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. 18 - May 02, 2016
May 2016 through April 2017
Volume: Issue
|
Material Submitted By Noon*
|
Will Be Published On
|
32:18
|
April 13, 2016
|
May 2, 2016
|
32:19
|
April 27, 2016
|
May 16, 2016
|
32:20
|
May 11, 2016
|
May 30, 2016
|
32:21
|
May 25, 2016
|
June 13, 2016
|
32:22
|
June 8, 2016
|
June 27, 2016
|
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
|
*Filing deadlines are Wednesdays
unless otherwise specified.
PETITIONS FOR RULEMAKING
Vol. 32 Iss. 18 - May 02, 2016
TITLE 18. PROFESSIONAL AND
OCCUPATIONAL LICENSING
BOARD OF MEDICINE
Initial Agency Notice
Title of Regulation: 18VAC85-20.
Regulations Governing the Practice of Medicine, Osteopathic Medicine, Podiatry,
and Chiropractic.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: Mitch Gray.
Nature of Petitioner's Request: The petition for
rulemaking requests an amendment to requirements for standards for professional
conduct in the practice of medicine. Specifically, it requests the addition of
a requirement for physicians to wear gloves when conducting a genital
examination to protect both the patient against the perception of sexual
conduct and the physician against the transmission of sexually-transmitted
disease.
Agency Plan for Disposition of Request: In accordance
with Virginia law, the petition has been filed with the Registrar of
Regulations and will be published on May 2, 2016, and posted on the Virginia
Regulatory Town Hall at www.townhall.virginia.gov. Comment on the petition will
be requested until June 1, 2016, and may be posted on the Town Hall or sent to
the board. Following receipt of all comments on the petition to amend
regulations, the matter will be considered by the full board at its meeting on
June 16, 2016.
Public Comment Deadline: June 1, 2016.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-21; Filed April 5, 2016, 9:55 a.m.
BOARD OF NURSING
Initial Agency Notice
Title of Regulation: 18VAC90-20.
Regulations Governing the Practice of Nursing.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: Greg Huber.
Nature of Petitioner's Request: To eliminate the
allowance for a person to reactivate or reinstate a license by payment of the
required fee within one renewal cycle. The regulation appears to allow a person
to let his license lapse and then pay the reinstatement fee without meeting the
requirements for continued competency for renewal of licensure.
Agency Plan for Disposition of Request: In accordance
with Virginia law, the petition to amend the regulations has been filed with
the Registrar of Regulations for publication on May 2, 2016. It is also
posted on the Virginia Regulatory Town Hall at www.townhall.virginia.gov and
will be available for comment online on that date. Comment on the petition from
interested parties is requested until June 1, 2016. Following receipt of all
comments on the petition, the request to examine requirements for persons
reactivating or reinstating a license will be considered by the board at its
meeting on July 19, 2016.
Public Comment Deadline: June 1, 2016.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-22; Filed April 13, 2016, 10:34 a.m.
BOARD OF PHARMACY
Agency Decision
Title of Regulation: 18VAC110-20.
Regulations Governing the Practice of Pharmacy.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: Bill Irvin.
Nature of Petitioner's Request: To allow a pharmacy
providing services to a long-term care facility to provide prescription
information of Schedule VI drugs to a "back-up" pharmacy located near
the facility enabling the "back-up" pharmacy to provide the first
dispensing of the prescription without the act constituting a transfer of the
prescription.
Agency Decision: Request granted.
Statement of Reason for Decision: At its meeting on
March 25, 2016, the board considered the petition and the public comments in
support. Following a lengthy discussion, the board concluded it will include
the matter in the Notice of Intended Regulatory Action resulting from a
periodic review of regulations.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-10; Filed April 7, 2016, 2:03 p.m.
Agency Decision
Title of Regulation: 18VAC110-20.
Regulations Governing the Practice of Pharmacy.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: Angela Gilley.
Nature of Petitioner's Request: Within a hospital or
free-standing emergency department setting, the medical staff may approve
guidelines that are clinically accepted as the standard of care, or are
approved by the medical staff of the hospital through the typical approval
process (such as the pharmacy and therapeutics committee), which allow
pharmacists to change, discontinue, adjust, monitor, order pertinent labs, and
make subsequent adjustments to medications as applicable to the approved
guideline without requiring a physician order to implement the guideline. In
addition, a practitioner may write an order for "pharmacy to dose" a
medication, which allows the pharmacist to dose, monitor, order pertinent labs,
and make subsequent adjustments to any medication specified in the order based
on the pharmacist's clinical judgment.
Agency Decision: Request denied.
Statement of Reason for Decision: At its meeting on March
25, 2016, the board considered the petition; there were no public comments
received in support or in opposition. Following a lengthy discussion, the board
concluded that it needed additional information and research and some legal
advice from its board counsel. For that purpose, the petition was denied, but
the matter was referred to the Regulation Committee of the board for further
consideration. While the board does not intend to initiate rulemaking at this
time, the committee will further review the issue, which will include a
discussion of the statute relating to collaborative practice.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-11; Filed April 7, 2016, 2:01 p.m.
Agency Decision
Title of Regulation: 18VAC110-20.
Regulations Governing the Practice of Pharmacy.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: David Merryfield.
Nature of Petitioner's Request: To allow bar code and
RFID scanning to extend the pharmacist check, once the bar code or RFID scan
has been verified once for each product by a pharmacist.
Agency Decision: Request denied.
Statement of Reason for Decision: At its meeting on
March 25, 2016, the board considered the petition; there were no public
comments received in support or in opposition. Following a lengthy discussion,
the board denied the request in the petition since there is a mechanism through
the consideration of an innovative (pilot) program for use of this technology
in lieu of pharmacist verification. In order to accomplish the recommended
change, the petitioner could consider submitting an application for the pilot
process with specificity for the practice proposed. Additionally, the
petitioner was reminded that one may currently use bar code and RFID technology
to assist staff in the dispensing process; however it cannot replace the
required pharmacist verification of accuracy. While the board does not intend
to initiate rulemaking at this time, the board will continue to test out
efficiencies and innovation in pharmacy practice through pilots for which the
results can inform policy decisions.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-12; Filed April 7, 2016, 2:05 p.m.
BOARD OF SOCIAL WORK
Agency Decision
Title of Regulation:
18VAC140-20. Regulations Governing the Practice of Social Work.
Statutory Authority: § 54.1-2400 of the Code of
Virginia.
Name of Petitioner: Anjaulyeke Bryant-Covert.
Nature of Petitioner's Request: To amend section
18VAC140-20-70 to allow persons who have failed the licensing examination to
count their supervision hours beyond the two years currently prescribed. The
amendment would grandfather those applicants who do not meet current
requirements for registration of supervision.
Agency Decision: Request denied.
Statement of Reason for Decision: At its meeting on
March 25, 2016, the board considered the petition; there were two public
comments received in support. Following a lengthy discussion, the board
concluded that the petitioner's supervised experience was approved prior to
initially sitting for the licensure examination. While a person is required to
re-apply if he does not pass the licensure examination within two years,
18VAC140-20-70 specifies a timeframe within which supervised experience that
was not pre-registered and approved could be accepted. Therefore, the board
does not believe an amendment to regulation is necessary to accomplish the
request and has declined to initiate rulemaking.
Agency Contact: Elaine J. Yeatts, Agency Regulatory
Coordinator, Department of Health Professions, 9960 Mayland Drive, Richmond,
VA 23233, telephone (804) 367-4688, or email elaine.yeatts@dhp.virginia.gov.
VA.R. Doc. No. R16-08; Filed April 7, 2016, 1:59 p.m.
REGULATIONS
Vol. 32 Iss. 18 - May 02, 2016
TITLE 8. EDUCATION
STATE COUNCIL OF HIGHER EDUCATION FOR VIRGINIA
Fast-Track Regulation
Title of Regulation: 8VAC40-50. Virginia Work-Study
Program Regulations (repealing 8VAC40-50-10 through
8VAC40-50-250).
Statutory Authority: § 23-38.70 of the Code of
Virginia (Repealed).
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: June 1, 2016.
Effective Date: June 30, 2016.
Agency Contact: Lee Ann Rung, Manager, Executive and
Council Affairs, State Council of Higher Education for Virginia, James Monroe
Building, 101 North 14th Street, 9th Floor, Richmond, VA 23219, telephone (804)
225-2602, FAX (804) 371-7911, or email leeannrung@schev.edu.
Basis: Section 23-9.6:1 of the Code of Virginia
authorizes the State Council of Higher Education for Virginia to adopt
regulations it believes necessary to implement all of the council's duties and
responsibilities as set forth in the Code of Virginia. Section 23-38.70 of the
Code of Virginia, which provided for the regulations to implement the Virginia
Work-Study Program, was repealed by Chapter 51 of the 2006 Acts of Assembly.
Purpose: The Virginia Work-Study Program has not existed
for at least 10 years, and the statutory authority for the program has been
repealed by the General Assembly, therefore it is necessary to repeal the
regulations. Repealing the regulations should not impact public health, safety,
or welfare.
Rationale for Using the Fast-Track Rulemaking Process:
Repealing regulations for a program that is no longer funded or authorized by
the General Assembly is not expected to be controversial.
Substance: The Virginia Work-Study Program Regulations
(8VAC40-50) are being repealed.
Issues: Repealing the regulations should eliminate any
confusion about the existence of the program. There are no other known
advantages or disadvantages to the agency or the public.
Department of Planning and
Budget's Economic Impact Analysis:
Summary of the Proposed Amendments to Regulation. The State
Council of Higher Education for Virginia proposes to repeal this regulation.
Result of Analysis. The benefits likely exceed the costs for
all proposed changes.
Estimated Economic Impact. The statutory authority for the
Virginia Work-Study Program was revoked by Chapter 51, Acts of Assembly of
2006. The program is no longer functional and has not received appropriations
since prior to 2006. Repealing this regulation would have no impact beyond a
small benefit from reducing the chance that someone would be misled concerning
the existence of the program by seeing the regulation.
Businesses and Entities Affected. The program has not
existed for at least ten years. Repealing the regulation 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 State
Council of Higher Education for Virginia concurs.
Summary:
Chapter 51 of the 2006 Acts of Assembly repealed Chapter
4.7 (§ 23-38.70 et seq.) of Title 23 of the Code of Virginia, relating to
the Virginia Work-Study Program. Given the repeal of the statutory basis for
the regulations implementing the program, this action repeals the Virginia
Work-Study Program Regulations.
VA.R. Doc. No. R16-4480; Filed April 4, 2016, 9:17 a.m.
TITLE 9. ENVIRONMENT
STATE AIR POLLUTION CONTROL BOARD
Final Regulation
REGISTRAR'S NOTICE: The
following regulatory action is exempt from Article 2 of the Administrative
Process Act in accordance with § 2.2-4006 A 4 c of the Code of Virginia,
which excludes regulations that are necessary to meet the requirements of
federal law or regulations, provided such regulations do not differ materially
from those required by federal law or regulation. In addition, the State Air
Pollution Control Board is claiming an exemption from Article 2 of the
Administrative Process Act in accordance with § 2.2-4006 A 3 of the
Code of Virginia, which excludes regulations that consist only of changes in
style or form or corrections of technical errors The State Air Pollution Control
Board will receive, consider, and respond to petitions by any interested person
at any time with respect to reconsideration or revision.
Title of Regulation: 9VAC5-20. General Provisions (Rev.
B16) (amending 9VAC5-20-180).
Statutory Authority: § 10.1-1308 of the Code of
Virginia; §§ 110 and 182 of the federal Clean Air Act; 40 CFR Part 51.
Effective Date: June 1, 2016.
Agency Contact: Karen G. Sabasteanski, Department of
Environmental Quality, 629 East Main Street, P.O. Box 1105, Richmond, VA 23218,
telephone (804) 698-4426, FAX (804) 698-4510, or email
karen.sabasteanski@deq.virginia.gov.
Summary:
On June 12, 2015 (80 FR 33840), the U.S. Environmental
Protection Agency (EPA) issued a final State Implementation Plan (SIP) call
concerning treatment of excess emissions in state rules by sources
during periods of startup, shutdown, or malfunction (SSM), including Virginia's
SSM rules at 9VAC5-20-180 G. The U.S. Court of Appeals for the District of
Columbia Circuit in 2014 held that such provisions are illegal, and state plans
must be amended accordingly. Essentially, EPA finds that 9VAC5-20-180 G as
currently drafted creates an impermissible affirmative defense for violations
of emission limits, therefore the amendments to this section remove the
provisions allowing an affirmative defense.
9VAC5-20-180. Facility and control equipment maintenance or
malfunction.
A. The provisions of this section apply to periods of excess
emissions resulting from (i) the shutdown or bypassing, or both, of air
pollution control equipment for necessary scheduled maintenance and (ii)
malfunctions or other equipment failures of any affected facility or related
air pollution control equipment.
B. In case of shutdown or bypassing, or both, of air
pollution control equipment for necessary scheduled maintenance which results
in excess emissions for more than one hour, the intent to shut down such
equipment shall be reported to the board and local air pollution control
agency, if any, at least 24 hours prior to the planned shutdown. Such prior
notice shall include, but is not limited to, the following:
1. Identification of the specific facility to be taken out of
service as well as its location and permit or registration number;
2. The expected length of time that the air pollution control
equipment will be out of service;
3. The nature and quantity of emissions of air pollutants
likely to occur during the shutdown period; and
4. Measures that will be taken to minimize the length of the
shutdown and to negate the effect of the outage of the air pollution control
equipment.
C. In the event that any affected facility or related air
pollution control equipment fails or malfunctions in such a manner that may
cause excess emissions for more than one hour, the owner shall, as soon as
practicable but (i) no later than four daytime business hours after
the malfunction is discovered, notify the board by facsimile
transmission, telephone or telegraph of such failure or malfunction and shall
(ii) within two weeks 14 days provide a written statement
giving all pertinent facts, including the estimated duration of the breakdown and
the demonstrations in subsection G of this section. Owners subject to the
requirements of 9VAC5-40-50 C and 9VAC5-50-50 C are not required to provide the
written statement prescribed in this subsection for facilities subject to the
monitoring requirements of 9VAC5-40-40 and 9VAC5-50-40. When the condition
causing the failure or malfunction has been corrected and the facility or
control equipment is again in operation, the owner shall notify the board.
