accredited
sponsors or organizations sanctioned by the profession:
1. The Speech-Language-Hearing Association of Virginia or a
similar state speech-language-hearing association of another state;
2. The American Academy of Audiology;
3. The American Speech-Language-Hearing Association;
4. The Accreditation Council on Continuing Medical
Education of the American Medical Association offering Category I continuing
medical education;
5. Local, state, or federal government agencies;
6. Colleges and universities;
7. International Association of Continuing Education and
Training; or
8. Health care organizations accredited by the Joint
Commission on Accreditation of Healthcare Organizations.
C. If the licensee is dually licensed by this board as an
audiologist and speech-language pathologist, a total of no more than 15 hours
of continuing education are required for renewal of both licenses with a
minimum of 7.5 contact hours in each profession.
D. A licensee shall be exempt from the continuing
education requirements for the first renewal following the date of initial
licensure in Virginia under 18VAC30-20-60.
E. The licensee shall retain all continuing education
documentation for a period of three years following the renewal of an active
license. Documentation from the sponsor or organization shall include the title
of the course, the name of the sponsoring organization, the date of the course,
and the number of hours credited.
F. The board may grant an extension of the deadline for
continuing education requirements, for up to one year, for good cause shown
upon a written request from the licensee prior to the renewal date of December
[ 31st 31 ].
G. The board may grant an exemption for all or part of the
requirements for circumstances beyond the control of the licensee, such as
temporary disability, mandatory military service, or officially declared
disasters.
H. The board shall periodically conduct an audit for
compliance with continuing education requirements. Licensees selected for an
audit conducted by the board shall complete the Continuing Education Activity
and Assessment Form and provide all supporting documentation within 30 days of
receiving notification of the audit.
I. Failure to comply with these requirements may subject
the licensee to disciplinary action by the board.
Part IV
Reactivation and Reinstatement
18VAC30-21-110. Inactive licensure; reactivation for
audiologists [ and or ] speech-language
pathologists.
A. An audiologist or speech-language pathologist who holds
a current, unrestricted license in Virginia may, upon a request on the renewal
application and submission of the required fee, be issued an inactive license.
The holder of an inactive license shall not be required to maintain continuing
education requirements and shall not be entitled to perform any act requiring a
license to practice audiology or speech-language pathology in Virginia.
B. A licensee whose license has been inactive and who
requests reactivation of an active license shall file an application, pay the difference
between the inactive and active renewal fees for the current year, and provide
documentation of current ASHA certification or of having completed 10
continuing education hours equal to the requirement for the number of years in
which the license has been inactive, not to exceed 30 contact hours.
C. A licensee who does not reactivate within five years
shall meet the requirements of subsection B of this section and shall either:
1. Meet the requirements for initial licensure as
prescribed by 18VAC30-21-60; or
2. Provide documentation of a current license in another
jurisdiction in the United States and evidence of active practice for at least
one of the past three years or practice in accordance with 18VAC30-21-70
with a provisional license for six months and submit a recommendation for
licensure from his supervisor.
D. If the licensee holds licensure in any other state or
jurisdiction, he shall provide evidence that no disciplinary action is pending
or unresolved. The board may deny a request for reactivation to any licensee
who has been determined to have committed an act in violation of
18VAC30-21-160.
18VAC30-21-120. Reinstatement of a lapsed license for
audiologists or speech-language pathologists.
A. When a license has not been renewed within one year of
the expiration date, a person may apply to reinstate his license by submission
of a reinstatement application, payment of the reinstatement fee, and
submission of documentation of current ASHA certification or at least 10
continuing education hours for each year the license has been lapsed, not to
exceed 30 contact hours, obtained during the time the license in Virginia was
lapsed.
B. A licensee who does not reinstate within five years
shall meet the requirements of subsection A of this section and shall either:
1. Reinstate by meeting the requirements for initial
licensure as prescribed by 18VAC30-21-60; or
2. Provide documentation of a current license in another
United States jurisdiction and evidence of active practice for at least one of
the past three years or practice in accordance with 18VAC30-21-70 with a
provisional license for six months and submit a recommendation for licensure
from his supervisor.
