Civilian Health and Medical Program of the Uniformed Services (CHAMPUS); TRICARE Uniform Health Maintenance Organization (HMO) Benefit-Prime Enrollment Fee Exemption for Survivors of Active Duty Deceased Sponsors and Medically Retired Uniformed Services Members and Their Dependents; Withdrawal, 50359-50360 [2013-20121]
Download as PDF
Federal Register / Vol. 78, No. 160 / Monday, August 19, 2013 / Proposed Rules
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FOR FURTHER INFORMATION CONTACT:
Annette McCarthy, Center for Food
Safety and Applied Nutrition (HFS–
205), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740, 240–402–1200.
SUPPLEMENTARY INFORMATION: To
minimize the risk of serious adverse
health consequences or death from
consumption of contaminated produce,
FDA has published the proposed rule,
Standards for Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption (‘‘the produce
safety rule’’ or ‘‘the proposed rule’’) to
establish science-based minimum
standards for the safe growing,
harvesting, packing, and holding of
produce, meaning fruits and vegetables
grown for human consumption (78 FR
3504, January 16, 2013). FDA has
proposed these standards as part of our
implementation of the FDA Food Safety
Modernization Act (FSMA). These
standards would not apply to produce
that is rarely consumed raw, produce for
personal or on-farm consumption, or
produce that is not a raw agricultural
commodity. In addition, produce that
receives commercial processing that
adequately reduces the presence of
microorganisms of public health
significance would be eligible for
exemption from the requirements of this
rule. The proposed rule would set forth
procedures, processes, and practices
that minimize the risk of serious adverse
health consequences or death, including
those reasonably necessary to prevent
the introduction of known or reasonably
foreseeable biological hazards into or
onto produce and to provide reasonable
assurances that the produce is not
adulterated on account of such hazards.
We expect that the proposed rule, if
finalized as proposed, would reduce
foodborne illness associated with the
consumption of contaminated produce.
For the proposed rule, the Agency
relied on a categorical exclusion from
the need to prepare an Environmental
Assessment or EIS under 21 CFR
25.30(j). Based on currently available
information, including comments
received, and upon further analysis,
FDA has determined that the proposed
action may significantly affect the
quality of the human environment (21
CFR 25.22(b)) and, therefore, an EIS is
necessary for the final rule. For
example, switching from surface to
ground water was originally considered
a cost- and time-prohibitive option that
was unlikely to occur to any significant
extent given that monitoring data
available prior to the publication of the
proposed rule showed that Escherichia.
coli exceedance of the proposed
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standard occurred during 5 percent of
the monitoring period with 55 percent
of the incidents being no more than 2
days, as discussed in the categorical
exclusion memo (see Ref. 266 of the
proposed rule). Public comment,
subsequent to the publication of the
proposed rule, has indicated that in
some regions current irrigation practices
use water that is unlikely to meet the
proposed microbial standards for much,
if not all of the growing season.
Consequently, if such standards are
finalized, ground water is likely to be
explored as a more viable alternative
water source for irrigation in these
regions than previous information had
indicated. Given recently highlighted
concerns of ground water depletion
(Ref. 1), FDA has determined that the
use of ground water for irrigation, in
response to a microbial standard, may
significantly affect the quality of the
human environment. Similarly,
comments received caused FDA to
reevaluate the proposed requirements
for biological soil amendments of
animal origin, which propose an
increasingly stringent set of application
restrictions based on the likelihood of
the soil amendment harboring
pathogens. These proposed
requirements, if finalized, are expected
to result in changes in current use of
treated and untreated biological soil
amendments of animal origin or
potentially greater use of synthetic
fertilizers. Changes in the type or
handling of soil amendments may
significantly affect the quality of the
human environment.
The purpose of the public scoping
process for the EIS is to determine
relevant issues that will influence the
scope of the environmental analysis,
including potential alternatives, and the
extent to which those issues and
impacts will be analyzed in the EIS. The
EIS will be prepared in accordance with
section 102(2)(C) of NEPA (Pub. L. 91–
190), FDA’s NEPA implementing
regulations (21 CFR Part 25), and the
CEQ regulations for implementing
NEPA (40 CFR Parts 1500–1508).
Federal, State, and local Agencies, along
with tribes and other stakeholders that
may be interested in or affected by the
produce safety rule are invited to
participate in the scoping process. Some
Federal Agencies may request or be
requested by the FDA to participate in
the development of the environmental
analysis as a cooperating agency. FDA
has previously sought comment on
potential environmental effects as part
of the public comment period for the
proposed rule, including specific
questions regarding agricultural water,
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50359
biological soil amendments of animal
origin, and wildlife (78 FR 3504 at 3616,
3619–3620). FDA believes that these
questions are still relevant to the
environmental analysis and will
consider comments received. FDA
encourages additional comments, as
part of this scoping process, on what
specific issues, alternatives, mitigation
measures, or other information FDA
should include for further analysis in
the EIS for the produce safety rule.