D. In the event that the breakdown period cited in subsection
C of this section exists or is expected to exist for 30 days or more, the owner
shall, as expeditiously as possible but no later than 30 days after the failure
or malfunction and semi-monthly thereafter until the failure or malfunction is
corrected, submit to the board a written report containing the following:
1. Identification of the specific facility that is affected as
well as its location and permit or registration number;
2. The expected length of time that the air pollution control
equipment will be out of service;
3. The nature and quantity of air pollutant emissions likely
to occur during the breakdown period;
4. Measures to be taken to reduce emissions to the lowest
amount practicable during the breakdown period;
5. A statement as to why the owner was unable to obtain repair
parts or perform repairs which would allow compliance with the Regulations for
the Control and Abatement of Air Pollution within 30 days of the malfunction or
failure;
6. An estimate, with reasons given, of the duration of the
shortage of repairs or repair parts which would allow compliance with the
Regulations for the Control and Abatement of Air Pollution; and
7. Any other pertinent information as may be requested by the
board.
E. The provisions of subsection D of this section shall not
apply beyond three months of the date of the malfunction or failure. Should the
breakdown period exist past the three-month period, the owner may apply for a
variance in accordance with 9VAC5-20-50 A.
F. The following special provisions govern facilities which
are subject to the provisions of Article 5 (9VAC5-50-400 et seq.) of Part II
of 9VAC5 Chapter 50, 9VAC5-50 or Article 1 (9VAC5-60-60 et seq.) of
9VAC5 Chapter 60, or Article 2 (9VAC5-60-90 et seq.) of 9VAC5 Chapter 60
Part II of 9VAC5-60:
1. For sources subject to the applicable subparts listed in
9VAC5-50-410, any provisions governing malfunctions shall be implemented
through this section. In cases where there are differences between the
provisions of this section and the provisions of 40 CFR Part 60, the more
restrictive provisions shall apply.
2. For sources subject to the applicable subparts listed in
9VAC5-60-70, any provisions governing malfunctions shall be implemented through
this section. In cases where there are differences between the provisions of
this section and the provisions of 40 CFR Part 61, the more restrictive
provisions shall apply.
3. For sources subject to the applicable subparts listed in
9VAC5-60-100, any provisions governing malfunctions shall be implemented
through this section. In cases where there are differences between the
provisions of this section and the provisions of 40 CFR Part 63, the more
restrictive provisions shall apply.
G. No violation of applicable emission standards or
monitoring requirements shall be judged to have taken place In
accordance with subsection C of this section, if the excess emissions or
cessation of monitoring activities is due to a malfunction, provided that
the owner may demonstrate the following:
1. The cause of the excess emissions or cessation of
monitoring activities meets the definition of malfunction provided in
9VAC5-10-20;
1. 2. The procedural requirements of this
section were met or the owner has submitted an acceptable application for a
variance, which is subsequently granted;
2. 3. The owner has taken expeditious and
reasonable measures to minimize emissions during the breakdown period;
3. 4. The owner has taken expeditious and
reasonable measures to correct the malfunction and return the facility to a
normal operation; and
4. 5. The source is in compliance with
related applicable emission standards or monitoring requirements at least
90% of the operating time over the most recent 12-month period.
H. Nothing in this section shall be construed as giving an
owner the right to increase temporarily the emission of pollutants or to
circumvent the emission standards or monitoring requirements otherwise provided
in the Regulations for the Control and Abatement of Air Pollution.
I. Regardless of any other provision of this section, the
owner of any facility subject to the Regulations for the Control and Abatement
of Air Pollution shall, upon request of the board, reduce the level of
operation at the facility if the board determines that this is necessary to
prevent a violation of any primary ambient air quality standard. Under worst
case conditions, the board may order that the owner shut down the facility,
if there is no other method of operation to avoid a violation of the primary
ambient air quality standard. The board reserves the right to prescribe the
method of determining if a facility will cause such a violation. In such cases,
the facility shall not be returned to operation until it and the associated air
pollution control equipment are able to operate without violation of any
primary ambient air quality standard.
J. Any owner of an affected facility subject to the
provisions of this section shall maintain records of the occurrence and
duration of any bypass, malfunction, shutdown or failure of the facility or its
associated air pollution control equipment that results in excess emissions for
more than one hour. The records shall be maintained in a form suitable for
inspection and maintained for at least two years (unless a longer period is
specified in the applicable emission standard) following the date of the occurrence.
VA.R. Doc. No. R16-4598; Filed March 31, 2016, 11:04 a.m.
TITLE 9. ENVIRONMENT
STATE AIR POLLUTION CONTROL BOARD
Final Regulation
REGISTRAR'S NOTICE: The
following regulatory action is exempt from Article 2 of the Administrative
Process Act in accordance with § 2.2-4006 A 4 c of the Code of Virginia,
which excludes regulations that are necessary to meet the requirements of
federal law or regulations, provided such regulations do not differ materially
from those required by federal law or regulation. The State Air Pollution
Control Board will receive, consider, and respond to petitions by any
interested person at any time with respect to reconsideration or revision.
Titles of Regulations: 9VAC5-20. General Provisions (Rev.
A16) (amending 9VAC5-20-21).
9VAC5-30. Ambient Air Quality Standards (Rev. A16) (adding 9VAC5-30-57).
Statutory Authority: § 10.1-1308 of the Code of
Virginia; §§ 108, 109, and 302 of the federal Clean Air Act; 40 CFR
Parts 50, 53, and 58.
Effective Date: June 1, 2016.
Agency Contact: Karen G. Sabasteanski, Department of
Environmental Quality, 629 East Main Street, P.O. Box 1105, Richmond, VA 23218,
telephone (804) 698-4426, FAX (804) 698-4510, TTY (804) 698-4021,
or email karen.sabasteanski@deq.virginia.gov.
Summary:
On October 26, 2015 (80 FR 65292), the U.S. Environmental
Protection Agency (EPA) revised the ozone national ambient air quality standard
(NAAQS) by adding an 8-hour standard at a level of 0.070 parts per million
(ppm). The existing 8-hour standard of 0.075 ppm was not revoked. The new
primary standard became effective on December 28, 2015. 9VAC5-30 contains the
ambient air quality standards for the specific criteria pollutant standards set
out in 40 CFR Part 50 and is being amended to implement this EPA requirement.
In addition, a new Appendix U has been added. Appendix U explains the data
handling conventions and computations necessary for determining whether the NAAQS
for ozone are met at an ambient air quality monitoring site; this appendix is
incorporated by reference in 9VAC5-20-21. These regulations are amended
accordingly to properly implement new source permitting review and various
ozone implementation and planning programs.
9VAC5-20-21. Documents incorporated by reference.
A. The Administrative Process Act and Virginia Register Act
provide that state regulations may incorporate documents by reference.
Throughout these regulations, documents of the types specified below have been
incorporated by reference.
1. United States Code.
2. Code of Virginia.
3. Code of Federal Regulations.
4. Federal Register.
5. Technical and scientific reference documents.
Additional information on key federal regulations and
nonstatutory documents incorporated by reference and their availability may be
found in subsection E of this section.
B. Any reference in these regulations to any provision of the
Code of Federal Regulations (CFR) shall be considered as the adoption by
reference of that provision. The specific version of the provision adopted by
reference shall be that contained in the CFR (2014) in effect July 1, 2014. In
making reference to the Code of Federal Regulations, 40 CFR Part 35 means
Part 35 of Title 40 of the Code of Federal Regulations; 40 CFR 35.20 means
§ 35.20 in Part 35 of Title 40 of the Code of Federal Regulations.
C. Failure to include in this section any document referenced
in the regulations shall not invalidate the applicability of the referenced
document.
D. Copies of materials incorporated by reference in this
section may be examined by the public at the central office of the Department
of Environmental Quality, Eighth Floor, 629 East Main Street, Richmond,
Virginia, between 8:30 a.m. and 4:30 p.m. of each business day.
E. Information on federal regulations and nonstatutory
documents incorporated by reference and their availability may be found below
in this subsection.
1. Code of Federal Regulations.
a. The provisions specified below from the Code of Federal Regulations
(CFR) are incorporated herein by reference.
(1) 40 CFR Part 50 -- National Primary and Secondary Ambient
Air Quality Standards.
(a) Appendix A-1 -- Reference Measurement Principle and
Calibration Procedure for the Measurement of Sulfur Dioxide in the Atmosphere
(Ultraviolet Fluorescence Method).
(b) Appendix A-2 -- Reference Method for the Determination of
Sulfur Dioxide in the Atmosphere (Pararosaniline Method).
(c) Appendix B -- Reference Method for the Determination of
Suspended Particulate Matter in the Atmosphere (High-Volume Method).
(d) Appendix C -- Measurement Principle and Calibration
Procedure for the Continuous Measurement of Carbon Monoxide in the Atmosphere
(Non-Dispersive Infrared Photometry).
(e) Appendix D -- Measurement Principle and Calibration
Procedure for the Measurement of Ozone in the Atmosphere.
(f) Appendix E -- Reserved.
(g) Appendix F -- Measurement Principle and Calibration
Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas Phase
Chemiluminescence).
(h) Appendix G -- Reference Method for the Determination of
Lead in Suspended Particulate Matter Collected from Ambient Air.
(i) Appendix H -- Interpretation of the National Ambient Air
Quality Standards for Ozone.
(j) Appendix I -- Interpretation of the 8-Hour Primary and
Secondary National Ambient Air Quality Standards for Ozone.
(k) Appendix J -- Reference Method for the Determination of
Particulate Matter as PM10 in the Atmosphere.
(l) Appendix K -- Interpretation of the National Ambient Air
Quality Standards for Particulate Matter.
(m) Appendix L -- Reference Method for the Determination of
Fine Particulate Matter as PM2.5 in the Atmosphere.
(n) Appendix M -- Reserved.
(o) Appendix N -- Interpretation of the National Ambient Air
Quality Standards for PM2.5.
(p) Appendix O -- Reference Method for the Determination of
Coarse Particulate Matter as PM in the Atmosphere.
(q) Appendix P -- Interpretation of the Primary and Secondary
National Ambient Air Quality Standards for Ozone.
(r) Appendix Q -- Reference Method for the Determination of
Lead in Suspended Particulate Matter as PM10 Collected from Ambient
Air.
(s) Appendix R -- Interpretation of the National Ambient Air
Quality Standards for Lead.
(t) Appendix S -- Interpretation of the Primary National Ambient
Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide).
(u) Appendix T -- Interpretation of the Primary National
Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide).
(v) Appendix U -- Interpretation of the Primary and Secondary
National Ambient Air Quality Standards for Ozone.
(2) 40 CFR Part 51 -- Requirements for Preparation, Adoption,
and Submittal of Implementation Plans.
(a) Appendix M -- Recommended Test Methods for State
Implementation Plans.
(b) Appendix S -- Emission Offset Interpretive Ruling.
(c) Appendix W -- Guideline on Air Quality Models (Revised).
(d) Appendix Y -- Guidelines for BART Determinations Under the
Regional Haze Rule.
(3) 40 CFR Part 55 -- Outer Continental Shelf Air Regulations.
(4) 40 CFR Part 58 -- Ambient Air Quality Surveillance.
Appendix A -- Quality Assurance Requirements for SLAMS, SPMs
and PSD Air Monitoring.
(5) 40 CFR Part 59 -- National Volatile Organic Compound
Emission Standards for Consumer and Commercial Products.
(a) Subpart C -- National Volatile Organic Compound Emission
Standards for Consumer Products.
(b) Subpart D -- National Volatile Organic Compound Emission
Standards for Architectural Coatings, Appendix A -- Determination of Volatile
Matter Content of Methacrylate Multicomponent Coatings Used as Traffic Marking
Coatings.
(6) 40 CFR Part 60 -- Standards of Performance for New
Stationary Sources.
The specific provisions of 40 CFR Part 60 incorporated by
reference are found in Article 5 (9VAC5-50-400 et seq.) of Part II of 9VAC5-50 (New
and Modified Stationary Sources).
(7) 40 CFR Part 61 -- National Emission Standards for
Hazardous Air Pollutants.
The specific provisions of 40 CFR Part 61 incorporated by
reference are found in Article 1 (9VAC5-60-60 et seq.) of Part II of 9VAC5-60 (Hazardous
Air Pollutant Sources).
(8) 40 CFR Part 63 -- National Emission Standards for
Hazardous Air Pollutants for Source Categories.
The specific provisions of 40 CFR Part 63 incorporated by
reference are found in Article 2 (9VAC5-60-90 et seq.) of Part II of 9VAC5-60
(Hazardous Air Pollutant Sources).
(9) 40 CFR Part 64 -- Compliance Assurance Monitoring.
(10) 40 CFR Part 72 -- Permits Regulation.
(11) 40 CFR Part 73 -- Sulfur Dioxide Allowance System.
(12) 40 CFR Part 74 -- Sulfur Dioxide Opt-Ins.
(13) 40 CFR Part 75 -- Continuous Emission Monitoring.
(14) 40 CFR Part 76 -- Acid Rain Nitrogen Oxides Emission
Reduction Program.
(15) 40 CFR Part 77 -- Excess Emissions.
(16) 40 CFR Part 78 -- Appeal Procedures for Acid Rain
Program.
(17) 40 CFR Part 152 Subpart I -- Classification of
Pesticides.
(18) 49 CFR Part 172 -- Hazardous Materials Table. Special
Provisions, Hazardous Materials Communications, Emergency Response Information,
and Training Requirements, Subpart E, Labeling.
(19) 29 CFR Part 1926 Subpart F -- Fire Protection and
Prevention.
b. Copies may be obtained from: Superintendent of
Documents, P.O. Box 371954, Pittsburgh, Pennsylvania PA
15250-7954; phone telephone (202) 783-3238.
2. U.S. Environmental Protection Agency.
a. The following documents from the U.S. Environmental
Protection Agency are incorporated herein by reference:
(1) Reich Test, Atmospheric Emissions from Sulfuric Acid
Manufacturing Processes, Public Health Service Publication No. PB82250721,
1980.
(2) Compilation of Air Pollutant Emission Factors (AP-42).
Volume I: Stationary and Area Sources, stock number 055-000-00500-1, 1995;
Supplement A, stock number 055-000-00551-6, 1996; Supplement B, stock number
055-000-00565, 1997; Supplement C, stock number 055-000-00587-7, 1997; Supplement
D, 1998; Supplement E, 1999.