C. If the licensee holds licensure in any other state or
jurisdiction, he shall provide evidence that no disciplinary action is pending
or unresolved. The board may deny a request for reinstatement to any licensee
who has been determined to have committed an act in violation of
18VAC30-21-160.
18VAC30-21-130. Reactivation or reinstatement of a school
speech-language pathologist.
A. A school speech-language pathologist whose license has
been inactive and who requests reactivation of an active license shall file an
application and pay the difference between the inactive and active renewal fees
for the current year. A school speech-language pathologist whose license
has lapsed and who requests reinstatement shall file an application and pay the
reinstatement fee as set forth in 18VAC30-20-40.
B. The board may reactivate or reinstate licensure as a
school speech-language pathologist to an applicant who:
1. Holds a master's degree in speech-language-pathology;
and
2. Holds a current endorsement in speech-language pathology
from the Virginia Department of Education.
C. The board may deny a request for reactivation or
reinstatement to any licensee who has been determined to have committed an act
in violation of 18VAC30-21-160.
[ 18VAC30-21-131. Performance of flexible endoscopic
evaluation of swallowing.
A. For the purposes of this section, an endoscopic
procedure shall mean a flexible endoscopic evaluation of swallowing limited to
the use of flexible endoscopes to observe, collect data, and measure the
parameters of swallowing for the purposes of functional assessment and therapy
planning.
B. A speech-language pathologist who performs an
endoscopic procedure shall meet the following qualifications:
1. Completion of a course or courses or an educational
program offered by a provider approved in 18VAC30-20-100 that includes at least
12 hours on endoscopic procedures;
2. Successful performance of at least 25 flexible
endoscopic procedures under the immediate and direct supervision of a
board-certified otolaryngologist or another speech-language pathologist who has
successfully performed at least 50 flexible endoscopic procedures beyond the 25
required for initial qualification and has been approved in writing by a
board-certified otolaryngologist to provide that supervision; and
3. Current certification in basic life support.
C. The speech-language pathologist who qualifies to
perform an endoscopic procedure pursuant to subsection B of this section shall
maintain documentation of course completion and written verification from the
supervising otolaryngologist or speech-language pathologist of successful
completion of flexible endoscopic procedures.
D. An endoscopic procedure shall only be performed by a
speech-language pathologist on referral from an otolaryngologist or other qualified
physician.
E. A speech-language pathologist shall only perform an
endoscopic procedure in a facility that has protocols in place for emergency
medical backup. A flexible endoscopic evaluation of swallowing shall only be
performed by a speech-language pathologist in either:
1. A licensed hospital or nursing home under the general
supervision of a physician who is readily available in the event of an
emergency, including physical presence in the facility or available by
telephone; or
2. A physician's office at which the physician is on
premises and available to provide onsite supervision.
F. The speech-language pathologist shall promptly report
any observed abnormality or adverse reaction to the referring physician, an
appropriate medical specialist, or both. The speech-language pathologist shall
provide a report of an endoscopic procedure to the referring physician in a
timely manner and, if requested, shall ensure access to a visual recording for
viewing.
G. A speech-language pathologist is not authorized to
possess or administer prescription drugs except as provided in § 54.1-3408 B of
the Code of Virginia.
H. A speech-language pathologist who has been performing
flexible endoscopic evaluations of swallowing prior to October 7, 2015, may
continue to perform such evaluations provided he has written verification from
a board-certified otolaryngologist that he has the appropriate training,
knowledge, and skills to safely perform such evaluations. ]
Part V
Standards of Practice
18VAC30-21-140. Supervision of unlicensed assistants.
A. If a licensed audiologist or speech-language
pathologist has unlicensed assistants, he shall document supervision of them,
shall be held fully responsible for their performance and activities, and shall
ensure that they perform only those activities which do not constitute the
practice of audiology or speech-language pathology and which are commensurate
with their level of training.
B. A licensee may delegate to an unlicensed assistant such
activities or functions that are nondiscretionary and do not require the
exercise of professional judgment for performance.
C. The identity of the unlicensed assistant shall be
disclosed to the client prior to treatment and shall be made a part of the
client's file.
