Public Meeting: Preliminary Regulatory Determinations for the Third Contaminant Candidate List (CCL 3), 31271-31272 [2011-13404]
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Federal Register / Vol. 76, No. 104 / Tuesday, May 31, 2011 / Proposed Rules
consensus standards’’ (VCS) if available
and applicable when developing
programs and policies unless doing so
would be inconsistent with applicable
law or otherwise impractical.
The EPA believes that VCS are
inapplicable to this action. Today’s
action does not require the public to
perform activities conducive to the use
of VCS.
List of Subjects in 40 CFR Part 52
Air pollution control, Environmental
protection, Intergovernmental relations,
Nitrogen dioxide, Ozone, Particulate
matter, Reporting and recordkeeping
requirements, Volatile organic
compounds.
Dated: May 20, 2011.
Keith Takata,
Acting Regional Administrator, Region IX.
Title 40, chapter I, of the Code of
Federal Regulations is proposed to be
amended as follows:
PART 52—[AMENDED]
§ 52.270
quality.
1. The authority citation for part 52
continues to read as follows:
Subpart F—California
2. Section 52.233 is amended by
adding paragraph (h) to read as follows:
§ 52.233 Review of new sources and
modifications.
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(h) Regulation for review of major
stationary sources and major
modifications for nitrogen oxides. (1)
Upon the effective date of this
regulation, the requirements of this
paragraph are applicable to any source
under the jurisdiction of the APCDs
listed below that is a major stationary
source or major modification for
nitrogen oxides in a ‘‘serious’’ ozone
nonattainment area under 40 CFR part
51, Appendix S, and that is not
otherwise subject to new source review
under the applicable SIP for the area.
(i) Feather River AQMD.
(ii) Placer County APCD.
(iii) Sacramento Metropolitan AQMD.
(2) Except for a major stationary
source that is subject to new source
review under the applicable SIP for the
area, no owner or operator shall
commence construction of a new
stationary source that emits or has the
potential to emit 50 tons per year or
more of nitrogen oxides, without first
obtaining approval from the
Administrator.
(3) Except for a major modification
that is subject to new source review
under the applicable SIP for the area, no
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Significant deterioration of air
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Authority: 42 U.S.C. 7401 et seq.
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owner or operator shall commence
construction of a modification to an
existing stationary source that results in
a net emissions increase of 25 tons per
year or more of nitrogen oxides, without
first obtaining approval from the
Administrator.
(4) For any major stationary source or
major modification subject to this
paragraph in accordance with the
emission thresholds identified in
paragraphs (h)(2) and (3) of this section,
the Administrator shall approve the
construction of such source or
modification if the owner or operator
demonstrates that construction of such
source or modification satisfies the
requirements of Sacramento
Metropolitan AQMD Rule 202, as
approved on June 19, 1985 (50 FR
25417).
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3. Section 52.270 is amended by
adding paragraphs (b)(2)(iv), (b)(3)(iv),
and (b)(4)(iv) to read as follows:
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(b) * * *
(2) * * *
(iv) Those projects which are major
stationary sources or major
modifications for nitrogen oxides as
precursors to ozone under § 52.21.
(3) * * *
(iv) Those projects which are major
stationary sources or major
modifications for nitrogen oxides as
precursors to ozone under § 52.21.
(4) * * *
(iv) Those projects which are major
stationary sources or major
modifications for nitrogen oxides as
precursors to ozone under § 52.21.
[FR Doc. 2011–13397 Filed 5–27–11; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 141
[FRL–9313–3]
Public Meeting: Preliminary Regulatory
Determinations for the Third
Contaminant Candidate List (CCL 3)
Environmental Protection
Agency (EPA).
ACTION: Announcement of meeting.