(3) "Guidelines for Determining Capture Efficiency"
(GD-35), Emissions Monitoring and Analysis Division, Office of Air Quality
Planning and Standards, January 9, 1995.
b. Copies of the document identified in subdivision E 2 a (1)
of this section, and Volume I and Supplements A through C of the document
identified in subdivision E 2 a (2) of this section, may be obtained from:
U.S. Department of Commerce, National Technical Information Service, 5285 Port
Royal Road, Springfield, Virginia VA 22161; phone telephone
1-800-553-6847. Copies of Supplements D and E of the document
identified in subdivision E 2 a (2) of this section may be obtained online from
EPA's Technology Transfer Network at http://www.epa.gov/ttn/index.html. Copies
of the document identified in subdivision E 2 a (3) of this section are only
available online from EPA's Technology Transfer Network at http://www.epa.gov/ttn/emc/guidlnd.html.
3. U.S. United States government.
a. The following document from the U.S. United
States government is incorporated herein by reference: Standard Industrial
Classification Manual, 1987 (U.S. Government Printing Office stock number 041-001-00-314-2).
b. Copies may be obtained from: Superintendent of
Documents, P.O. Box 371954, Pittsburgh, Pennsylvania PA
15250-7954; phone telephone (202) 512-1800.
4. American Society for Testing
and Materials (ASTM).
a. The documents specified below from the American Society for
Testing and Materials are incorporated herein by reference.
(1) D323-99a, "Standard Test Method for Vapor
Pressure of Petroleum Products (Reid Method)."
(2) D97-96a, "Standard Test Method for Pour Point
of Petroleum Products."
(3) D129-00, "Standard Test Method for Sulfur in
Petroleum Products (General Bomb Method)."
(4) D388-99, "Standard Classification of Coals by
Rank."
(5) D396-98, "Standard Specification for Fuel
Oils."
(6) D975-98b, "Standard Specification for Diesel
Fuel Oils."
(7) D1072-90(1999), "Standard Test Method for Total
Sulfur in Fuel Gases."
(8) D1265-97, "Standard Practice for Sampling
Liquefied Petroleum (LP) Gases (Manual Method)."
(9) D2622-98, "Standard Test Method for Sulfur in
Petroleum Products by Wavelength Dispersive X-Ray Fluorescence
Spectrometry."
(10) D4057-95(2000), "Standard Practice for Manual
Sampling of Petroleum and Petroleum Products."
(11) D4294-98, "Standard Test Method for Sulfur in
Petroleum and Petroleum Products by Energy-Dispersive X-Ray Fluorescence
Spectroscopy."
(12) D523-89, "Standard Test Method for Specular
Gloss" (1999).
(13) D1613-02, "Standard Test Method for Acidity in
Volatile Solvents and Chemical Intermediates Used in Paint, Varnish, Lacquer
and Related Products" (2002).
(14) D1640-95, "Standard Test Methods for Drying,
Curing, or Film Formation of Organic Coatings at Room Temperature" (1999).
(15) E119-00a, "Standard Test Methods for Fire
Tests of Building Construction Materials" (2000).
(16) E84-01, "Standard Test Method for Surface
Burning Characteristics of Building Construction Materials" (2001).
(17) D4214-98, "Standard Test Methods for
Evaluating the Degree of Chalking of Exterior Paint Films" (1998).
(18) D86-04b, "Standard Test Method for
Distillation of Petroleum Products at Atmospheric Pressure" (2004).
(19) D4359-90, "Standard Test Method for
Determining Whether a Material is a Liquid or a Solid" (reapproved 2000).
(20) E260-96, "Standard Practice for Packed Column
Gas Chromatography" (reapproved 2001).
(21) D3912-95, "Standard Test Method for Chemical
Resistance of Coatings Used in Light-Water Nuclear Power Plants"
(reapproved 2001).
(22) D4082-02, "Standard Test Method for Effects of
Gamma Radiation on Coatings for Use in Light-Water Nuclear Power Plants."
(23) F852-99, "Standard Specification for Portable
Gasoline Containers for Consumer Use" (reapproved 2006).
(24) F976-02, "Standard Specification for Portable
Kerosine and Diesel Containers for Consumer Use."
(25) D4457-02, "Standard Test Method for
Determination of Dichloromethane and 1,1,1-Trichloroethane in Paints and
Coatings by Direct Injection into a Gas Chromatograph" (reapproved 2008).
(26) D3792-05, "Standard Test Method for Water
Content of Coatings by Direct Injection Into a Gas Chromatograph."
(27) D2879-97, "Standard Test Method for Vapor
Pressure-Temperature Relationship and Initial Decomposition Temperature of
Liquids by Isoteniscope" (reapproved 2007).
b. Copies may be obtained from: American Society for
Testing Materials, 100 Barr Harbor Drive, West Conshohocken, Pennsylvania
PA 19428-2959; phone telephone (610) 832-9585.
5. American Petroleum Institute (API).
a. The following document from the American Petroleum
Institute is incorporated herein by reference: Evaporative Loss from Floating
Roof Tanks, API MPMS Chapter 19, April 1, 1997.
b. Copies may be obtained from: American Petroleum
Institute, 1220 L Street, Northwest, Washington, D.C. DC 20005; phone
telephone (202) 682-8000.
6. American Conference of Governmental Industrial Hygienists
(ACGIH).
a. The following document from the ACGIH is incorporated
herein by reference: 1991-1992 Threshold Limit Values for Chemical
Substances and Physical Agents and Biological Exposure Indices (ACGIH
Handbook).
b. Copies may be obtained from: ACGIH, 1330 Kemper
Meadow Drive, Suite 600, Cincinnati, Ohio OH 45240; phone telephone
(513) 742-2020.
7. National Fire Prevention Association (NFPA).
a. The documents specified below from the National Fire
Prevention Association are incorporated herein by reference.
(1) NFPA 385, Standard for Tank Vehicles for Flammable and
Combustible Liquids, 2000 Edition.
(2) NFPA 30, Flammable and Combustible Liquids Code, 2000
Edition.
(3) NFPA 30A, Code for Motor Fuel Dispensing Facilities and
Repair Garages, 2000 Edition.
b. Copies may be obtained from the National Fire Prevention
Association, One Batterymarch Park, P.O. Box 9101, Quincy, Massachusetts
MA 02269-9101; phone telephone (617) 770-3000.
8. American Society of Mechanical Engineers (ASME).
a. The documents specified below from the American Society of
Mechanical Engineers are incorporated herein by reference.
(1) ASME Power Test Codes: Test Code for Steam Generating
Units, Power Test Code 4.1-1964 (R1991).
(2) ASME Interim Supplement 19.5 on Instruments and Apparatus:
Application, Part II of Fluid Meters, 6th edition (1971).
(3) Standard for the Qualification and Certification of
Resource Recovery Facility Operators, ASME QRO-1-1994.
b. Copies may be obtained from the American Society of
Mechanical Engineers, Three Park Avenue, New York, New York NY
10016; phone telephone (800) 843-2763.
9. American Hospital Association (AHA).
a. The following document from the American Hospital Association
is incorporated herein by reference: An Ounce of Prevention: Waste Reduction
Strategies for Health Care Facilities, AHA Catalog no. W5-057007, 1993.
b. Copies may be obtained from: American Hospital
Association, One North Franklin, Chicago, IL 60606; phone telephone
(800) 242-2626.
10. Bay Area Air Quality Management District (BAAQMD).
a. The following documents from the Bay Area Air Quality
Management District are incorporated herein by reference:
(1) Method 41, "Determination of Volatile Organic Compounds
in Solvent-Based Coatings and Related Materials Containing
Parachlorobenzotrifluoride" (December 20, 1995).
(2) Method 43, "Determination of Volatile Methylsiloxanes
in Solvent-Based Coatings, Inks, and Related Materials" (November 6,
1996).
b. Copies may be obtained from: Bay Area Air Quality
Management District, 939 Ellis Street, San Francisco, CA 94109, phone telephone
(415) 771-6000.
11. South Coast Air Quality
Management District (SCAQMD).
a. The following documents from the South Coast Air Quality
Management District are incorporated herein by reference:
(1) Method 303-91, "Determination of Exempt
Compounds," in Manual SSMLLABM, "Laboratory Methods of Analysis for
Enforcement Samples" (1996).
(2) Method 318-95, "Determination of Weight Percent
Elemental Metal in Coatings by X-Ray Diffraction," in Manual SSMLLABM,
"Laboratory Methods of Analysis for Enforcement Samples" (1996).
(3) Rule 1174 Ignition Method Compliance Certification
Protocol (February 28, 1991).
(4) Method 304-91, "Determination of Volatile
Organic Compounds (VOC) in Various Materials," in Manual SSMLLABM,
"Laboratory Methods of Analysis for Enforcement Samples" (1996).
(5) Method 316A-92, "Determination of Volatile
Organic Compounds (VOC) in Materials Used for Pipes and Fittings" in
Manual SSMLLABM, "Laboratory Methods of Analysis for Enforcement
Samples" (1996).
(6) "General Test Method for Determining Solvent Losses
from Spray Gun Cleaning Systems," October 3, 1989.
b. Copies may be obtained from: South Coast Air Quality
Management District, 21865 E. Copley Drive, Diamond Bar, CA 91765, phone
telephone (909) 396-2000.
12. California Air Resources Board (CARB).
a. The following documents from the California Air Resources
Board are incorporated herein by reference:
(1) Test Method 510, "Automatic Shut-Off Test Procedure
for Spill-Proof Systems and Spill-Proof Spouts" (July 6, 2000).
(2) Test Method 511, "Automatic Closure Test Procedure
for Spill-Proof Systems and Spill-Proof Spouts" (July 6, 2000).
(3) Method 100, "Procedures for Continuous Gaseous
Emission Stack Sampling" (July 28, 1997).
(4) Test Method 513, "Determination of Permeation Rate
for Spill-Proof Systems" (July 6, 2000).
(5) Method 310, "Determination of Volatile Organic
Compounds (VOC) in Consumer Products and Reactive Organic Compounds in Aerosol
Coating Products (Including Appendices A and B)" (May 5, 2005).
(6) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 1, § 94503.5 (2003).
(7) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 2, §§ 94509 and 94511 (2003).
(8) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 4, §§ 94540-94555 (2003).
(9) "Certification Procedure 501 for Portable Fuel
Containers and Spill-Proof Spouts, CP-501" (July 26, 2006).
(10) "Test Procedure for Determining Integrity of
Spill-Proof Spouts and Spill-Proof Systems, TP-501" (July 26, 2006).
(11) "Test Procedure for Determining Diurnal Emissions
from Portable Fuel Containers, TP-502" (July 26, 2006).
b. Copies may be obtained from: California Air
Resources Board, P.O. Box 2815, Sacramento, CA 95812, phone telephone
(906) 322-3260 or (906) 322-2990.
13. American Architectural Manufacturers Association.
a. The following documents from the American Architectural
Manufacturers Association are incorporated herein by reference:
(1) Voluntary Specification 2604-02, "Performance
Requirements and Test Procedures for High Performance Organic Coatings on
Aluminum Extrusions and Panels" (2002).
(2) Voluntary Specification 2605-02, "Performance
Requirements and Test Procedures for Superior Performing Organic Coatings on
Aluminum Extrusions and Panels" (2002).
b. Copies may be obtained from: American Architectural
Manufacturers Association, 1827 Walden Office Square, Suite 550, Schaumburg, IL
60173, phone telephone (847) 303-5664.
14. American Furniture Manufacturers Association.
a. The following document from the American Furniture
Manufacturers Association is incorporated herein by reference: Joint Industry
Fabrics Standards Committee, Woven and Knit Residential Upholstery Fabric
Standards and Guidelines (January 2001).
b. Copies may be obtained from: American Furniture
Manufacturers Association, P.O. Box HP-7, High Point, NC 27261; phone telephone
(336) 884-5000.
15. Petroleum Equipment Institute.
a. The following document from the Petroleum Equipment
Institute is incorporated herein by reference: Recommended Practices for
Installation and Testing of Vapor-Recovery Systems at Vehicle-Fueling Sites,
PEI/RP300-09 (2009).
b. Copies may be obtained from: Petroleum Equipment
Institute, 6931 S. 66th E. Avenue, Suite 310, Tulsa, OK 74133; telephone (918)
494-9696; www.pei.org.
16. American Architectural
Manufacturers Association (AAMA).
a. The following documents from the American Architectural
Manufacturers Association are incorporated herein by reference:
(1) Voluntary Specification, Performance Requirements and Test
Procedures for High Performance Organic Coatings on Aluminum Extrusions and
Panels, publication number AAMA 2604-05.
(2) Voluntary Specification, Performance Requirements and Test
Procedures for Superior Performing Organic Coatings on Aluminum Extrusions and
Panels, publication number AAMA 2605-05.
b. Copies may be obtained from: American Architectural
Manufacturers Association, 1827 Walden Office Square, Suite 550, Schaumburg, IL
60173-4268; phone 847- telephone (847) 303-5774.
9VAC5-30-57. Ozone (8-hour, 0.070 ppm).
A. The primary and secondary ambient air quality standard
is 0.070 parts per million, daily maximum 8-hour average.
B. Ozone shall be measured by a reference method based on
Appendix D to 40 CFR Part 50 and designated in accordance with 40 CFR Part 53
or an equivalent method designated in accordance with 40 CFR Part 53.
C. The primary and secondary ambient air quality standards
are met at an ambient air quality monitoring site when the 3-year average of
the annual fourth-highest daily maximum 8-hour average ozone concentration is
less than or equal to 0.070 ppm, as determined in accordance with Appendix U to
40 CFR Part 50.
VA.R. Doc. No. R16-4594; Filed March 31, 2016, 11:08 a.m.
TITLE 9. ENVIRONMENT
STATE AIR POLLUTION CONTROL BOARD
Final Regulation
REGISTRAR'S NOTICE: The
following regulatory action is exempt from Article 2 of the Administrative
Process Act in accordance with § 2.2-4006 A 4 c of the Code of Virginia,
which excludes regulations that are necessary to meet the requirements of
federal law or regulations, provided such regulations do not differ materially
from those required by federal law or regulation. The State Air Pollution
Control Board will receive, consider, and respond to petitions by any
interested person at any time with respect to reconsideration or revision.