18VAC30-21-150. Prohibited conduct.
A. No person, unless otherwise licensed to do so, shall
prepare, order, dispense, alter, or repair hearing aids or parts of or
attachments to hearing aids for consideration. However, audiologists licensed
under this chapter may make earmold impressions and prepare and alter earmolds
for clinical use and research.
B. No person licensed as a school speech-language
pathologist shall conduct the practice of speech-language pathology outside of
the public school setting.
18VAC30-21-160. Unprofessional conduct.
The board may refuse to issue a license to any applicant,
suspend a license for a stated period of time or indefinitely, reprimand a
licensee or place his license on probation with such terms and conditions and
for such time as it may designate, impose a monetary penalty, or revoke a
license for any of the following:
1. Guarantee of the results of any speech, voice, language,
or hearing consultative or therapeutic procedure or exploitation of clients by
accepting them for treatment when benefit cannot reasonably be expected to
occur or by continuing treatment unnecessarily;
2. Diagnosis or treatment of speech, voice, language, and
hearing disorders solely by written correspondence, provided this shall not
preclude:
a. Follow-up by written correspondence or electronic
communication concerning individuals previously seen; or
b. Providing clients with general information of an
educational nature;
3. Failure to comply with provisions of
§ 32.1-127.1:03 of the Code of Virginia related to the confidentiality and
disclosure of client records or related to provision of client records to
another practitioner or to the client or his personal representative;
4. Failure to properly manage and keep timely, accurate,
legible, and complete client records, to include the following:
a. For licensees who are employed by a health care
institution, school system, or other entity, in which the individual
practitioner does not own or maintain his own records, failure to maintain
client records in accordance with the policies and procedures of the employing
entity; or
b. For licensees who are self-employed or employed by an
entity in which the individual practitioner does own and is responsible for
client records, failure to maintain a client record for a minimum of six years
following the last client encounter with the following exceptions:
(1) For records of a minor child, the minimum time is six
years from the last client encounter or until the child reaches the age of 18
or becomes emancipated, whichever is longer; or
(2) Records that have previously been transferred to
another practitioner or health care provider or provided to the client or his
personal representative as documented in a record or database maintained for a
minimum of six years;
5. Engaging or attempting to engage in a relationship with
a client that constitutes a professional boundary violation in which the
practitioner uses his professional position to take advantage of the
vulnerability of a client or a client's family, including but not limited to
sexual misconduct with a client or a member of the client's family or other
conduct that results or could result in personal gain at the expense of the
client;
6. Incompetence or negligence in the practice of the
profession;
7. Failure to comply with applicable state and federal
statutes or regulations specifying the consultations and examinations required
prior to the fitting of a new or replacement prosthetic aid for any
communicatively impaired person;
8. Failure to refer a client to an appropriate health care
practitioner when there is evidence of an impairment for which assessment,
evaluation, care, or treatment might be necessary;
9. Failure to supervise persons who assist in the practice
of audiology or speech-language pathology as well as failure to disclose the
use and identity of unlicensed assistants;
10. Conviction of a felony or a misdemeanor involving moral
turpitude;
11. Violating or cooperating with others in violating any
of the provisions of Chapters 1 (§ 54.1-100 et seq.), 24 (§ 54.1-2400
et seq.), or 26 (§ 54.1-2600 et seq.) of Title 54 of the Code of Virginia or
the regulations of the board;
12. Publishing or causing to be published in any manner an
advertisement relating to his professional practice that is false, deceptive,
or misleading;
13. Inability to practice with skill and safety;
14. Fraud, deceit, or misrepresentation in provision of
documentation or information to the board or in the practice of audiology or
speech-language pathology;
15. Aiding and abetting unlicensed activity; or
16. Revocation, suspension, restriction, or any other
discipline of a license or certificate to practice or surrender of license or
certificate while an investigation or administrative proceedings are pending in
another regulatory agency in Virginia or another jurisdiction.
18VAC30-21-170. Criteria for delegation to an agency
subordinate.
