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
 
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*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.