Titles of Regulations: 9VAC5-20. General Provisions (Rev.
A16) (amending 9VAC5-20-21).
9VAC5-30. Ambient Air Quality Standards (Rev. A16) (adding 9VAC5-30-57).
Statutory Authority: § 10.1-1308 of the Code of
Virginia; §§ 108, 109, and 302 of the federal Clean Air Act; 40 CFR
Parts 50, 53, and 58.
Effective Date: June 1, 2016.
Agency Contact: Karen G. Sabasteanski, Department of
Environmental Quality, 629 East Main Street, P.O. Box 1105, Richmond, VA 23218,
telephone (804) 698-4426, FAX (804) 698-4510, TTY (804) 698-4021,
or email karen.sabasteanski@deq.virginia.gov.
Summary:
On October 26, 2015 (80 FR 65292), the U.S. Environmental
Protection Agency (EPA) revised the ozone national ambient air quality standard
(NAAQS) by adding an 8-hour standard at a level of 0.070 parts per million
(ppm). The existing 8-hour standard of 0.075 ppm was not revoked. The new
primary standard became effective on December 28, 2015. 9VAC5-30 contains the
ambient air quality standards for the specific criteria pollutant standards set
out in 40 CFR Part 50 and is being amended to implement this EPA requirement.
In addition, a new Appendix U has been added. Appendix U explains the data
handling conventions and computations necessary for determining whether the NAAQS
for ozone are met at an ambient air quality monitoring site; this appendix is
incorporated by reference in 9VAC5-20-21. These regulations are amended
accordingly to properly implement new source permitting review and various
ozone implementation and planning programs.
9VAC5-20-21. Documents incorporated by reference.
A. The Administrative Process Act and Virginia Register Act
provide that state regulations may incorporate documents by reference.
Throughout these regulations, documents of the types specified below have been
incorporated by reference.
1. United States Code.
2. Code of Virginia.
3. Code of Federal Regulations.
4. Federal Register.
5. Technical and scientific reference documents.
Additional information on key federal regulations and
nonstatutory documents incorporated by reference and their availability may be
found in subsection E of this section.
B. Any reference in these regulations to any provision of the
Code of Federal Regulations (CFR) shall be considered as the adoption by
reference of that provision. The specific version of the provision adopted by
reference shall be that contained in the CFR (2014) in effect July 1, 2014. In
making reference to the Code of Federal Regulations, 40 CFR Part 35 means
Part 35 of Title 40 of the Code of Federal Regulations; 40 CFR 35.20 means
§ 35.20 in Part 35 of Title 40 of the Code of Federal Regulations.
C. Failure to include in this section any document referenced
in the regulations shall not invalidate the applicability of the referenced
document.
D. Copies of materials incorporated by reference in this
section may be examined by the public at the central office of the Department
of Environmental Quality, Eighth Floor, 629 East Main Street, Richmond,
Virginia, between 8:30 a.m. and 4:30 p.m. of each business day.
E. Information on federal regulations and nonstatutory
documents incorporated by reference and their availability may be found below
in this subsection.
1. Code of Federal Regulations.
a. The provisions specified below from the Code of Federal Regulations
(CFR) are incorporated herein by reference.
(1) 40 CFR Part 50 -- National Primary and Secondary Ambient
Air Quality Standards.
(a) Appendix A-1 -- Reference Measurement Principle and
Calibration Procedure for the Measurement of Sulfur Dioxide in the Atmosphere
(Ultraviolet Fluorescence Method).
(b) Appendix A-2 -- Reference Method for the Determination of
Sulfur Dioxide in the Atmosphere (Pararosaniline Method).
(c) Appendix B -- Reference Method for the Determination of
Suspended Particulate Matter in the Atmosphere (High-Volume Method).
(d) Appendix C -- Measurement Principle and Calibration
Procedure for the Continuous Measurement of Carbon Monoxide in the Atmosphere
(Non-Dispersive Infrared Photometry).
(e) Appendix D -- Measurement Principle and Calibration
Procedure for the Measurement of Ozone in the Atmosphere.
(f) Appendix E -- Reserved.
(g) Appendix F -- Measurement Principle and Calibration
Procedure for the Measurement of Nitrogen Dioxide in the Atmosphere (Gas Phase
Chemiluminescence).
(h) Appendix G -- Reference Method for the Determination of
Lead in Suspended Particulate Matter Collected from Ambient Air.
(i) Appendix H -- Interpretation of the National Ambient Air
Quality Standards for Ozone.
(j) Appendix I -- Interpretation of the 8-Hour Primary and
Secondary National Ambient Air Quality Standards for Ozone.
(k) Appendix J -- Reference Method for the Determination of
Particulate Matter as PM10 in the Atmosphere.
(l) Appendix K -- Interpretation of the National Ambient Air
Quality Standards for Particulate Matter.
(m) Appendix L -- Reference Method for the Determination of
Fine Particulate Matter as PM2.5 in the Atmosphere.
(n) Appendix M -- Reserved.
(o) Appendix N -- Interpretation of the National Ambient Air
Quality Standards for PM2.5.
(p) Appendix O -- Reference Method for the Determination of
Coarse Particulate Matter as PM in the Atmosphere.
(q) Appendix P -- Interpretation of the Primary and Secondary
National Ambient Air Quality Standards for Ozone.
(r) Appendix Q -- Reference Method for the Determination of
Lead in Suspended Particulate Matter as PM10 Collected from Ambient
Air.
(s) Appendix R -- Interpretation of the National Ambient Air
Quality Standards for Lead.
(t) Appendix S -- Interpretation of the Primary National Ambient
Air Quality Standards for Oxides of Nitrogen (Nitrogen Dioxide).
(u) Appendix T -- Interpretation of the Primary National
Ambient Air Quality Standards for Oxides of Sulfur (Sulfur Dioxide).
(v) Appendix U -- Interpretation of the Primary and Secondary
National Ambient Air Quality Standards for Ozone.
(2) 40 CFR Part 51 -- Requirements for Preparation, Adoption,
and Submittal of Implementation Plans.
(a) Appendix M -- Recommended Test Methods for State
Implementation Plans.
(b) Appendix S -- Emission Offset Interpretive Ruling.
(c) Appendix W -- Guideline on Air Quality Models (Revised).
(d) Appendix Y -- Guidelines for BART Determinations Under the
Regional Haze Rule.
(3) 40 CFR Part 55 -- Outer Continental Shelf Air Regulations.
(4) 40 CFR Part 58 -- Ambient Air Quality Surveillance.
Appendix A -- Quality Assurance Requirements for SLAMS, SPMs
and PSD Air Monitoring.
(5) 40 CFR Part 59 -- National Volatile Organic Compound
Emission Standards for Consumer and Commercial Products.
(a) Subpart C -- National Volatile Organic Compound Emission
Standards for Consumer Products.
(b) Subpart D -- National Volatile Organic Compound Emission
Standards for Architectural Coatings, Appendix A -- Determination of Volatile
Matter Content of Methacrylate Multicomponent Coatings Used as Traffic Marking
Coatings.
(6) 40 CFR Part 60 -- Standards of Performance for New
Stationary Sources.
The specific provisions of 40 CFR Part 60 incorporated by
reference are found in Article 5 (9VAC5-50-400 et seq.) of Part II of 9VAC5-50 (New
and Modified Stationary Sources).
(7) 40 CFR Part 61 -- National Emission Standards for
Hazardous Air Pollutants.
The specific provisions of 40 CFR Part 61 incorporated by
reference are found in Article 1 (9VAC5-60-60 et seq.) of Part II of 9VAC5-60 (Hazardous
Air Pollutant Sources).
(8) 40 CFR Part 63 -- National Emission Standards for
Hazardous Air Pollutants for Source Categories.
The specific provisions of 40 CFR Part 63 incorporated by
reference are found in Article 2 (9VAC5-60-90 et seq.) of Part II of 9VAC5-60
(Hazardous Air Pollutant Sources).
(9) 40 CFR Part 64 -- Compliance Assurance Monitoring.
(10) 40 CFR Part 72 -- Permits Regulation.
(11) 40 CFR Part 73 -- Sulfur Dioxide Allowance System.
(12) 40 CFR Part 74 -- Sulfur Dioxide Opt-Ins.
(13) 40 CFR Part 75 -- Continuous Emission Monitoring.
(14) 40 CFR Part 76 -- Acid Rain Nitrogen Oxides Emission
Reduction Program.
(15) 40 CFR Part 77 -- Excess Emissions.
(16) 40 CFR Part 78 -- Appeal Procedures for Acid Rain
Program.
(17) 40 CFR Part 152 Subpart I -- Classification of
Pesticides.
(18) 49 CFR Part 172 -- Hazardous Materials Table. Special
Provisions, Hazardous Materials Communications, Emergency Response Information,
and Training Requirements, Subpart E, Labeling.
(19) 29 CFR Part 1926 Subpart F -- Fire Protection and
Prevention.
b. Copies may be obtained from: Superintendent of
Documents, P.O. Box 371954, Pittsburgh, Pennsylvania PA
15250-7954; phone telephone (202) 783-3238.
2. U.S. Environmental Protection Agency.
a. The following documents from the U.S. Environmental
Protection Agency are incorporated herein by reference:
(1) Reich Test, Atmospheric Emissions from Sulfuric Acid
Manufacturing Processes, Public Health Service Publication No. PB82250721,
1980.
(2) Compilation of Air Pollutant Emission Factors (AP-42).
Volume I: Stationary and Area Sources, stock number 055-000-00500-1, 1995;
Supplement A, stock number 055-000-00551-6, 1996; Supplement B, stock number
055-000-00565, 1997; Supplement C, stock number 055-000-00587-7, 1997; Supplement
D, 1998; Supplement E, 1999.
(3) "Guidelines for Determining Capture Efficiency"
(GD-35), Emissions Monitoring and Analysis Division, Office of Air Quality
Planning and Standards, January 9, 1995.
b. Copies of the document identified in subdivision E 2 a (1)
of this section, and Volume I and Supplements A through C of the document
identified in subdivision E 2 a (2) of this section, may be obtained from:
U.S. Department of Commerce, National Technical Information Service, 5285 Port
Royal Road, Springfield, Virginia VA 22161; phone telephone
1-800-553-6847. Copies of Supplements D and E of the document
identified in subdivision E 2 a (2) of this section may be obtained online from
EPA's Technology Transfer Network at http://www.epa.gov/ttn/index.html. Copies
of the document identified in subdivision E 2 a (3) of this section are only
available online from EPA's Technology Transfer Network at http://www.epa.gov/ttn/emc/guidlnd.html.
3. U.S. United States government.
a. The following document from the U.S. United
States government is incorporated herein by reference: Standard Industrial
Classification Manual, 1987 (U.S. Government Printing Office stock number 041-001-00-314-2).
b. Copies may be obtained from: Superintendent of
Documents, P.O. Box 371954, Pittsburgh, Pennsylvania PA
15250-7954; phone telephone (202) 512-1800.
4. American Society for Testing
and Materials (ASTM).
a. The documents specified below from the American Society for
Testing and Materials are incorporated herein by reference.
(1) D323-99a, "Standard Test Method for Vapor
Pressure of Petroleum Products (Reid Method)."
(2) D97-96a, "Standard Test Method for Pour Point
of Petroleum Products."
(3) D129-00, "Standard Test Method for Sulfur in
Petroleum Products (General Bomb Method)."
(4) D388-99, "Standard Classification of Coals by
Rank."
(5) D396-98, "Standard Specification for Fuel
Oils."
(6) D975-98b, "Standard Specification for Diesel
Fuel Oils."
(7) D1072-90(1999), "Standard Test Method for Total
Sulfur in Fuel Gases."
(8) D1265-97, "Standard Practice for Sampling
Liquefied Petroleum (LP) Gases (Manual Method)."
(9) D2622-98, "Standard Test Method for Sulfur in
Petroleum Products by Wavelength Dispersive X-Ray Fluorescence
Spectrometry."
(10) D4057-95(2000), "Standard Practice for Manual
Sampling of Petroleum and Petroleum Products."
(11) D4294-98, "Standard Test Method for Sulfur in
Petroleum and Petroleum Products by Energy-Dispersive X-Ray Fluorescence
Spectroscopy."
(12) D523-89, "Standard Test Method for Specular
Gloss" (1999).
(13) D1613-02, "Standard Test Method for Acidity in
Volatile Solvents and Chemical Intermediates Used in Paint, Varnish, Lacquer
and Related Products" (2002).
(14) D1640-95, "Standard Test Methods for Drying,
Curing, or Film Formation of Organic Coatings at Room Temperature" (1999).
(15) E119-00a, "Standard Test Methods for Fire
Tests of Building Construction Materials" (2000).
(16) E84-01, "Standard Test Method for Surface
Burning Characteristics of Building Construction Materials" (2001).
(17) D4214-98, "Standard Test Methods for
Evaluating the Degree of Chalking of Exterior Paint Films" (1998).
(18) D86-04b, "Standard Test Method for
Distillation of Petroleum Products at Atmospheric Pressure" (2004).
(19) D4359-90, "Standard Test Method for
Determining Whether a Material is a Liquid or a Solid" (reapproved 2000).
(20) E260-96, "Standard Practice for Packed Column
Gas Chromatography" (reapproved 2001).
(21) D3912-95, "Standard Test Method for Chemical
Resistance of Coatings Used in Light-Water Nuclear Power Plants"
(reapproved 2001).
(22) D4082-02, "Standard Test Method for Effects of
Gamma Radiation on Coatings for Use in Light-Water Nuclear Power Plants."
(23) F852-99, "Standard Specification for Portable
Gasoline Containers for Consumer Use" (reapproved 2006).
(24) F976-02, "Standard Specification for Portable
Kerosine and Diesel Containers for Consumer Use."
(25) D4457-02, "Standard Test Method for
Determination of Dichloromethane and 1,1,1-Trichloroethane in Paints and
Coatings by Direct Injection into a Gas Chromatograph" (reapproved 2008).
(26) D3792-05, "Standard Test Method for Water
Content of Coatings by Direct Injection Into a Gas Chromatograph."
(27) D2879-97, "Standard Test Method for Vapor
Pressure-Temperature Relationship and Initial Decomposition Temperature of
Liquids by Isoteniscope" (reapproved 2007).
b. Copies may be obtained from: American Society for
Testing Materials, 100 Barr Harbor Drive, West Conshohocken, Pennsylvania
PA 19428-2959; phone telephone (610) 832-9585.