A. Decision to delegate. In accordance with subdivision 10
of § 54.1-2400 of the Code of Virginia, the board may delegate an informal
fact-finding proceeding to an agency subordinate upon determination that
probable cause exists that a practitioner may be subject to a disciplinary
action.
B. Criteria for delegation. Cases that may not be
delegated to an agency subordinate are those that involve:
1. Intentional or negligent conduct that causes or is
likely to cause injury to a patient;
2. Mandatory suspension resulting from action by another jurisdiction
or a felony conviction;
3. Impairment with an inability to practice with skill and
safety;
4. Sexual misconduct;
5. Unauthorized practice.
C. Criteria for an agency subordinate.
1. An agency subordinate authorized by the board to conduct
an informal fact-finding proceeding may include board members and professional
staff or other persons deemed knowledgeable by virtue of their training and
experience in administrative proceedings involving the regulation and
discipline of health professionals.
2. The executive director shall maintain a list of
appropriately qualified persons to whom an informal fact-finding proceeding may
be delegated.
3. The board may delegate to the executive director the
selection of the agency subordinate who is deemed appropriately qualified to
conduct a proceeding based on the qualifications of the subordinate and the
type of case being heard.
NOTICE: The following
forms used in administering the regulation were filed by the agency. The forms
are not being published; however, online users of this issue of the Virginia
Register of Regulations may click on the name of a form with a hyperlink to
access it. The forms are also available from the agency contact or may be
viewed at the Office of the Registrar of Regulations, General Assembly
Building, 2nd Floor, Richmond, Virginia 23219.
FORMS (18VAC30-21)
Continuing
Education Form (rev. 3/2015)
VA.R. Doc. No. R11-2759; Filed June 18, 2016, 11:21 a.m.
TITLE 18. PROFESSIONAL AND OCCUPATIONAL LICENSING
BOARD OF VETERINARY MEDICINE
Final Regulation
Title of Regulation: 18VAC150-20. Regulations
Governing the Practice of Veterinary Medicine (amending 18VAC150-20-70).
Statutory Authority: §§ 54.1-2400 and 54.1-3805.2
of the Code of Virginia.
Effective Date: August 10, 2016.
Agency Contact: Leslie L. Knachel, Executive Director,
Board of Veterinary Medicine, 9960 Mayland Drive, Suite 300, Richmond, VA
23233, telephone (804) 367-4468, FAX (804) 527-4471, or email
leslie.knachel@dhp.virginia.gov.
Summary:
The amendment increases the number of continuing education
hours required for renewal of a veterinary technician license to eight hours
per year.
Summary of Public Comments and Agency's Response: A
summary of comments made by the public and the agency's response may be
obtained from the promulgating agency or viewed at the office of the Registrar
of Regulations.
18VAC150-20-70. Licensure renewal requirements.
A. Every person licensed by the board shall, by January 1 of
every year, submit to the board a completed renewal application and pay to the
board a renewal fee as prescribed in 18VAC150-20-100. Failure to renew shall
cause the license to lapse and become invalid, and practice with a lapsed
license may subject the licensees to disciplinary action by the board. Failure
to receive a renewal notice does not relieve the licensee of his responsibility
to renew and maintain a current license.
B. Veterinarians shall be required to have completed a
minimum of 15 hours, and veterinary technicians shall be required to have
completed a minimum of six eight hours, of approved continuing
education for each annual renewal of licensure. Continuing education credits or
hours may not be transferred or credited to another year.
1. Approved continuing education credit shall be given for
courses or programs related to the treatment and care of patients and shall be
clinical courses in veterinary medicine or veterinary technology or courses
that enhance patient safety, such as medical recordkeeping or compliance with
requirements of the Occupational Health and Safety Administration (OSHA).
2. An approved continuing education course or program shall be
sponsored by one of the following:
a. The AVMA or its constituent and component/branch
associations, specialty organizations, and board certified specialists in good
standing within their specialty board;
b. Colleges of veterinary medicine approved by the AVMA
Council on Education;
c. International, national, or regional conferences of
veterinary medicine;
d. Academies or species specific interest groups of veterinary
medicine;
e. State associations of veterinary technicians;
f. North American Veterinary Technicians Association;
g. Community colleges with an approved program in veterinary
technology;
h. State or federal government agencies;
i. American Animal Hospital Association (AAHA) or its
constituent and component/branch associations;
j. Journals or veterinary information networks recognized by
the board as providing education in veterinary medicine or veterinary
technology; or
k. An organization or entity approved by the Registry of
Approved Continuing Education of the American Association of Veterinary State
Boards.