AGENCY:
The 1996 Safe Drinking Water
Act Amendments require the EPA to
determine every five years, whether to
regulate at least five contaminants from
the current Contaminant Candidate List
(CCL) with a national primary drinking
SUMMARY:
PO 00000
Frm 00010
Fmt 4702
Sfmt 4702
31271
water regulation. The process of making
decisions about whether to regulate any
of the unregulated contaminants on the
CCL is called Regulatory
Determinations. On October 8, 2009,
EPA published the third Contaminant
Candidate List (CCL 3) containing 116
unregulated contaminants. The Agency
is currently in the preliminary process
of deciding whether to regulate at least
five CCL 3 contaminants (i.e.,
Regulatory Determinations 3). The
purpose of this notice is to announce
that EPA will be hosting a public
stakeholder meeting on June 16, 2011,
from 1 p.m. to 5 p.m., to discuss and
obtain input on EPA’s process for
Regulatory Determination 3 along with
the contaminants and the technical
information that the Agency is
considering. EPA expects to publish the
preliminary regulatory determinations
for at least five CCL 3 contaminants in
mid-2012 and final regulatory
determinations by August 2013.
DATES: The public meeting will be held
in the Washington, DC metropolitan
area on Thursday, June 16, 2011, from
1 p.m. to 5 p.m., Eastern Daylight
Savings Time. Participants will be
notified of the specific meeting room
upon confirmation of registration.
FOR FURTHER INFORMATION CONTACT: For
technical inquiries regarding EPA’s
Regulatory Determinations for
contaminants on CCL 3 contact: Mr.
Zeno Bain at (202) 564–5970 or by email: bain.zeno@epa.gov. For additional
information about the drinking water
Contaminant Candidate List and the
Regulatory Determinations process,
please visit: https://water.epa.gov/
scitech/drinkingwater/dws/ccl/
index.cfm. Additional information on
these and other EPA activities under the
Safe Drinking Water Act is also
available at the Safe Drinking Water
Hotline at (800) 426–4791.
SUPPLEMENTARY INFORMATION:
Registration: Individuals planning to
attend the Stakeholder Meeting must
register for the meeting by contacting
Melissa Simic at (202) 564–7722 or by
sending an e-mail to
simic.melissa@epa.gov no later than
Wednesday, June 8, 2011. There is no
charge for attending the meeting but
seats are limited, so register as soon as
possible. Please note that attendees will
be required to pass through security
checks at the front desk and obtain a
visitor’s badge. Pre-registration for this
meeting will help us facilitate your
check-in.
Special Accommodations: The
meeting will be held in a building
which is accessible to persons using
wheel chairs or scooters. For
E:\FR\FM\31MYP1.SGM
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31272
Federal Register / Vol. 76, No. 104 / Tuesday, May 31, 2011 / Proposed Rules
information on access or
accommodations for individuals with
disabilities, please contact Melissa
Simic at (202) 564–7722 or by e-mail at
simic.melissa@epa.gov. Please allow at
least five business days prior to the
meeting to give EPA time to process
your request.
Dated: May 24, 2011.
Eric M. Bissonette,
Acting Director, Office of Ground Water and
Drinking Water.
[FR Doc. 2011–13404 Filed 5–27–11; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
45 CFR Part 170
RIN 0991–AB77
Permanent Certification Program for
Health Information Technology;
Revisions to ONC-Approved
Accreditor Processes
Office of the National
Coordinator for Health Information
Technology (ONC), Department of
Health and Human Services.
ACTION: Proposed rule.
AGENCY:
Under the authority granted
to the National Coordinator for Health
Information Technology (the National
Coordinator) by section 3001(c)(5) of the
Public Health Service Act (PHSA) as
added by the Health Information
Technology for Economic and Clinical
Health (HITECH) Act, this rule proposes
a process for addressing instances where
the ONC-Approved Accreditor (ONC–
AA) engages in improper conduct or
does not perform its responsibilities
under the permanent certification
program. This rule also proposes to
address the status of ONC-Authorized
Certification Bodies (ONC–ACBs) in
instances where there may be a change
in the accreditation organization serving
as the ONC–AA and clarifies the
responsibilities of the new ONC–AA.