5. American Petroleum Institute (API).
a. The following document from the American Petroleum
Institute is incorporated herein by reference: Evaporative Loss from Floating
Roof Tanks, API MPMS Chapter 19, April 1, 1997.
b. Copies may be obtained from: American Petroleum
Institute, 1220 L Street, Northwest, Washington, D.C. DC 20005; phone
telephone (202) 682-8000.
6. American Conference of Governmental Industrial Hygienists
(ACGIH).
a. The following document from the ACGIH is incorporated
herein by reference: 1991-1992 Threshold Limit Values for Chemical
Substances and Physical Agents and Biological Exposure Indices (ACGIH
Handbook).
b. Copies may be obtained from: ACGIH, 1330 Kemper
Meadow Drive, Suite 600, Cincinnati, Ohio OH 45240; phone telephone
(513) 742-2020.
7. National Fire Prevention Association (NFPA).
a. The documents specified below from the National Fire
Prevention Association are incorporated herein by reference.
(1) NFPA 385, Standard for Tank Vehicles for Flammable and
Combustible Liquids, 2000 Edition.
(2) NFPA 30, Flammable and Combustible Liquids Code, 2000
Edition.
(3) NFPA 30A, Code for Motor Fuel Dispensing Facilities and
Repair Garages, 2000 Edition.
b. Copies may be obtained from the National Fire Prevention
Association, One Batterymarch Park, P.O. Box 9101, Quincy, Massachusetts
MA 02269-9101; phone telephone (617) 770-3000.
8. American Society of Mechanical Engineers (ASME).
a. The documents specified below from the American Society of
Mechanical Engineers are incorporated herein by reference.
(1) ASME Power Test Codes: Test Code for Steam Generating
Units, Power Test Code 4.1-1964 (R1991).
(2) ASME Interim Supplement 19.5 on Instruments and Apparatus:
Application, Part II of Fluid Meters, 6th edition (1971).
(3) Standard for the Qualification and Certification of
Resource Recovery Facility Operators, ASME QRO-1-1994.
b. Copies may be obtained from the American Society of
Mechanical Engineers, Three Park Avenue, New York, New York NY
10016; phone telephone (800) 843-2763.
9. American Hospital Association (AHA).
a. The following document from the American Hospital Association
is incorporated herein by reference: An Ounce of Prevention: Waste Reduction
Strategies for Health Care Facilities, AHA Catalog no. W5-057007, 1993.
b. Copies may be obtained from: American Hospital
Association, One North Franklin, Chicago, IL 60606; phone telephone
(800) 242-2626.
10. Bay Area Air Quality Management District (BAAQMD).
a. The following documents from the Bay Area Air Quality
Management District are incorporated herein by reference:
(1) Method 41, "Determination of Volatile Organic Compounds
in Solvent-Based Coatings and Related Materials Containing
Parachlorobenzotrifluoride" (December 20, 1995).
(2) Method 43, "Determination of Volatile Methylsiloxanes
in Solvent-Based Coatings, Inks, and Related Materials" (November 6,
1996).
b. Copies may be obtained from: Bay Area Air Quality
Management District, 939 Ellis Street, San Francisco, CA 94109, phone telephone
(415) 771-6000.
11. South Coast Air Quality
Management District (SCAQMD).
a. The following documents from the South Coast Air Quality
Management District are incorporated herein by reference:
(1) Method 303-91, "Determination of Exempt
Compounds," in Manual SSMLLABM, "Laboratory Methods of Analysis for
Enforcement Samples" (1996).
(2) Method 318-95, "Determination of Weight Percent
Elemental Metal in Coatings by X-Ray Diffraction," in Manual SSMLLABM,
"Laboratory Methods of Analysis for Enforcement Samples" (1996).
(3) Rule 1174 Ignition Method Compliance Certification
Protocol (February 28, 1991).
(4) Method 304-91, "Determination of Volatile
Organic Compounds (VOC) in Various Materials," in Manual SSMLLABM,
"Laboratory Methods of Analysis for Enforcement Samples" (1996).
(5) Method 316A-92, "Determination of Volatile
Organic Compounds (VOC) in Materials Used for Pipes and Fittings" in
Manual SSMLLABM, "Laboratory Methods of Analysis for Enforcement
Samples" (1996).
(6) "General Test Method for Determining Solvent Losses
from Spray Gun Cleaning Systems," October 3, 1989.
b. Copies may be obtained from: South Coast Air Quality
Management District, 21865 E. Copley Drive, Diamond Bar, CA 91765, phone
telephone (909) 396-2000.
12. California Air Resources Board (CARB).
a. The following documents from the California Air Resources
Board are incorporated herein by reference:
(1) Test Method 510, "Automatic Shut-Off Test Procedure
for Spill-Proof Systems and Spill-Proof Spouts" (July 6, 2000).
(2) Test Method 511, "Automatic Closure Test Procedure
for Spill-Proof Systems and Spill-Proof Spouts" (July 6, 2000).
(3) Method 100, "Procedures for Continuous Gaseous
Emission Stack Sampling" (July 28, 1997).
(4) Test Method 513, "Determination of Permeation Rate
for Spill-Proof Systems" (July 6, 2000).
(5) Method 310, "Determination of Volatile Organic
Compounds (VOC) in Consumer Products and Reactive Organic Compounds in Aerosol
Coating Products (Including Appendices A and B)" (May 5, 2005).
(6) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 1, § 94503.5 (2003).
(7) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 2, §§ 94509 and 94511 (2003).
(8) California Code of Regulations, Title 17, Division 3,
Chapter 1, Subchapter 8.5, Article 4, §§ 94540-94555 (2003).
(9) "Certification Procedure 501 for Portable Fuel
Containers and Spill-Proof Spouts, CP-501" (July 26, 2006).
(10) "Test Procedure for Determining Integrity of
Spill-Proof Spouts and Spill-Proof Systems, TP-501" (July 26, 2006).
(11) "Test Procedure for Determining Diurnal Emissions
from Portable Fuel Containers, TP-502" (July 26, 2006).
b. Copies may be obtained from: California Air
Resources Board, P.O. Box 2815, Sacramento, CA 95812, phone telephone
(906) 322-3260 or (906) 322-2990.
13. American Architectural Manufacturers Association.
a. The following documents from the American Architectural
Manufacturers Association are incorporated herein by reference:
(1) Voluntary Specification 2604-02, "Performance
Requirements and Test Procedures for High Performance Organic Coatings on
Aluminum Extrusions and Panels" (2002).
(2) Voluntary Specification 2605-02, "Performance
Requirements and Test Procedures for Superior Performing Organic Coatings on
Aluminum Extrusions and Panels" (2002).
b. Copies may be obtained from: American Architectural
Manufacturers Association, 1827 Walden Office Square, Suite 550, Schaumburg, IL
60173, phone telephone (847) 303-5664.
14. American Furniture Manufacturers Association.
a. The following document from the American Furniture
Manufacturers Association is incorporated herein by reference: Joint Industry
Fabrics Standards Committee, Woven and Knit Residential Upholstery Fabric
Standards and Guidelines (January 2001).
b. Copies may be obtained from: American Furniture
Manufacturers Association, P.O. Box HP-7, High Point, NC 27261; phone telephone
(336) 884-5000.
15. Petroleum Equipment Institute.
a. The following document from the Petroleum Equipment
Institute is incorporated herein by reference: Recommended Practices for
Installation and Testing of Vapor-Recovery Systems at Vehicle-Fueling Sites,
PEI/RP300-09 (2009).
b. Copies may be obtained from: Petroleum Equipment
Institute, 6931 S. 66th E. Avenue, Suite 310, Tulsa, OK 74133; telephone (918)
494-9696; www.pei.org.
16. American Architectural
Manufacturers Association (AAMA).
a. The following documents from the American Architectural
Manufacturers Association are incorporated herein by reference:
(1) Voluntary Specification, Performance Requirements and Test
Procedures for High Performance Organic Coatings on Aluminum Extrusions and
Panels, publication number AAMA 2604-05.
(2) Voluntary Specification, Performance Requirements and Test
Procedures for Superior Performing Organic Coatings on Aluminum Extrusions and
Panels, publication number AAMA 2605-05.
b. Copies may be obtained from: American Architectural
Manufacturers Association, 1827 Walden Office Square, Suite 550, Schaumburg, IL
60173-4268; phone 847- telephone (847) 303-5774.
9VAC5-30-57. Ozone (8-hour, 0.070 ppm).
A. The primary and secondary ambient air quality standard
is 0.070 parts per million, daily maximum 8-hour average.
B. Ozone shall be measured by a reference method based on
Appendix D to 40 CFR Part 50 and designated in accordance with 40 CFR Part 53
or an equivalent method designated in accordance with 40 CFR Part 53.
C. The primary and secondary ambient air quality standards
are met at an ambient air quality monitoring site when the 3-year average of
the annual fourth-highest daily maximum 8-hour average ozone concentration is
less than or equal to 0.070 ppm, as determined in accordance with Appendix U to
40 CFR Part 50.
VA.R. Doc. No. R16-4594; Filed March 31, 2016, 11:08 a.m.
TITLE 12. HEALTH
STATE BOARD OF HEALTH
Proposed Regulation
Title of Regulation: 12VAC5-412. Regulations for
Licensure of Abortion Facilities (amending 12VAC5-412-10, 12VAC5-412-130,
12VAC5-412-230, 12VAC5-412-240, 12VAC5-412-250, 12VAC5-412-290, 12VAC5-412-370;
repealing 12VAC5-412-30).
Statutory Authority: §§ 32.1-12, 32.1-127, and
32.1-127.001 of the Code of Virginia.
Public Hearing Information:
June 13, 2016 - 10 a.m. - Perimeter Center, Board Room 2,
2nd Floor, 9960 Mayland Drive, Henrico, VA 23233
Public Comment Deadline: July 1, 2016.
Agency Contact: Erik Bodin, Director, Office of
Licensure and Certification, Department of Health, 9960 Mayland Drive, Suite
401, Richmond, VA 23233, telephone (804) 367-2109, FAX (804) 527-4502, or email
erik.bodin@vdh.virginia.gov.
Basis: The regulation is promulgated under the authority
of § 32.1-127 of the Code of Virginia. Section 32.1-127 of the Code of
Virginia requires the board to promulgate regulations including minimum
standards for (i) the construction and maintenance of hospitals, nursing homes,
and certified nursing facilities to ensure the environmental protection and the
life safety of its patients, employees, and the public; (ii) the operation,
staffing, and equipping of hospitals, nursing homes, and certified nursing
facilities; (iii) qualifications and training of staff of hospitals, nursing
homes, and certified nursing facilities, except those professionals licensed or
certified by the Department of Health Professions; (iv) conditions under which
a hospital or nursing home may provide medical and nursing services to patients
in their places of residence; and (v) policies related to infection prevention,
disaster preparedness, and facility security of hospitals, nursing homes, and
certified nursing facilities. Facilities in which five or more first trimester
abortions are performed per month are classified as a category of hospital for
the purposes of this requirement. (§ 32.1-127 B 1).
Section 32.1-127.001 requires the State Board of Health to
adopt minimum standards for design and construction that are consistent with
the current edition of the Guidelines for Design and Construction of Hospital
and Health Care Facilities, now the Guidelines for Design and Construction of
Hospitals and Outpatient Facilities.
Purpose: On May 12, 2014, Governor McAuliffe issued
Executive Directive 1 (2014), which directed the State Board of Health to
conduct a periodic review of 12VAC5-412, Regulations for Licensure of Abortion
Facilities. As a result of the review, the Department of Health determined it
was necessary to use the regulatory process to amend the regulations. This
regulatory action will amend the regulations to clarify the requirements for
parental consent, insert additional best practices regarding medical testing
and laboratory services, insert additional best practices regarding anesthesia
service, align the requirements regarding emergency services more specifically
with medical best practices, update the requirements for facility design and
construction, and make minor technical amendments.
The regulations are mandated by § 32.1-127 of the Code of
Virginia. The regulations ensure health and safety standards are maintained
throughout licensed facilities within the Commonwealth. The review of the
regulations was mandated by Executive Directive. Upon review, the Department of
Health found areas of the regulations which could be improved, therefore
protecting the health and safety of patients of these facilities to a higher
degree.
Substance: No new regulatory sections are being
proposed. The following amendments will be proposed:
Definitions - Technical change. Addition of the terms
"medication induced abortion" and "surgical abortion" in
order to tailor the facility design and construction guidelines more precisely
to the requirements of each facility.
Classification - Repeal the section. Unnecessary due to Code of
Virginia requirements.
Violation of this chapter or applicable law; denial,
revocation, or suspension of license - Amend this section to include guidance
issued by the Virginia Department of Health Office of Licensure and
Certification.
Patient services; patient counseling - Remove an unnecessary
restriction not required by the Code of Virginia. Clarify the requirements of
parental consent. Ensure all requirements of parental consent are within the
regulations. Make additional technical changes that are in line with medical
best practices.
Medical testing and laboratory services - Remove an unnecessary
documentation requirement. Incorporate additional best practice standards.
Remove an unnecessary mandate, that will allow the patient and physician to
work together to determine the best course of action. Insert a new requirement
which will allow tracking of lab results.
Anesthesia Service - Incorporate additional best practice
standards. Add a documentation requirement.
Emergency Services - Align these provisions more precisely with
medical best practices. Remove an unnecessary provision that is not required
due to federal requirements.
Facility Design and Construction - Update the design and
construction requirements.
Documents Incorporated by Reference - Update those documents
incorporated by reference to reflect the most current publications.
Issues: The primary advantages of the regulatory action
to the public are increased health and safety protections at abortion
facilities. The primary disadvantage to the public associated with the
regulatory action is some abortion facilities may need to change some of their
current operating policies and procedures, which may cause a financial impact
on these facilities. The financial impact might be passed on to the facilities'
patients. The Department of Health does not foresee any additional
disadvantages to the public. The primary advantage to the agency and the
Commonwealth is the promotion of public health and safety. There are no
disadvantages associated with the proposed regulatory action in relation to the
agency or the Commonwealth.