3. A licensee is exempt from completing continuing education
requirements and considered in compliance on the first renewal date following
his initial licensure by examination.
4. The board may grant an exemption for all or part of the
continuing education requirements due to circumstances beyond the control of
the licensee, such as temporary disability, mandatory military service, or
officially declared disasters.
5. The board may grant an extension for good cause of up to
one year for the completion of continuing education requirements upon written
request from the licensee prior to the renewal date. Such an extension shall
not relieve the licensee of the continuing education requirement.
6. Licensees are required to attest to compliance with
continuing education requirements on their annual license renewal and are
required to maintain original documents verifying the date and subject of the
program or course, the number of continuing education hours or credits, and
certification from an approved sponsor. Original documents must be maintained
for a period of two years following renewal. The board shall periodically conduct
a random audit to determine compliance. Practitioners selected for the audit
shall provide all supporting documentation within 10 days of receiving
notification of the audit.
7. Continuing education hours required by disciplinary order
shall not be used to satisfy renewal requirements.
C. A licensee who has requested that his license be placed on
inactive status is not authorized to perform acts that are considered the
practice of veterinary medicine or veterinary technology and, therefore, shall
not be required to have continuing education for annual renewal. To reactivate
a license, the licensee is required to submit evidence of completion of
continuing education hours as required by § 54.1-3805.2 of the Code of
Virginia equal to the number of years in which the license has not been active
for a maximum of two years.
VA.R. Doc. No. R14-18; Filed June 18, 2016, 11:18 a.m.
Therefore, by virtue of the authority vested in me as Governor,
and subject always to my continuing and ultimate authority and responsibility
to act in such matters, I hereby confirm, ratify, and memorialize in writing
that verbal directive issued on May 23, 2016, whereby it was determined that
the Department of Motor Vehicles suffered a disruption in service that
prevented the Department from processing applications for renewal of driver's
licenses.
In order to prevent any further hardship to the citizens of
Virginia, and in accordance with my authority contained in §§ 46.2-330 (A)
and 46.2-345 of the Code of Virginia, I hereby order the following measures:
I hereby direct the Commissioner of the Department of Motor
Vehicles, and such other executive branch agencies as deem appropriate in their
discretion, to extend the validity period of Virginia driver's license, permits
and commercial driver's licenses issued by the Commonwealth that expire May 21,
2016, through May 22, 2016, until May 28, 2016.
This Executive Order shall be effective retroactively from May
21, 2016, and shall remain in full force and effect until May 28, 2016.
Given under my hand and under the Seal of the Commonwealth of
Virginia, this 24th day of May, 2016.
Declaration of a State of Emergency
for the Commonwealth of Virginia Due to Severe Flooding
Therefore, by virtue of the authority vested in me by
§ 44-146.17 of the Code of Virginia, as Governor and as Director of
Emergency Management, and by virtue of the authority vested in me by Article V,
Section 7 of the Constitution of Virginia and by § 44-75.1 of the Code of
Virginia, as Governor and Commander-in-Chief of the armed forces of the
Commonwealth, and subject always to my continuing and ultimate authority and
responsibility to act in such matters, I hereby confirm, ratify, and
memorialize in writing my verbal orders issued on June 23, 2016, whereby I
proclaimed that a state of emergency exists, and I directed that appropriate
assistance be rendered by agencies of both state and local governments to
prepare for potential impacts of the flooding, alleviate any conditions
resulting from the incident, and to implement recovery and mitigation
operations and activities so as to return impacted areas to pre-event
conditions in so far as possible. Pursuant to § 44-75.1(A)(3) and (A)(4)
of the Code of Virginia, I also directed that the Virginia National Guard and
the Virginia Defense Force be called forth to state active duty to be prepared
to assist in providing such aid. This shall include Virginia National Guard
assistance to the Virginia Department of State Police to direct traffic,
prevent looting, and perform such other law enforcement functions as the
Superintendent of State Police, in consultation with the State Coordinator of
Emergency Management, the Adjutant General, and the Secretary of Public Safety
and Homeland Security, may find necessary.