DATES: To be assured consideration,
written or electronic comments must be
received at one of the addresses
provided below, no later than 5 p.m. on
August 1, 2011.
ADDRESSES: Because of staff and
resource limitations, we cannot accept
comments by facsimile (FAX)
transmission. You may submit
comments, identified by RIN 0991–
AB77, by any of the following methods
(please do not submit duplicate
comments).
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SUMMARY:
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• Federal eRulemaking Portal: Follow
the instructions for submitting
comments. Attachments should be in
Microsoft Word or Excel, Adobe PDF;
however, we prefer Microsoft Word.
https://www.regulations.gov.
• Regular, Express, or Overnight Mail:
Department of Health and Human
Services, Office of the National
Coordinator for Health Information
Technology, Attention: Revisions to
ONC–AA Processes Proposed Rule,
Hubert H. Humphrey Building, Suite
729D, 200 Independence Ave., SW.,
Washington, DC 20201. Please submit
one original and two copies.
• Hand Delivery or Courier: Office of
the National Coordinator for Health
Information Technology, Attention:
Revisions to ONC–AA Processes
Proposed Rule, Hubert H. Humphrey
Building, Suite 729D, 200 Independence
Ave., SW., Washington, DC 20201.
Please submit one original and two
copies. (Because access to the interior of
the Hubert H. Humphrey Building is not
readily available to persons without
Federal government identification,
commenters are encouraged to leave
their comments in the mail drop slots
located in the main lobby of the
building.)
Inspection of Public Comments: All
comments received before the close of
the comment period will be available for
public inspection, including any
personally identifiable or confidential
business information that is included in
a comment. Please do not include
anything in your comment submission
that you do not wish to share with the
general public. Such information
includes, but is not limited to: a
person’s social security number; date of
birth; driver’s license number; state
identification number or foreign country
equivalent; passport number; financial
account number; credit or debit card
number; any personal health
information; or any business
information that could be considered to
be proprietary. We will post all
comments received before the close of
the comment period at https://
www.regulations.gov.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov or the Department
of Health and Human Services, Office of
the National Coordinator for Health
Information Technology, Hubert H.
Humphrey Building, Suite 729D, 200
Independence Ave., SW., Washington,
DC 20201 (call ahead to the contact
listed below to arrange for inspection).
FOR FURTHER INFORMATION CONTACT:
Steven Posnack, Director, Federal Policy
PO 00000
Frm 00011
Fmt 4702
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Division, Office of Policy and Planning,
Office of the National Coordinator for
Health Information Technology, 202–
690–7151.
SUPPLEMENTARY INFORMATION:
Acronyms
EHR Electronic Health Record
HHS Department of Health and Human
Services
HIT Health Information Technology
HITECH Health Information Technology for
Economic and Clinical Health
ONC Office of the National Coordinator for
Health Information Technology
ONC–AA ONC-Approved Accreditor
ONC–ACB ONC-Authorized Certification
Body
ONC–ATCB ONC-Authorized Testing and
Certification Body
PHSA Public Health Service Act
RFA Regulatory Flexibility Act
SBA Small Business Administration
Table of Contents
I. Background
A. Statutory Basis for the Permanent
Certification Program
B. Regulatory Background of the
Permanent Certification Program
1. Initial Set of Standards, Implementation
Specifications, and Certification Criteria
Interim Final and Final Rules
2. Medicare and Medicaid EHR Incentive
Programs Proposed and Final Rules
3. HIT Certification Programs Proposed
Rule and the Temporary and Permanent
Certification Programs Final Rules
C. Overview of the Permanent Certification
Program
II. Provisions of the Proposed Rule
A. Removal of the ONC–AA for Improper
Conduct or Failure To Perform Its
Responsibilities
1. Conduct Violations
2. Performance Violations
3. Proposed Removal of the ONC–AA
4. Opportunity To Respond to a Proposed
Removal Notice
5. Removal of the ONC–AA
6. Extent and Duration of Removal Under
the Permanent Certification Program
B. Effects of Removing and/or Replacing
the ONC–AA
1. ONC–ACB Status
2. New ONC–AA
III. Response to Comments
IV. Collection of Information Requirements
V. Regulatory Impact Statement
I. Background
[If you choose to comment on the
background section, please include at
the beginning of your comment the
caption ‘‘Background’’ and any
additional information to clearly
identify the information about which
you are commenting.]