Department of Planning and Budget's Economic Impact
Analysis:
Summary of the Proposed Amendments to Regulation. In this
action, the State Board of Health (Board) proposes to: 1) exempt existing
abortion facilities from meeting the Facilities Guidelines Institute (FGI)
Guidelines requirements, unless they build an addition or have a major
renovation, 2) require that new buildings, additions, and major renovations
meet the 2014 FGI Guidelines requirements (rather than the 2010 FGI Guidelines
requirements), 3) specify that abortion facilities that perform only medication
induced abortions meet general building requirements (instead of the special
building requirements for office-based procedures and operating rooms), 4)
amend requirements for when villi or fetal parts cannot be identified with
certainty in the tissue removed in the abortion, 5) no longer require that
abortion facilities have a written agreement with a licensed general hospital
regarding emergency treatment as this requirement is duplicative of federal law
and unnecessary, 6) no longer require abortion facilities to develop,
implement, and maintain policies and procedures for the screening of sexually
transmitted diseases as this service is not a part of abortion procedures, and
7) amend other language to be consistent with the Code or to make the
regulation more clear.
Estimated Economic Impact.
Exempting Existing Facilities. The current regulation requires
that abortion facilities, both existing and newly constructed, comply with
state and local codes, zoning, and building ordinances, the Virginia Uniform
Statewide Building Code, and specified sections of the 2010 Guidelines for
Design and Construction of Health Care Facilities of the Facilities Guidelines
Institute. In practice, 12 of the 16 abortion facilities operating in the
Commonwealth have been licensed with variances from meeting the FGI Guidelines
requirement. For the majority of facilities, complying with the requirement
would have cost hundreds of thousands of dollars.
The Board proposes to amend the requirement to apply to
"construction of new buildings and additions, or major renovations to
existing buildings for occupancy as an abortion facility that perform only
surgical abortions or a combination of surgical and medication induced
abortions." The amended language would exempt existing facilities from the
requirement, unless an addition or major renovation is built. Abortion
facilities would no longer need to apply for variances with this change.
According to the Department of Health, applying for a variance merely consists
of asking for a variance in writing (can be one paragraph or one sentence) when
applying for the yearly license renewal. So no longer needing to apply for a
variance saves only a negligible amount of time and effort for facilities. On the
other hand, the proposal to exempt existing facilities from the requirement
will likely reduce uncertainty for these facilities since the possibility of
having to meet the Guidelines requirement for their existing buildings (without
an addition or major renovation) due to the possibility of their variance
application disapproved will no longer apply.
2014 vs 2010 FGI Guidelines. The Board proposes to require that
new buildings, additions, and major renovations meet the 2014 FGI Guidelines1
requirements rather than the 2010 FGI Guidelines requirements. The Facility
Guidelines Institute published a study2 that estimates the change in
costs of applying the 2014 Guidelines rather than the 2010 Guidelines for
hospitals and outpatient facilities. The study breaks up hospitals and
outpatient facilities into five facility types, and lists the estimated
percentage cost increases for each category, as well as other across-the-board
changes that would reduce costs. Based upon the study's cost estimate for the
category that best fits abortion facilities and other factors that likely
reduce the estimated costs for abortion facilities,3 the proposal to
require that new buildings, additions, and major renovations meet the 2014 FGI
Guidelines requirements rather than the 2010 FGI Guidelines requirements would
on average increase net cost by less than two percent. The Board and the
architects and engineers associated with the Facility Guidelines Institute
believe that adopting the 2014 edition will increase patient and staff health
and safety. Thus, the proposed amendment will likely produce a net benefit.
Surgical vs Medication Induced. The Board proposes to specify
that abortion facilities that perform only medication induced abortions need
not be designed and constructed or renovated with the full requirements for
office-based procedures and operating rooms, but instead need only meet general
building requirements. The Board also proposes to add the following definition:
"Medication induced abortion means any abortion caused solely by the
administration of any medication or medications given to a woman in the first
trimester of pregnancy with the intent to produce abortion." There is one
current facility that falls into this category. If this facility were to
undertake a major renovation or build an addition, this proposed change would
potentially save the owners hundreds of thousands of dollars in construction
costs. The proposed amendment would also produce commensurate savings for the
construction of new facilities that perform only medication induced abortions,
but no surgical abortions.
When Villi or Fetal Parts Cannot Be Identified. Under both the
current regulation and the proposed regulation, all tissues removed resulting
from the abortion procedure must be examined to verify that villi or fetal
parts are present. Under the current regulation, if villi or fetal parts cannot
be identified with certainty, the tissue specimen must be sent for further
pathologic examination and the patient alerted to the possibility of an ectopic
pregnancy. The Board proposes to instead require that when villi or fetal parts
cannot be identified with certainty, the patient be notified that pregnancy
tissue was not identified and the possibility of ectopic pregnancy be explained
to the patient. In such cases, the patient is to be offered a pathologic
examination of the tissue including a disclosure of the cost; and should the
patient desire, the tissue specimen would be sent for further pathologic
examination. In essence, the proposed language enables the patient to make an
informed decision whether or not to order a pathologic examination of the
tissue, and to incur its associated cost. The proposed amendment likely
produces a net benefit since it allows the patient to make an informed decision,
rather than requiring that a potentially unwanted test be conducted.
Emergency Services and Screening for Sexually Transmitted
Diseases. The current regulation requires that "A written agreement shall
be executed with a licensed general hospital to ensure that any patient of the
abortion facility shall receive needed emergency treatment." The Board
determined that a written agreement is not necessary to ensure that any patient
of the abortion facility shall receive needed emergency treatment due to the federal
Emergency Medical Treatment and Labor Act. According to the Department of
Health, all facilities have thus far been able to obtain such written
agreements. Thus this proposed amendment will not significantly affect existing
abortion facilities. The proposed amendment would save the time involved for
obtaining such agreements for any potential future facilities.
The current regulation requires that "The abortion
facility shall develop, implement, and maintain policies and procedures for
screening of sexually transmitted diseases consistent with current guidelines
issued by the U.S. Centers for Disease Control and Prevention." Pursuant
to the recommendation of the Board's physician's regulatory advisory panel, the
Board proposes to eliminate this provision as it is unrelated to abortion
procedures. The Department of Health has accepted a statement indicating that
the facility does not have such procedures as fulfilling the requirement.4
Thus to the extent that abortion facilities have been aware of this, the
proposed amendment would not have a large impact.
Businesses and Entities Affected. The proposed amendments
pertain to the 16 licensed abortion facilities within the Commonwealth, as well
as any potential future abortion facilities. Six of the facilities qualify as
small businesses.5
Localities Particularly Affected. The 16 abortion facilities
operating in the Commonwealth are located in the following localities:
Alexandria (2), Blacksburg (1), Charlottesville (2), Fairfax (1), Falls Church
(1), Henrico (1), Newport News (1), Norfolk (1), Richmond (2), Roanoke (2), and
Virginia Beach (2).6
Projected Impact on Employment. The proposed amendments will
likely not significantly affect total employment.
Effects on the Use and Value of Private Property. Due to
significant reduction in associated cost, the proposal to specify that abortion
facilities that perform only medication induced abortions need not be designed
and constructed or renovated with the full requirements for office-based
procedures and operating rooms, may increase the likelihood that such
facilities are renovated or constructed.
Real Estate Development Costs. The proposal to require that new
buildings, additions, and major renovations meet the 2014 FGI Guidelines
requirements rather than the 2010 FGI Guidelines requirements would on average
increase net cost for the construction of new buildings, additions, and major
renovations of surgical abortion facilities by less than two percent.
The proposal to specify that abortion facilities that perform
only medication induced abortions need not be designed and constructed or
renovated with the full requirements for office-based procedures and operating
rooms would potentially save the owners hundreds of thousands of dollars in
construction 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 proposal to require that new
buildings, additions, and major renovations meet the 2014 FGI Guidelines
requirements rather than the 2010 FGI Guidelines requirements would on average
moderately increase net costs for small surgical abortion facilities that
undergo such construction projects.
The proposal to specify that abortion facilities that perform
only medication induced abortions need not be designed and constructed or
renovated with the full requirements for office-based procedures and operating
rooms, but instead need only meet general building requirements, would reduce
costs for small facilities that perform only medication induced abortions and
undergo building construction.
The proposals to no longer require that abortion facilities: a)
have a written agreement with a licensed general hospital to ensure that any
patient of the abortion facility shall receive needed emergency treatment, and
b) develop, implement, and maintain policies and procedures for screening of
sexually transmitted diseases, will moderately reduce costs for small abortion
facilities.
Alternative Method that Minimizes Adverse Impact. The proposal
to require that new buildings, additions, and major renovations meet the 2014
FGI Guidelines requirements rather than the 2010 FGI Guidelines requirements
will moderately increase costs in net for small abortion facilities that
undergo such projects. Not amending the regulation to include the 2014 edition
requirements would eliminate the moderate net cost increase, but would also
eliminate the likely increase in potential patient and staff health and safety.
Adverse Impacts:
Businesses. The proposal to require that new buildings,
additions, and major renovations meet the 2014 FGI Guidelines requirements
rather than the 2010 FGI Guidelines requirements would on average moderately
increase net costs for surgical abortion facilities that undergo such
construction projects.
Localities. The proposed amendments are unlikely to adversely
affect localities.
Other Entities. The proposed amendments are unlikely to
adversely affect other entities.
____________________________________
1The applicable 2014 edition is called Guidelines for
Design and Construction of Hospitals and Outpatient Facilities.
2Gormley T, Garland J, Jones W. "Estimated Cost of
Applying the 2014 vs. the 2010 FGI Guidelines for Design and Construction
Requirements to Hospitals and Outpatient Facilities."
3The facility type that best fits abortion facilities
includes dialysis centers. One of the items listed as contributing to cost
increases in this category is a new requirement for a soiled workroom in renal
dialysis centers. Since this does not apply to abortion facilities, the listed
estimate of a 2.68% cost increase for the category is likely too high for
abortion facilities. Combined with the across-the-board changes and a Board
proposal to exempt abortion facilities from a FGI Guideline procedure room size
requirement, the likely average net cost change for abortion facilities is less
than 2%
4Source: Virginia Department of Health
5Data source: Virginia Department of Health
6Ibid
Agency's Response to Economic Impact Analysis: The
Virginia Department of Health concurs with the economic impact analysis
conducted by the Department of Planning and Budget.
Summary:
The proposed amendments (i) clarify the requirements for
parental consent; (ii) add best practices for medical testing, laboratory
services, and anesthesia services; (iii) align the emergency services
requirements more specifically with medical best practices; (iv) update the
facility design and construction requirements; and (v) make minor technical
amendments. The proposed amendments are a result of the periodic review
conducted in accordance with Governor McAuliffe's Executive Directive 1 (2014).
Part I
Definitions and Requirements for Licensure
12VAC5-412-10. Definitions.
The following words and terms when used in this regulation
shall have the following meanings unless the context clearly indicates
otherwise:
"Abortion" means the use of an instrument,
medicine, drug, or other substance or device with the intent to terminate the
pregnancy of a woman, known to be pregnant, for reasons other than a live birth
or to remove a dead fetus. Spontaneous miscarriage is excluded
from this definition.
"Abortion facility" means a facility in which five
or more first trimester abortions per month are performed.
"Administrator" means the person appointed by the
governing body as having responsibility for the overall management of the
abortion facility. Job titles may include director, executive director, office
manager, or business manager.
"Commissioner" means the State Health Commissioner.
"Department" means the Virginia Department of
Health.
"First trimester" means the first 12 weeks from
conception based on an appropriate clinical estimate by a licensed physician
as determined in compliance with § 18.2-76 of the Code
of Virginia.
"Informed written consent" means the knowing and
voluntary written consent to abortion by a pregnant woman of any age in
accordance with § 18.2-76 of the Code of Virginia.
"Licensee" means the person, partnership,
corporation, association, organization, or professional entity who owns or on
whom rests the ultimate responsibility and authority for the conduct of the abortion facility.
"Medication induced abortion" means any abortion
caused solely by the administration of any medication or medications given to a
woman in the first trimester of pregnancy with the intent to produce abortion.
"Minor" means a patient under the age of 18.
"Patient" means any person seeking or obtaining
services at an abortion facility.
"Physician" means a person licensed to practice
medicine in Virginia.
"Spontaneous miscarriage" means the expulsion or
extraction of a product of human conception resulting in other than a live
birth and which is not an abortion.
"Surgical abortion" means any abortion caused by
any means other than solely by the administration of any medication or
medications given to a woman in the first trimester of pregnancy with the
intent to produce abortion.
"Trimester" means a 12-week period of pregnancy.
12VAC5-412-30. Classification. (Repealed.)
Abortion facilities shall be classified as a category of
hospital.
12VAC5-412-130. Violation of this chapter or applicable law;
denial, revocation, or suspension of license.
A. When the department determines that an abortion facility
is (i) in violation of any provision of Article 1 (§ 32.1-123 et seq.)
of Chapter 5 of Title 32.1 § 32.1-125.01, 32.1-125.4, 32.1-132,
32.1-135.2, or 32.1-137.01 of the Code of Virginia or of any applicable
regulation, or (ii) is permitting, aiding, or abetting the commission of
any illegal act in the abortion facility, the department may deny, suspend, or
revoke the license to operate an abortion facility in accordance with
§ 32.1-135 of the Code of Virginia.
B. If a license or certification is revoked as herein
provided, a new license or certification may be issued by the commissioner
after satisfactory evidence is submitted to him that the conditions upon which
revocation was based have been corrected and after proper inspection has been
made and compliance with all provisions of Article 1 of Chapter 5 of Title
32.1 § 32.1-125.01, 32.1-125.4, 32.1-132, 32.1-135.2, or
32.1-137.01 of the Code of Virginia and applicable state and federal law
and regulations hereunder has been obtained.
C. Suspension of a license shall in all cases be for an
indefinite time. The commissioner may restore a suspended license when he
determines that the conditions upon which suspension was based have been
corrected and that the interests of the public will not be jeopardized by
resumption of operation. No additional fee shall be required for restoring such
license.
D. The abortion facility has the right to contest the denial,
revocation, or suspension of a license in accordance with the provisions of the
Administrative Process Act (§ 2.2-4000 et seq. of the Code of Virginia).
Part IV
Patient Care Management
12VAC5-412-230. Patient services; patient counseling.