In order to marshal all public resources and appropriate
preparedness, response, and recovery measures to meet this threat and recover
from its effects, and in accordance with my authority contained in
§ 44-146.17 of the Code of Virginia, I hereby order the following
protective and restoration measures:
B. Activation of the Virginia Emergency Operations Center
(VEOC) and the Virginia Emergency Support Team (VEST) to coordinate the
provision of assistance to local governments. I am directing that the VEOC and
VEST coordinate state actions in support of affected localities, other mission
assignments to agencies designated in the COVEOP, and others that may be
identified by the State Coordinator of Emergency Management, in consultation
with the Secretary of Public Safety and Homeland Security, which are needed to
provide for the preservation of life, protection of property, and
implementation of recovery activities.
C. The authorization to assume control over the Commonwealth's
state-operated telecommunications systems, as required by the State Coordinator
of Emergency Management, in coordination with the Virginia Information
Technologies Agency, and with the consultation of the Secretary of Public
Safety and Homeland Security, making all system assets available for use in
providing adequate communications, intelligence, and warning capabilities for
the incident, pursuant to § 44-146.18 of the Code of Virginia.
D. The evacuation of areas threatened or stricken by effects
of the flooding, as appropriate.
Following a declaration of a local emergency pursuant to
§ 44-146.21 of the Code of Virginia, if a local governing body determines
that evacuation is deemed necessary for the preservation of life or other
emergency mitigation, response, or recovery effort, pursuant to
§ 44-146.17(1) of the Code of Virginia, I direct the evacuation of all or
part of the populace therein from such areas and upon such timetable as the local
governing body, in coordination with the VEOC, acting on behalf of the State
Coordinator of Emergency Management, shall determine. Notwithstanding the
foregoing, I reserve the right to direct and compel evacuation from the same
and different areas and determine a different timetable both where local
governing bodies have made such a determination and where local governing
bodies have not made such a determination. Also, in those localities that have
declared a local emergency pursuant to § 44-146.21 of the Code of
Virginia, if the local governing body determines that controlling movement of
persons is deemed necessary for the preservation of life, public safety, or
other emergency mitigation, response, or recovery effort, pursuant to
§ 44-146.17(1) of the Code of Virginia, I authorize the control of ingress
and egress at an emergency area, including the movement of persons within the
area and the occupancy of premises therein upon such timetable as the local
governing body, in coordination with the State Coordinator of Emergency Management and
the VEOC, shall determine. Violations
of any order to citizens to evacuate shall constitute a violation of this
Executive Order and are punishable as a Class 1 misdemeanor.
E. The activation, implementation, and coordination of
appropriate mutual aid agreements and compacts, including the Emergency
Management Assistance Compact (EMAC), and the authorization of the State
Coordinator of Emergency Management to enter into any other supplemental
agreements, pursuant to § 44-146.17(5) and § 44-146.28:1 of the Code
of Virginia, to provide for the evacuation and reception of injured and other
persons and the exchange of medical, fire, police, National Guard personnel and
equipment, public utility, reconnaissance, welfare, transportation, and
communications personnel, equipment, and supplies. The State Coordinator of
Emergency Management is hereby designated as Virginia's authorized
representative within the meaning of the Emergency Management Assistance
Compact, § 44-146.28:1 of the Code of Virginia.
F. The authorization of the Departments of State Police,
Transportation, and Motor Vehicles to grant temporary overweight, over width,
registration, or license exemptions to all carriers transporting essential
emergency relief supplies, livestock or poultry, feed or other critical
supplies for livestock or poultry, heating oil, motor fuels, or propane, or
providing restoration of utilities (electricity, gas, phone, water, wastewater,
and cable) in and through any area of the Commonwealth in order to support the
disaster response and recovery, regardless of their point of origin or
destination. Such exemptions shall not be valid on posted structures for
restricted weight.