References
The following reference has been
placed on display in the Division of
Dockets Management (see ADDRESSES)
and may be seen by interested persons
between 9 a.m. and 4 p.m., Monday
through Friday. (FDA has verified the
Web site address, but FDA is not
responsible for any subsequent changes
to the Web site after this document
publishes in the Federal Register.)
1. U.S. Geological Survey. 2013.
Groundwater Depletion in the United States
(1900–2008). Scientific Investigation Report
2013–5079. Available at: https://
pubs.usgs.gov/sir/2013/5079/SIR20135079.pdf. Accessed July 30, 2013.
Dated: August 13, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–20087 Filed 8–16–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD–2011–HA–0136]
RIN 0720–AB56
Civilian Health and Medical Program of
the Uniformed Services (CHAMPUS);
TRICARE Uniform Health Maintenance
Organization (HMO) Benefit—Prime
Enrollment Fee Exemption for
Survivors of Active Duty Deceased
Sponsors and Medically Retired
Uniformed Services Members and
Their Dependents; Withdrawal
Office of the Secretary, DoD.
Proposed rule; withdrawal.
AGENCY:
ACTION:
On Thursday, August 8, 2013
(78 FR 48366–48367), the Department of
Defense published a proposed rule titled
‘‘Civilian Health and Medical Program
of the Uniformed Services (CHAMPUS);
TRICARE Uniform Health Maintenance
Organization (HMO) Benefit—Prime
Enrollment Fee Exemption for Survivors
of Active Duty Deceased Sponsors and
Medically Retired Uniformed Services
SUMMARY:
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50360
Federal Register / Vol. 78, No. 160 / Monday, August 19, 2013 / Proposed Rules
Members and Their Dependents.’’
Subsequent to the publication of the
proposed rule in the Federal Register,
DoD discovered that an identical
proposed rule published in the Federal
Register on Friday, June 7, 2013 (78 FR
34292–34293). DoD is hereby
withdrawing the proposed rule that
published in the Federal Register on
Thursday, August 8, 2013.
DATES: As of August 19, 2013 the
proposed rule published August 8, 2013
(78 FR 48366–48367), is withdrawn.
FOR FURTHER INFORMATION CONTACT:
Patricia Toppings, 571–372–0485.
Dated: August 14, 2013.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2013–20121 Filed 8–16–13; 8:45 am]
BILLING CODE 5001–06–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R05–OAR–2011–0888; EPA–R05–
OAR–2011–0969; EPA–R05–OAR–2012–
0567; EPA–R05–OAR–2012–0988; FRL–
9900–19–Region 5]
Approval and Promulgation of Air
Quality Implementation Plans; Indiana;
Infrastructure SIP Requirements for
the 2008 Lead and Ozone National
Ambient Air Quality Standards; Indiana
PSD; Indiana State Board
Requirements
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
EPA is proposing to approve
elements of state implementation plan
(SIP) submissions by Indiana regarding
the infrastructure requirements of
sections 110(a)(1) and (2) of the Clean
Air Act (CAA) for the 2008 lead and
2008 8-hour ground level ozone national
ambient air quality standards (2008 Pb
and ozone NAAQS). The infrastructure
requirements are designed to ensure that
the structural components of each
state’s air quality management program
are adequate to meet the state’s
responsibilities under the CAA. EPA is
also proposing to approve portions of
submissions from Indiana addressing
EPA’s requirements for the prevention
of significant deterioration (PSD)
program. Lastly, EPA is proposing to
approve a submission from Indiana
addressing the state board requirements
under section 128 of the CAA.
DATES: Comments must be received on
or before September 18, 2013.
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SUMMARY:
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Submit your comments,
identified by Docket ID No. EPA–R05–
OAR–2011–0888 (2008 Pb infrastructure
SIP elements), EPA–R05–OAR–2011–
0969 (2008 ozone infrastructure SIP
elements), EPA–R05–OAR–2012–0567
(PSD elements), or EPA–R05–OAR–
2012–0988 (state board requirements),
by one of the following methods:
1. www.regulations.gov: Follow the
on-line instructions for submitting
comments.
2. Email: aburano.douglas@epa.gov.
3. Fax: (312) 408–2279.
4. Mail: Douglas Aburano, Chief,
Attainment Planning and Maintenance
Section, Air Programs Branch (AR–18J),
U.S. Environmental Protection Agency,
77 West Jackson Boulevard, Chicago,
Illinois 60604.
5. Hand Delivery: Douglas Aburano,
Chief, Attainment Planning and
Maintenance Section, Air Programs
Branch (AR–18J), U.S. Environmental
Protection Agency, 77 West Jackson
Boulevard, Chicago, Illinois 60604.
Such deliveries are only accepted
during the Regional Office normal hours
of operation, and special arrangements
should be made for deliveries of boxed
information. The Regional Office official
hours of business are Monday through
Friday, 8:30 a.m. to 4:30 p.m., excluding
Federal holidays.