A. Abortions performed in abortion facilities shall be
performed only on patients who are within the first trimester of pregnancy based
on an appropriate clinical estimate by a licensed physician as
determined in compliance with § 18.2-76 of the Code of Virginia.
B. No person may perform an abortion upon an unemancipated
minor unless informed written consent is obtained from the minor and the
minor's parent, guardian, or other authorized person. The informed written
consent shall be notarized as required by § 16.1-241 of the Code of
Virginia. If the unemancipated minor elects not to seek the informed
written consent of an authorized person, a copy of the court order authorizing
the abortion entered pursuant to § 16.1-241 of the Code of Virginia shall
be obtained prior to the performance of the abortion.
C. A physician shall not perform an abortion without first
obtaining the informed written consent of the patient pursuant to the
provisions of § 18.2-76 of the Code of Virginia.
D. When abortions are being performed, a staff member
currently certified to perform cardiopulmonary resuscitation shall be available
on site for emergency care.
E. The abortion facility shall offer each patient seeking an
abortion, in a language or manner she understands, appropriate counseling and
instruction in the abortion procedure and shall develop, implement, and
maintain policies and procedures for the provision of or referral for
family planning and post-abortion counseling services to its
patients.
F. There shall be an organized discharge planning process
that includes an evaluation of the patient's capacity for self-care and an
assessment of a patient's safety for discharge and discharge instructions
for patients to include instructions to call or return if signs of infection
develop.
12VAC5-412-240. Medical testing and laboratory services.
A. Prior to the initiation of any abortion, a medical history
and physical examination, including a confirmation of pregnancy, and completion
of all the requirements of informed written consent pursuant to § 18.2-76 of
the Code of Virginia, shall be completed for each patient.
1. Use of any additional medical testing shall be based on
an assessment of patient risk. The clinical criteria for such additional
testing and the actions to be taken if abnormal results are found shall be
documented. Medical testing shall include a recognized method to confirm
pregnancy and determination or documentation of Rh factor.
2. Medical testing shall include a recognized method to
confirm pregnancy and determination or documentation of Rh factor. Use
of any additional medical testing shall be based on an assessment of patient
risk.
3. The abortion facility shall develop, implement, and
maintain policies and procedures for screening of sexually transmitted diseases
consistent with current guidelines issued by the U.S. Centers for Disease
Control and Prevention. The policies and procedures shall address appropriate
responses to a positive screening test.
4. 3. A written report of each laboratory test
and examination shall be a part of the patient's record.
B. Laboratory services shall be provided on site or through
arrangement with a laboratory certified to provide the required procedures
under the Clinical Laboratory Improvement Amendments of 1988 (CLIA-88) (42 CFR
Part 493).
1. Facilities for collecting specimens shall be available on
site.
2. If laboratory services are provided on site they shall be
directed by a person who qualifies as a director under CLIA-88 and shall be
performed in compliance with CLIA-88 standards.
3. All laboratory supplies shall be monitored for expiration
dates, if applicable, and disposed of properly.
C. All tissues removed resulting from the abortion procedure
shall be examined to verify that villi or fetal parts are present if;.
If villi or fetal parts cannot be identified with certainty, the patient
shall be notified that pregnancy tissue was not identified and the possibility
of ectopic pregnancy shall be explained to the patient. In such cases, the
patient shall be offered a pathologic examination of the tissue including a
disclosure of the cost and should the patient desire, the tissue specimen
shall be sent for further pathologic examination and the patient alerted to
the possibility of an ectopic pregnancy, and referred appropriately. The
facility shall track and log any specimens sent for further pathologic
examination.
D. All tissues removed resulting from the abortion
procedure shall be managed in accordance with requirements for medical waste
pursuant to the Regulated Medical Waste Management Regulations (9VAC20-120).
12VAC5-412-250. Anesthesia service.
A. The anesthesia service shall comply with the office-based
anesthesia provisions of the Regulations Governing the Practice of Medicine,
Osteopathic Medicine, Podiatry, and Chiropractic (18VAC85-20-310 et seq.).
B. The anesthesia service shall be directed by and under the
supervision of a physician licensed in Virginia.
C. When moderate sedation or conscious sedation is
administered, the licensed health care practitioner who administers the
anesthesia shall routinely monitor the patient according to procedures
consistent with such administration. The administration of sedation and
monitoring of the patient shall be documented in the patient's medical record.
D. An abortion facility administering moderate
sedation/conscious sedation shall maintain the following equipment, supplies,
and pharmacological agents as required by 18VAC85-20-360 B:
1. Appropriate equipment to manage airways;
2. Drugs and equipment to treat shock and anaphylactic
reactions;
3. Precordial stethoscope;
4. Pulse oximeter with appropriate alarms or an equivalent
method of measuring oxygen saturation;
5. Continuous electrocardiograph;
6. Devices for measuring blood pressure, heart rate, and
respiratory rate;
7. Defibrillator; and
8. Accepted method of identifying and preventing the interchangeability
of gases.
E. Elective general anesthesia shall not be used.
F. If deep sedation or a major conductive block is
administered or if general anesthesia is administered in an emergent situation,
the licensed health care practitioner who administers the anesthesia service
shall remain present and available in the facility to monitor the patient until
the patient meets the discharge criteria.
G. In addition to the requirements of subsection D of this
section, an abortion facility administering deep sedation or a major conductive
block, or administering general anesthesia in an emergent situation, shall
maintain the following equipment, supplies, and pharmacological agents as
required by 18VAC85-20-360 C:
1. Drugs to treat malignant hyperthermia, when triggering
agents are used;
2. Peripheral nerve stimulator, if a muscle relaxant is used;
and
3. If using an anesthesia machine, the following shall be
included:
a. End-tidal carbon dioxide monitor (capnograph);
b. In-circuit oxygen analyzer designed to monitor oxygen
concentration within breathing circuit by displaying oxygen percent of the
total respiratory mixture;
c. Oxygen failure-protection devices (fail-safe system) that
have the capacity to announce a reduction in oxygen pressure and, at lower
levels of oxygen pressure, to discontinue other gases when the pressure of the
supply of oxygen is reduced;
d. Vaporizer exclusion (interlock) system, which ensures that
only one vaporizer, and therefore only a single anesthetic agent can be actualized
on any anesthesia machine at one time;
e. Pressure-compensated anesthesia vaporizers, designed to
administer a constant nonpulsatile output, which shall not be placed in the
circuit downstream of the oxygen flush valve;
f. Flow meters and controllers, which can accurately gauge
concentration of oxygen relative to the anesthetic agent being administered and
prevent oxygen mixtures of less than 21% from being administered;
g. Alarm systems for high (disconnect), low (subatmospheric),
and minimum ventilatory pressures in the breathing circuit for each patient
under general anesthesia; and
h. A gas evacuation system.
H. The abortion facility shall develop, implement, and
maintain policies and procedures outlining criteria for discharge from
anesthesia care. Such criteria shall include stable vital signs, responsiveness
and orientation, ability to move voluntarily, controlled pain, and minimal
nausea and vomiting. Discharge from anesthesia care is the responsibility of
the health care practitioner providing the anesthesia care and shall occur only
when the patient has met specific physician-defined criteria, and those
criteria have been documented within the patient's medical record.
12VAC5-412-290. Emergency services.
A. An abortion facility shall provide ongoing urgent or
emergent care and maintain on the premises adequate monitoring equipment,
suction apparatus, oxygen, and related items for resuscitation and control of
hemorrhage and other complications.
B. An abortion facility that performs abortions using
intravenous sedation shall provide equipment and services to render emergency
resuscitative and life-support procedures pending transfer of the patient to a
hospital. Such medical equipment and services shall be consistent with the
current edition of the American Heart Association's Guidelines for Advanced
Cardiopulmonary Resuscitation and Emergency Cardiovascular Life
Support Care.
C. A written agreement shall be executed with a licensed
general hospital to ensure that any patient of the abortion facility shall
receive needed emergency treatment. The agreement shall be with a licensed
general hospital capable of providing full surgical, anesthesia, clinical
laboratory, and diagnostic radiology service on 30 minutes notice and which has
a physician in the hospital and available for emergency service at all times.
When emergency transfer is necessary, the responsible physician at the abortion
facility must provide direct communication to the emergency department staff
appropriate receiving facility staff regarding the status of the
patient, the procedure details, and the suspected complication. All patients
must be provided with contact information for a representative of the abortion
facility, so that an emergency department physician or treating provider may
make contact with a provider of the facility if late complications arise.
Part VII
Design and Construction
12VAC5-412-370. Local and state codes and standards.
Abortion facilities A. All construction of new
buildings and additions or major renovations to existing buildings for
occupancy as an abortion facility shall comply with conform to
state and local codes, and zoning, and building ordinances
and the Virginia Uniform Statewide Building Code (13VAC5-63). In addition,
abortion facilities All construction of new buildings and additions or
major renovations to existing buildings for occupancy as an abortion facility
that perform only surgical abortions or a combination of surgical and
medication induced abortions shall comply be designed and constructed
consistent with Part 1 and sections 3.1-1 through 3.1-8 and
section 3.7 section 3.8 of Part 3 of the 2010 Guidelines for
Design and Construction of Health Care Hospitals and Outpatient
Facilities of the, 2014 edition, The Facilities Guidelines Institute
(2014 guidelines), which shall take precedence over the Virginia
Uniform Statewide Building Code pursuant to § 32.1-127.001 of the Code
of Virginia. Abortion facilities that perform only medication induced
abortions shall be designed and constructed consistent with sections 1.1, 1.3,
and 1.4 of Part 1 of the 2014 guidelines.
Entities operating as of the effective date of this
chapter as identified by the department through submission of Reports of
Induced Termination of Pregnancy pursuant to 12VAC5-550-120 or other means and
that are now subject to licensure may be licensed in their current buildings if
such entities submit a plan with the application for licensure that will bring
them into full compliance with this provision within two years from the date of
licensure.
Abortion procedures may take place in a procedure room, as
detailed in section 3.8-3.1 of Part 3 of the 2014 guidelines, except that
minimum square footage requirements for procedure rooms used for the provision
of surgical abortion do not need to be greater than 120 square feet, with a
minimum room dimension of 10 feet and a minimum clear dimension of three feet
at each side and at the foot of the bed. Rooms designed in accordance with
section 3.8-3.2 of Part 3 of the 2014 guidelines are not required
for abortion facilities. Section 3.7-3.6.13.1(2) of Part 3 of the 2014
guidelines shall not apply to facilities that do not have a room designed in
accordance with section 3.8-3.2.
Architectural drawings and specifications for all new
construction or for additions, alterations, or renovations to any existing
building shall be dated, stamped with professional seal, and signed by the
architect. The architect shall certify that the drawings and specifications
were prepared to conform to the Virginia Uniform Statewide Building Code
(13VAC5-63) and be consistent with the applicable sections of the 2014
guidelines. The certification shall be forwarded to the Office of Licensure and
Certification of the Virginia Department of Health.
B. In order to determine whether the abortion facility
facility's design and construction is in compliance consistent
with this provision the applicable sections of the 2014 guidelines,
the commissioner may obtain additional information from the facility or its
architect concerning the design and construction of the facility.
DOCUMENTS INCORPORATED BY REFERENCE (12VAC5-412)
Guidelines for Design and Construction of Health Care Hospitals
and Outpatient Facilities, 2010 Edition 2014 edition, Part
1 and Sections 3.1-1 through 3.1-8 and 3.7 of Part 3, The Facilities
Guidelines Institute (formerly of the American Institute of Architects),
Washington, D.C. (http://www.fgiguidelines.org)
Guidelines for Cardiopulmonary Resuscitation and Emergency
Cardiovascular Care. Circulation. November 2, 2010, Volume 122, Issue 18 Suppl
3, American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231-4596 (http://circ.ahajournals.org/content/vol122/18_suppl_3/).
Sexually Transmitted Diseases Treatment Guidelines, 2010,
Centers for Disease Control and Prevention, U.S. Department of Health and Human
Services
Guide to Infection Prevention for Outpatient Settings:
Minimum Expectations for Safe Care, Centers for Disease Control and Prevention,
U.S. Department of Health and Human Services
(http://www.cdc.gov/HAI/prevent/prevent_pubs.html)
Guide
to Infection Prevention for Outpatient Settings: Minimum Expectations for Safe
Care, version 2.2, November 2015, Centers for Disease Control and Prevention,
U.S. Department of Health and Human Services (http://www.cdc.gov/HAI/settings/outpatient/outpatient-care-guidelines.html)
Standards for Ambulatory Care, Rights and Responsibilities
of the Individual, 2011, 2015 Standards for Ambulatory Care, The
Joint Commission, 1515 W. 22nd Street, Suite 1300W, Oak Brook, IL 60523,
telephone 1-877-223-2866 1-770-238-0454, email jcrcustomerservice@pbd.com.
Bloodborne Pathogens - OSHA's Bloodborne Pathogens
Standard, OSHA Fact Sheet and Quick Reference Guide, 2011 U.S. Occupational
Safety and Health Administration.
VA.R. Doc. No. R15-4258; Filed April 12, 2016, 5:24 p.m.
TITLE 23. TAXATION
DEPARTMENT OF TAXATION
Fast-Track Regulation
Title of Regulation: 23VAC10-60. Virginia Egg Excise
Tax (repealing 23VAC10-60-40, 23VAC10-60-50).
Statutory Authority: § 58.1-203 of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: July 1, 2016.
Effective Date: July 18, 2016.
Agency Contact: Joseph E. Mayer, Lead Policy Analyst,
Department of Taxation, P.O. Box 27185, Richmond, VA 23261-7185, telephone
(804) 371-2299, FAX (804) 371-2355, or email joseph.mayer@tax.virginia.gov.
Basis: Section 58.1-203 of the Code of Virginia
authorizes the Tax Commissioner to issue regulations relating to the
interpretation and enforcement of the laws governing taxes administered by the
Department of Taxation. Section 3.2-1607 of the Code of Virginia authorizes the
Tax Commissioner to administer the egg excise tax.
Purpose: As a result of a periodic review of the egg
excise tax regulation (23VAC10-60) initiated by the Department of Taxation on
April 28, 2015, and completed June 6, 2015, the Department of Taxation has
determined that the regulation should be repealed because it provides no
guidance beyond the plain meaning of the statutes to which it applies and is
not necessary to protect the public health, safety, or welfare. A regulation
that is not necessary to interpret the law or to protect the public health,
safety, or welfare violates the general principles set forth in Governor
McAuliffe's Executive Order 17 signed June 30, 2014.