All over width loads, up to a maximum of 12 feet, and over
height loads up to a maximum of 14 feet must follow Virginia Department of
Motor Vehicles (DMV) hauling permit and safety guidelines.
In addition to described overweight/over width transportation
privileges, carriers are also exempt from registration with the Department of
Motor Vehicles. This includes vehicles en route and returning to their home
base. The above-cited agencies shall communicate this information to all staff
responsible for permit issuance and truck legalization enforcement.
Authorization of the State Coordinator of Emergency Management
to grant limited exemption of hours of service by any carrier when transporting
essential emergency relief supplies, passengers, property, livestock, poultry,
equipment, food, feed for livestock or poultry, fuel, construction materials,
and other critical supplies to or from any portion of the Commonwealth for
purpose of providing direct relief or assistance as a result of this disaster,
pursuant to § 52-8.4 of the Code of Virginia and Title 49 Code of Federal
Regulations, Section 390.23 and Section 395.3.
The foregoing overweight/over width transportation privileges
as well as the regulatory exemption provided by § 52-8.4(A) of the Code of
Virginia, and implemented in 19VAC30-20-40(B) of the
"Motor Carrier Safety Regulations,"
shall remain in effect for 30 days
from the onset of the disaster, or
until emergency relief is no longer necessary, as determined by the Secretary of Public Safety and
Homeland Security in Consultation with the Secretary of Transportation, whichever
is earlier.
G. The discontinuance of provisions authorized in paragraph F
above may be implemented and disseminated by publication of administrative
notice to all affected and interested parties. I hereby delegate to the
Secretary of Public Safety and Homeland Security, after consultation with other
affected Cabinet Secretaries, the authority to implement this order as set
forth in § 2.2-104 of the Code of Virginia.
H. The authorization of a maximum of $1,600,000 in state sum
sufficient funds for state and local government mission assignments authorized
and coordinated through the Virginia Department of Emergency Management that
are allowable as defined by The Stafford Act. This funding is also available
for state response and recovery operations and incident documentation. Out of
this state disaster sum sufficient, $100,000 or more if available, is
authorized for the Department of Military Affairs for the state's portion of
the eligible disaster related costs incurred for salaries, travel, and meals
during mission assignments authorized and coordinated through the Virginia
Department of Emergency Management.
I. The authorization of a maximum of $250,000 for matching
funds for the Individuals and Household Program, authorized by The Stafford Act
(when presidentially authorized), to be paid from state funds.
J. The implementation by public agencies under my supervision
and control of their emergency assignments as directed in the COVEOP without
regard to normal procedures pertaining to performance of public work, entering
into contracts, incurring of obligations or other logistical and support
measures of the Emergency Services and Disaster Laws, as provided in
§ 44-146.28(b) of the Code of Virginia. § 44-146.24 of the Code of
Virginia also applies to the disaster activities of state agencies.
K. Designation of members and personnel of volunteer,
auxiliary, and reserve groups including search and rescue (SAR), Virginia
Associations of Volunteer Rescue Squads (VAVRS), Civil Air Patrol (CAP), member
organizations of the Voluntary Organizations Active in Disaster (VOAD), Radio
Amateur Civil Emergency Services (RACES), volunteer fire fighters, Citizen
Corps Programs such as Medical Reserve Corps (MRCs), Community Emergency
Response Teams (CERT), and others identified and tasked by the State
Coordinator of Emergency Management for specific disaster related mission
assignments as representatives of the Commonwealth engaged in emergency
services activities within the meaning of the immunity provisions of
§ 44-146.23(a) and (f) of the Code of Virginia, in the performance of
their specific disaster-related mission assignments.
L. The authorization of appropriate oversight boards,
commissions, and agencies to
ease building code restrictions and to permit emergency demolition, hazardous waste disposal, debris removal, emergency
landfill sitting, and operations and
other activities necessary to address immediate health and safety needs without regard to time-consuming procedures or formalities and without
regard to application or
permit
fees or royalties.