A. Statutory Basis for the Permanent
Certification Program
The Health Information Technology
for Economic and Clinical Health
(HITECH) Act, Title XIII of Division A
E:\FR\FM\31MYP1.SGM
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Agencies
[Federal Register Volume 76, Number 104 (Tuesday, May 31, 2011)]
[Proposed Rules]
[Pages 31271-31272]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-13404]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 141
[FRL-9313-3]
Public Meeting: Preliminary Regulatory Determinations for the
Third Contaminant Candidate List (CCL 3)
AGENCY: Environmental Protection Agency (EPA).
ACTION: Announcement of meeting.
-----------------------------------------------------------------------
SUMMARY: The 1996 Safe Drinking Water Act Amendments require the EPA to
determine every five years, whether to regulate at least five
contaminants from the current Contaminant Candidate List (CCL) with a
national primary drinking water regulation. The process of making
decisions about whether to regulate any of the unregulated contaminants
on the CCL is called Regulatory Determinations. On October 8, 2009, EPA
published the third Contaminant Candidate List (CCL 3) containing 116
unregulated contaminants. The Agency is currently in the preliminary
process of deciding whether to regulate at least five CCL 3
contaminants (i.e., Regulatory Determinations 3). The purpose of this
notice is to announce that EPA will be hosting a public stakeholder
meeting on June 16, 2011, from 1 p.m. to 5 p.m., to discuss and obtain
input on EPA's process for Regulatory Determination 3 along with the
contaminants and the technical information that the Agency is
considering. EPA expects to publish the preliminary regulatory
determinations for at least five CCL 3 contaminants in mid-2012 and
final regulatory determinations by August 2013.
DATES: The public meeting will be held in the Washington, DC
metropolitan area on Thursday, June 16, 2011, from 1 p.m. to 5 p.m.,
Eastern Daylight Savings Time. Participants will be notified of the
specific meeting room upon confirmation of registration.
FOR FURTHER INFORMATION CONTACT: For technical inquiries regarding
EPA's Regulatory Determinations for contaminants on CCL 3 contact: Mr.
Zeno Bain at (202) 564-5970 or by e-mail: bain.zeno@epa.gov. For
additional information about the drinking water Contaminant Candidate
List and the Regulatory Determinations process, please visit: https://water.epa.gov/scitech/drinkingwater/dws/ccl/index.cfm. Additional
information on these and other EPA activities under the Safe Drinking
Water Act is also available at the Safe Drinking Water Hotline at (800)
426-4791.
SUPPLEMENTARY INFORMATION: Registration: Individuals planning to attend
the Stakeholder Meeting must register for the meeting by contacting
Melissa Simic at (202) 564-7722 or by sending an e-mail to
simic.melissa@epa.gov no later than Wednesday, June 8, 2011. There is
no charge for attending the meeting but seats are limited, so register
as soon as possible. Please note that attendees will be required to
pass through security checks at the front desk and obtain a visitor's
badge. Pre-registration for this meeting will help us facilitate your
check-in.
Special Accommodations: The meeting will be held in a building
which is accessible to persons using wheel chairs or scooters. For
[[Page 31272]]
information on access or accommodations for individuals with
disabilities, please contact Melissa Simic at (202) 564-7722 or by e-
mail at simic.melissa@epa.gov. Please allow at least five business days
prior to the meeting to give EPA time to process your request.
Dated: May 24, 2011.
Eric M. Bissonette,
Acting Director, Office of Ground Water and Drinking Water.
[FR Doc. 2011-13404 Filed 5-27-11; 8:45 am]
BILLING CODE 6560-50-P