Instructions: Direct your comments to
Docket ID. EPA–R05–OAR–2011–0888
(2008 Pb infrastructure SIP elements),
EPA–R05–OAR–2011–0969 (2008 ozone
infrastructure SIP elements), EPA–R05–
OAR–2012–0567 (PSD elements), or
EPA–R05–OAR–2012–0988 (state board
requirements). EPA’s policy is that all
comments received will be included in
the public docket without change and
may be made available online at
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through www.regulations.gov
or email. The www.regulations.gov Web
site is an ‘‘anonymous access’’ system,
which means EPA will not know your
identity or contact information unless
you provide it in the body of your
comment. If you send an email
comment directly to EPA without going
through www.regulations.gov your email
address will be automatically captured
and included as part of the comment
that is placed in the public docket and
made available on the Internet. If you
submit an electronic comment, EPA
recommends that you include your
name and other contact information in
ADDRESSES:
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the body of your comment and with any
disk or CD–ROM you submit. If EPA
cannot read your comment due to
technical difficulties and cannot contact
you for clarification, EPA may not be
able to consider your comment.
Electronic files should avoid the use of
special characters, any form of
encryption, and be free of any defects or
viruses.
Docket: All documents in the docket
are listed in the www.regulations.gov
index. Although listed in the index,
some information is not publicly
available, e.g., CBI or other information
whose disclosure is restricted by statute.
Certain other material, such as
copyrighted material, will be publicly
available only in hard copy. Publicly
available docket materials are available
either electronically in
www.regulations.gov or in hard copy at
the U.S. Environmental Protection
Agency, Region 5, Air and Radiation
Division, 77 West Jackson Boulevard,
Chicago, Illinois 60604. This facility is
open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding
Federal holidays. We recommend that
you telephone Andy Chang,
Environmental Engineer, at (312) 886–
0258 before visiting the Region 5 office.
FOR FURTHER INFORMATION CONTACT:
Andy Chang, Environmental Engineer,
Attainment Planning and Maintenance
Section, Air Programs Branch (AR–18J),
U.S. Environmental Protection Agency,
Region 5, 77 West Jackson Boulevard,
Chicago, Illinois 60604, (312) 886–0258,
chang.andy@epa.gov.
SUPPLEMENTARY INFORMATION:
Throughout this document whenever
‘‘we,’’ ‘‘us,’’ or ‘‘our’’ is used, we mean
EPA. This supplementary information
section is arranged as follows:
I. What should I consider as I prepare my
comments for EPA?
II. What is the background of these SIP
submissions?
A. What state SIP submissions does this
rulemaking address?
B. Why did the state make these SIP
submissions?
C. What is the scope of this rulemaking?
III. What guidance is EPA using to evaluate
these SIP submissions?
IV. What is the result of EPA’s review of
these SIP submissions?
A. Section 110(a)(2)(A)—Emission Limits
and Other Control Measures
B. Section 110(a)(2)(B)—Ambient Air
Quality Monitoring/Data System
C. Section 110(a)(2)(C)—Program for
Enforcement of Control Measures; PSD
D. Section 110(a)(2)(D)—Interstate
Transport
E. Section 110(a)(2)(E)—Adequate
Resources
F. Section 110(a)(2)(F)—Stationary Source
Monitoring System
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Agencies
[Federal Register Volume 78, Number 160 (Monday, August 19, 2013)]
[Proposed Rules]
[Pages 50359-50360]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-20121]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD-2011-HA-0136]
RIN 0720-AB56
Civilian Health and Medical Program of the Uniformed Services
(CHAMPUS); TRICARE Uniform Health Maintenance Organization (HMO)
Benefit--Prime Enrollment Fee Exemption for Survivors of Active Duty
Deceased Sponsors and Medically Retired Uniformed Services Members and
Their Dependents; Withdrawal
AGENCY: Office of the Secretary, DoD.
ACTION: Proposed rule; withdrawal.
-----------------------------------------------------------------------
SUMMARY: On Thursday, August 8, 2013 (78 FR 48366-48367), the
Department of Defense published a proposed rule titled ``Civilian
Health and Medical Program of the Uniformed Services (CHAMPUS); TRICARE
Uniform Health Maintenance Organization (HMO) Benefit--Prime Enrollment
Fee Exemption for Survivors of Active Duty Deceased Sponsors and
Medically Retired Uniformed Services
[[Page 50360]]
Members and Their Dependents.'' Subsequent to the publication of the
proposed rule in the Federal Register, DoD discovered that an identical
proposed rule published in the Federal Register on Friday, June 7, 2013
(78 FR 34292-34293). DoD is hereby withdrawing the proposed rule that
published in the Federal Register on Thursday, August 8, 2013.
DATES: As of August 19, 2013 the proposed rule published August 8, 2013
(78 FR 48366-48367), is withdrawn.
FOR FURTHER INFORMATION CONTACT: Patricia Toppings, 571-372-0485.
Dated: August 14, 2013.
Aaron Siegel,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 2013-20121 Filed 8-16-13; 8:45 am]
BILLING CODE 5001-06-P