M. The activation of the statutory provisions in
§ 59.1-525 et seq. of the Code of Virginia related to price gouging. Price
gouging at any time is unacceptable. Price gouging is even more reprehensible
during a time of disaster after issuance of a state of emergency. I have
directed all applicable executive branch agencies to take immediate action to
address any verified reports of price gouging of necessary goods or services. I
make the same request of the Office of the Attorney General and appropriate
local officials. I further request that all appropriate executive branch
agencies exercise their discretion to the extent allowed by law to address any
pending deadlines or expirations affected by or attributable to this disaster
event.
N. The following conditions apply to the deployment of the
Virginia National Guard and the Virginia Defense Force:
1. The Adjutant
General of Virginia, after consultation with the State Coordinator of
Emergency Management, shall make available on state active duty such units and members of
the Virginia National Guard and
Virginia Defense Force and such equipment as may be necessary or desirable
to assist in preparations for this
incident and in alleviating the human
suffering and damage to property.
2. Pursuant to § 52-6 of the Code of Virginia, I authorize the Superintendent of the Department
of State Police to appoint any and
all such Virginia Army and Air
National Guard personnel called to state active duty as additional police officers as deemed
necessary. These police officers
shall have the same powers and perform the
same duties as the State Police
officers appointed by the
Superintendent. However, they shall nevertheless remain members of
the Virginia National Guard, subject
to military command as members of the State Militia. Any bonds and/or insurance required by § 52-7 of the Code of Virginia shall be provided for them at the expense
of the Commonwealth.
3. In all instances,
members
of the Virginia National Guard and
Virginia Defense Force shall remain
subject to military command as prescribed by § 44-78.1 of the Code of Virginia and are not subject to the civilian authorities of county or municipal governments. This shall not be deemed
to prohibit working in close
cooperation with members of the Virginia Departments of State Police or Emergency
Management or local law enforcement or emergency
management authorities or receiving guidance from them in the performance of their duties.
4. Should service under this Executive Order result in the
injury or death of any member of the Virginia National Guard,
the following will be provided to the member
and the member's dependents or
survivors:
a. Workers' Compensation
benefits provided to members of the
National Guard by the Virginia Workers'
Compensation Act, subject to the requirements and limitations thereof; and, in
addition,
b. The same benefits, or their equivalent, for injury,
disability, and/or death, as would be provided by the federal government if the
member were serving on federal active duty at
the time of the injury or death. Any
such federal-type benefits due to a member and his or her dependents or survivors during any calendar month shall be reduced by any payments due under the Virginia Workers' Compensation Act during the same
month.
If and when the time period
for payment of Workers' Compensation benefits has elapsed, the member
and his or her dependents or
survivors shall thereafter receive full federal-type benefits for as long as they would have received
such benefits if the member had been serving on federal
active duty at the time of injury or
death. Any federal-type benefits due
shall be computed on the basis of military pay grade E-5 or the
member's military
grade at the time of injury or death, whichever produces the greater
benefit amount. Pursuant to § 44-14 of the Code of Virginia, and
subject to the availability of
future appropriations which may be lawfully
applied to this purpose, I now approve of future expenditures out of appropriations to the
Department of Military Affairs for such federal-type benefits as
being manifestly for the benefit of the military
service.
5. The following conditions apply to service by the Virginia Defense Force:
a. Compensation shall be at a daily rate that is equivalent of
base pay only for a National Guard Unit Training Assembly, commensurate with
the grade and years of service of the member, not to exceed 20 years of
service;
b. Lodging and meals shall be provided by the Adjutant General
or reimbursed at standard state per diem rates;
c. All privately owned equipment, including, but not limited
to, vehicles, boats, and aircraft, will be reimbursed for expense of fuel.
Damage or loss of said equipment will be reimbursed, minus reimbursement from
personal insurance, if said equipment was authorized for use by the Adjutant
General in accordance with § 44-54.12 of the Code of Virginia;
d. In the event of death or injury, benefits shall be provided
in accordance with the Virginia Workers' Compensation Act, subject to the
requirements and limitations thereof.
Given under my hand and under the Seal of the Commonwealth of
Virginia, this 24th day of June, 2016.