Repeal of the regulation does not reflect any change in current
tax policy. Repeal of the regulation will have no impact on the administration
of the egg excise tax.
Rationale for Using Fast-Track Rulemaking Process: The
repeal of the egg excise tax regulation is expected to be noncontroversial
because the regulation provides no guidance beyond the plain meaning of the
statutes to which it applies. No comments were received during the periodic
review of the regulation.
Substance: This action will repeal the egg excise tax
regulation. The egg excise tax is levied on eggs, in both shell and liquid
form, purchased or sold for use or consumption in the Commonwealth. The tax is
remitted monthly and the revenues deposited into the Egg Fund. The Egg Board
uses these funds to provide for programs of research, education, publicity, advertising,
and other promotion of eggs.
Because the regulation provides no guidance beyond the plain
meaning of the statutes to which it applies, repeal of the regulation does not
reflect any change in current tax policy. Repeal of the regulation will have no
impact on the administration of the egg excise tax.
Issues: As the regulation provides no additional
guidance to statutes that are clear and unambiguous, it is unnecessary.
Accordingly, its repeal 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 Taxation (Department) proposes to repeal this regulation.
Result of Analysis. The repeal of this regulation will have no
impact in that all sections are repetitive of statutes.
Estimated Economic Impact. The text in this regulation is
repetitive of language in the following sections of the Code of Virginia: §
3.2-1600, § 3.2-1607, and § 3.2-1608. Repealing the regulation will have
no impact in that all sections are repetitive of statutes.
Businesses and Entities Affected. The regulation and statutes
pertain to the 901 registered egg handlers in the Commonwealth. Code
of Virginia § 3.2-1600 defines a "handler" as "any person
who operates a grading station, a packer, distributor, or other person who
purchases, sells, or handles eggs that are used at the wholesale level for
consumption in Virginia or, a farmer who packs, processes, or otherwise
performs the functions of a handler."
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.
________________________
1 Data source: Department of Taxation
Agency's Response to Economic Impact Analysis: The
Department of Taxation agrees with the Department of Planning and Budget's
economic impact analysis.
Summary:
The Department of Taxation determined that the regulation provides
no guidance beyond the plain meaning of the statutes to which it applies and is
not necessary to protect the public health, safety, or welfare. Therefore, the
regulation is repealed. The repeal of the regulation does not reflect a change
in current tax policy and has no impact on the administration of the egg excise
tax.
VA.R. Doc. No. R16-4556; Filed April 5, 2016, 11:57 a.m.
TITLE 23. TAXATION
DEPARTMENT OF TAXATION
Fast-Track Regulation
Title of Regulation: 23VAC10-65. Virginia Peanut
Excise Tax (repealing 23VAC10-65-40).
Statutory Authority: § 58.1-203 of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: July 1, 2016.
Effective Date: July 18, 2016.
Agency Contact: Joseph E. Mayer, Lead Policy Analyst,
Department of Taxation, P.O. Box 27185, Richmond, VA 23261-7185, telephone
(804) 371-2299, FAX (804) 371-2355, or email joseph.mayer@tax.virginia.gov.
Basis: Section 58.1-203 of the Code of Virginia
authorizes the Tax Commissioner to issue regulations relating to the
interpretation and enforcement of the laws governing taxes administered by the
Department of Taxation. Section 3.2-1907 of the Code of Virginia authorizes the
Tax Commissioner to administer the peanut excise tax.
Purpose: As a result of a periodic review of the peanut
excise tax regulation (23VAC10-65) initiated by the Department of Taxation on
April 28, 2015, and completed June 6, 2015, the Department of Taxation has
determined that the regulation should be repealed because it provides no
guidance beyond the plain meaning of the statutes to which it applies and it is
not necessary to protect the public health, safety, or welfare. A regulation
that is not necessary to interpret the law or to protect the public health,
safety, or welfare violates the general principles set forth in Governor
McAuliffe's Executive Order 17 signed June 30, 2014.
Repeal of the regulation does not reflect any change in current
tax policy. Repeal of the regulation will have no impact on the administration
of the peanut excise tax.
Rationale for Using Fast-Track Rulemaking Process: The
Department of Taxation is using the fast-track rulemaking process because the
repeal of the peanut excise tax regulation is expected to be noncontroversial
because the regulation provides no guidance beyond the plain meaning of the
statutes to which it applies. No comments were received during the periodic
review of the regulation.
Substance: This action will repeal the peanut excise tax
regulation. The peanut excise tax is levied on peanuts grown in and sold in the
Commonwealth for processing. The tax is remitted semiannually and the revenues
deposited into the Peanut Fund. The Peanut Board uses these funds to plan and
conduct campaigns for education, advertising, publicity, sales promotion, and
research for Virginia peanuts.
Because the regulation provides no guidance beyond the plain
meaning of the statutes to which it applies, repeal of the regulation does not
reflect any change in current tax policy. Repeal of the regulation will have no
impact on the administration of the peanut excise tax.
Issues: As the regulation provides no additional
guidance to statutes that are clear and unambiguous, it is unnecessary.
Accordingly, its repeal 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 Taxation (Department) proposes to repeal this regulation.
Result of Analysis. The repeal of this regulation will have no
impact in that all sections are either obsolete or repetitive of statutes.
Estimated Economic Impact. The text in this regulation is
either obsolete or repetitive of language in Code of Virginia: § 3.2-1908.
Repealing the regulation will therefore have no impact.
Businesses and Entities Affected. The regulation and statutes
pertain to the 111 peanut processors in the Commonwealth.
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.
_________________________
1 Data source: Department of Taxation
Agency's Response to Economic Impact Analysis: The
Department of Taxation agrees with the Department of Planning and Budget's
economic impact analysis.
Summary:
The Department of Taxation determined that the regulation
provides no guidance beyond the plain meaning of the statutes to which it
applies and is not necessary to protect the public health, safety, or welfare.
Therefore, the regulation is repealed. The repeal of the regulation does not
reflect a change in current tax policy and has no impact on the administration
of the peanut excise tax.
VA.R. Doc. No. R16-4557; Filed April 5, 2016, 12:00 p.m.
TITLE 23. TAXATION
DEPARTMENT OF TAXATION
Fast-Track Regulation
Title of Regulation: 23VAC10-75. Virginia Soybean
Excise Tax Regulations (repealing 23VAC10-75-20).
Statutory Authority: § 58.1-203 of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: July 1, 2016.
Effective Date: July 18, 2016.
Agency Contact: Joseph E. Mayer, Lead Policy Analyst,
Department of Taxation, P.O. Box 27185, Richmond, VA 23261-7185, telephone
(804) 371-2299, FAX (804) 371-2355, or email joseph.mayer@tax.virginia.gov.
Basis: Section 58.1-203 of the Code of Virginia
authorizes the Tax Commissioner to issue regulations relating to the
interpretation and enforcement of the laws governing taxes administered by the
Department of Taxation. Section 3.2-2312 of the Code of Virginia authorizes the
Tax Commissioner to administer the soybean excise tax.
Purpose: As a result of a periodic review of the
Virginia Soybean Excise Tax Regulations (23VAC10-75) initiated by the
Department of Taxation on April 28, 2015, and completed June 6, 2015, the
Department of Taxation has determined that the regulation should be repealed
because it provides no guidance beyond the plain meaning of the statutes to
which it applies and is not necessary to protect the public health, safety, or
welfare. A regulation that is not necessary to interpret the law or to protect
the public health, safety, or welfare violates the general principles set forth
in Governor McAuliffe's Executive Order 17 signed June 30, 2014.
Repeal of the regulation does not reflect any change in current
tax policy. Repeal of the regulation will have no impact on the administration
of the soybean excise tax.
Rationale for Using Fast-Track Rulemaking Process: The
repeal of the Virginia Soybean Excise Tax Regulations is expected to be
noncontroversial because the regulation provides no guidance beyond the plain
meaning of the statutes to which it applies. No comments were received during
the periodic review of the regulation.
Substance: This action will repeal the Virginia Soybean
Excise Tax Regulations. The soybean excise tax is levied on soybeans purchased
in the Commonwealth. The tax is remitted quarterly and the revenues deposited
into the Soybean Fund. The Soybean Board uses these funds to provide for
programs of research, education, publicity, and the promotion of the sale and
use of soybeans.
Because the regulation provides no guidance beyond the plain
meaning of the statutes to which it applies, repeal of the regulation does not
reflect any change in current tax policy. Repeal of the regulation will have no
impact on the administration of the soybean excise tax.
Issues: As the regulation provides no additional
guidance to statutes that are clear and unambiguous, it is unnecessary.
Accordingly, its repeal 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 Taxation (Department) proposes to repeal this regulation.
Result of Analysis. The repeal of this regulation will have no
impact in that all sections are either obsolete or repetitive of statutes.
Estimated Economic Impact. The text in this regulation is
either obsolete or repetitive of language in Code of Virginia: § 3.2-2313.
Repealing the regulation will therefore have no impact.
Businesses and Entities Affected. The regulation and statutes
pertain to the 371 soybean handlers in the Commonwealth. Code of
Virginia § 3.2-2300 defines a "handler" as "any processor,
dealer, shipper, exporter, or any other business entity that purchases soybeans
from a producer."
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.
_________________________
1 Data source: Department of Taxation
Agency's Response to Economic Impact Analysis: The
Department of Taxation agrees with the Department of Planning and Budget's
economic impact analysis.
Summary:
The Department of Taxation determined that the regulation
provides no guidance beyond the plain meaning of the statutes to which it
applies and is not necessary to protect the public health, safety, or welfare.
Therefore, the regulation is repealed. The repeal of the regulation does not
reflect a change in current tax policy and has no impact on the administration
of the soybean excise tax.
VA.R. Doc. No. R16-4558; Filed April 5, 2016, 12:03 p.m.
TITLE 23. TAXATION
DEPARTMENT OF TAXATION
Fast-Track Regulation
Title of Regulation: 23VAC10-400. Writ Taxes
Regulations (repealing 23VAC10-400-10).
Statutory Authority: § 58.1-203 of the Code of Virginia.
Public Hearing Information: No public hearings are
scheduled.
Public Comment Deadline: July 1, 2016.
Effective Date: July 18, 2016.
Agency Contact: Joseph E. Mayer, Lead Policy Analyst,
Department of Taxation, P.O. Box 27185, Richmond, VA 23261-7185, telephone
(804) 371-2299, FAX (804) 371-2355, or email joseph.mayer@tax.virginia.gov.
Basis: Section 58.1-203 of the Code of Virginia
authorizes the Tax Commissioner to issue regulations relating to the
interpretation and enforcement of the laws governing taxes administered by the
Department of Taxation. Sections 58.1-1727, 58.1-1728, and 58.1-1729 of the
Code of Virginia impose writ taxes.
Purpose: As a result of a periodic review of the Writ
Taxes Regulations (23VAC10-400) initiated by the Department of Taxation on
April 28, 2015, and completed June 6, 2015, the Department of Taxation has
determined that the regulation should be repealed because it provides no
guidance beyond the plain meaning of the statutes to which it applies and is
not necessary to protect the public health, safety, or welfare. A regulation
that is not necessary to interpret the law or to protect the public health,
safety, or welfare violates the general principles set forth in Governor
McAuliffe's Executive Order 17 signed June 30, 2014.
Repeal of the regulation does not reflect any change in
current tax policy. Repeal of the regulation will have no impact on the
administration of the writ taxes.
Rationale for Using Fast-Track Rulemaking Process: The
repeal of the Writ Taxes Regulations is expected to be noncontroversial because
the regulation provides no guidance beyond the plain meaning of the statutes to
which it applies. No comments were received during the periodic review of the
regulation.
Substance: This action will repeal the Writ Taxes
Regulations. A writ tax is levied on (i) any original suit that is commenced in
a court of record, (ii) every case of removal or appeal of a cause from a
district court to a court of record, (iii) every appeal from the decision of
the board of supervisors or other governing body of a county to a court of
record, (iv) every attachment returnable to a court of record, and (v) every
writ of mandamus sued out of any court except the Supreme Court of Virginia.
The taxes are paid to the clerk of court wherein the suit or other judicial
proceeding is commenced.
Because the regulation provides no guidance beyond the plain
meaning of the statutes to which it applies, repeal of the regulation does not
reflect any change in current tax policy. Repeal of the regulation will have no
impact on the administration of the writ taxes.
Issues: As the regulation provides no additional
guidance to statutes that are clear and unambiguous, it is unnecessary.
Accordingly, its repeal 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.
The Department of Planning and Budget's Economic Impact
Analysis:
Summary of the Proposed Amendments to Regulation. The
Department of Taxation (Department) proposes to repeal this regulation.
Result of Analysis. The repeal of this regulation will have no
impact in that all sections are either obsolete, or repetitive of either the
Constitution of Virginia or the Code of Virginia.
Estimated Economic Impact. The text in this regulation is
either obsolete, repetitive of language in the Constitution of Virginia
(Article X, Section 6(a)), or repetitive of the Code of Virginia
(§ 17.1-606). Thus, repealing the regulation will have no impact.
Businesses and Entities Affected. The regulation, relevant
portion of the state constitution, and statute all pertain to exemptions to
taxation on legal proceedings. The exemptions apply to the indigent and
political subdivisions in particular.
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 Department
of Taxation agrees with the Department of Planning and Budget's economic impact
analysis.
Summary:
The Department of Taxation determined that the regulation
provides no guidance beyond the plain meaning of the statutes to which it
applies and is not necessary to protect the public health, safety, or welfare.
Therefore, the regulation is repealed. The repeal of the regulation does not
reflect a change in current tax policy and has no impact on the administration
of the writ taxes.
VA.R. Doc. No. R16-4559; Filed April 5, 2016, 12:05 p.m.
Documents of the Virginia Economic Development Partnership
(VEDP) are available using the links below, which will link the user to the
guidance document on VEDP's Ally Information Exchange website at http://virginiaallies.org.
Questions regarding these documents may be directed to
Alexander R. Thorup, Manager, Legislation and Policy, Virginia Economic
Development Partnership, 901 East Byrd Street, P.O. Box 798, Richmond, VA
23218-0798, telephone (804) 545-5600.