Agency Information Collection Activities; Proposed Collection; Comment Request; State Program Report, 9927-9928 [2013-03139]
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Federal Register / Vol. 78, No. 29 / Tuesday, February 12, 2013 / Notices
forth in Section 552b(c) (4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters To Be Discussed: The meeting will
include the initial review, discussion, and
evaluation of applications received in
response to ‘‘Cost-Benefit of Incentive-based
Smoking Cessation for Pregnant Women,
FOA DP 13–003, initial review.’’
Contact Person for More Information: M.
Chris Langub, Ph.D., Scientific Review
Officer, CDC, 4770 Buford Highway, NE.,
Mailstop F–46, Atlanta, Georgia 30341,
Telephone: (770) 488–3585, EEO6@cdc.gov.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2013–03130 Filed 2–11–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–685 and CMS–
R–290]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: Revision of a previously
approved collection; Title of
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AGENCY:
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Information Collection: End Stage Renal
Disease (ESRD) Network Semi-Annual
Cost Report Forms and Supporting
Regulations in 42 CFR section 405.2110
and 42 CFR 405.2112; Use: Section
1881(c) of the Social Security Act
establishes End Stage Renal Disease
(ESRD) Network contracts. The
regulations found at 42 CFR 405.2110
and 405.2112 designated 18 ESRD
Networks which are funded by
renewable contracts. These contracts are
on 3-year cycles. To better administer
the program, CMS is requiring
contractors to submit semi-annual cost
reports. The purpose of the cost reports
is to enable the ESRD Networks to
report costs in a standardized manner.
This will allow CMS to review, compare
and project ESRD Network costs during
the life of the contract. Since the last
collection, the survey instrument has
been revised. The burden has not
changed. Form Number: CMS–685
(OMB#: 0938–0657); Frequency:
Reporting—Semi-annually; Affected
Public: Not-for-profit institutions;
Number of Respondents: 18; Total
Annual Responses: 36; Total Annual
Hours: 108. (For policy questions
regarding this collection contact
Benjamin Bernstein at 410–786–6570.
For all other issues call 410–786–1326.)
2. Type of Information Collection
Request: Reinstatement of a currently
approved collection; Title: Medicare
Program: Procedures for Making
National Coverage Decisions; Use: The
Centers for Medicare & Medicaid
Services (CMS) revised the April 27,
1999 (64 FR 22619) notice and
published a new notice on September
26, 2003 (68 FR 55634) that described
the process we use to make Medicare
coverage decisions including decisions
regarding whether new technology and
services can be covered. We have made
changes to our internal procedures in
response to the comments we received
following publication of the 1999 notice
and experience under our new process.
Over the past several years, we received
numerous suggestions to further revise
our process to continue to make it more
open, responsive, and understandable to
the public. We share the goal of
increasing public participation in the
development of Medicare coverage
issues. This will assist us in obtaining
the information we require to make a
national coverage determination in a
timely manner and ensuring that the
Medicare program continues to meet the
needs of its beneficiaries. Form Number:
CMS–R–290 (OCN: 0938–0776);
Frequency: Annual; Affected Public:
Private Sector: Business or other forprofits; Number of Respondents: 200;
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9927
Total Annual Responses: 200; Total
Annual Hours: 8,000. (For policy
questions regarding this collection
contact Katherine Tillman at 410–786–
9252. For all other issues call 410–786–
1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or
Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by April 15, 2013:
1. Electronically. You may submit
your comments electronically to
https://www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
2. By Regular Mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number __, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: February 6, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2013–03059 Filed 2–11–13; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; State Program
Report
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
an opportunity for public comment on
the proposed collection of certain
information by the agency. Under the
SUMMARY:
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9928
Federal Register / Vol. 78, No. 29 / Tuesday, February 12, 2013 / Notices
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the information collection requirements
relating to Title III and VII State
Program Report.
DATES: Submit written or electronic
comments on the collection of
information by April 15, 2013.
ADDRESSES: Submit electronic
comments on the collection of
information to: Elena.Fazio@acl.hhs.gov
Submit written comments on the
collection of information to: U.S.
Department of Health and Human
Services: Administration for
Community Living, Washington, DC
20201, Attention: Elena Fazio.
FOR FURTHER INFORMATION CONTACT:
Elena Fazio by telephone: (202)357–
3583 or by email:
Elena.Fazio@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency request
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, ACL is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following collection
of information, ACL invites comments
on: (1) Whether the proposed collection
of information is necessary for the
proper performance of ACL’s functions,
including whether the information will
have practical utility; (2) the accuracy of
ACL’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) ways to minimize the
burden of the collection of information
on respondents, including through the
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16:40 Feb 11, 2013
Jkt 229001
use of automated collection techniques
when appropriate, and other forms of
information technology.
The Older Americans Act (OAA)
requires annual program performance
reports from States. In compliance with
this OAA provision, ACL developed a
State Program Report (SPR) in 1996 as
part of its National Aging Program
Information System (NAPIS). The SPR
collects information about how State
Agencies on Aging expend their OAA
funds as well as funding from other
sources for OAA authorized supportive
services. The SPR also collects
information on the demographic and
functional status of the recipients, and
is a key source for ACL performance
measurement. This collection includes
minor revisions of the format from the
2010 approved version. The proposed
revised version will be in effect for the
FY 2014 reporting year and thereafter,
while the current reporting, OMB
Approval Number 0985–0008, will be
extended to the end of the FY 2013
reporting cycle. The proposed FY 2014
version may be found on the ACL Web
site link entitled Proposed SPR for
Review available at https://www.aoa.gov/
AoARoot/Program_Results/
OAA_Performance.aspx#national.
ACL estimates the burden of this
collection of information as follows:
2,828 hours.
Dated: February 6, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2013–03139 Filed 2–11–13; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0124]
Food and Drug Administration Drug
Shortages Task Force and Strategic
Plan; Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; request for comments.
To assist the Food and Drug
Administration (FDA or Agency) in
drafting a strategic plan on drug
shortages as required by the Food and
Drug Administration Safety and
Innovation Act, the Agency is seeking
public comment from interested persons
on certain questions related to drug and
biological product shortages.
DATES: Submit either electronic or
written comments by March 14, 2013.
SUMMARY:
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You may submit comments,
identified by Docket No. FDA–2013–N–
0124, by any of the following methods:
Electronic Submissions:
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Written Submissions:
Submit written submissions in the
following way:
• Mail/Hand delivery/Courier (for
paper or CD–ROM submissions):
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
Instructions: All submissions received
must include the Agency name and
Docket No. FDA–2013–N–0124. All
comments received may be posted
without change to https://
www.regulations.gov, including any
personal information provided. For
additional information on submitting
comments, see the ‘‘Comments’’ heading
of the SUPPLEMENTARY INFORMATION
section of this document.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Kalah Auchincloss, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 6208;
Silver Spring, MD 20993, 301–796–
0659.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. Background
On July 9, 2012, the President signed
into law the Food and Drug
Administration Safety and Innovation
Act (FDASIA) (Pub. L. 112–144).
Section 1003 of FDASIA adds section
506D to the Federal Food, Drug, and
Cosmetic Act (the FD&C Act) to require
the formation of a task force to develop
and implement a strategic plan for
enhancing the Agency’s response to
preventing and mitigating drug
shortages. Section 506D of the FD&C Act
(21 U.S.C. 356D) requires that the drug
shortages strategic plan include the
following:
• Plans for enhanced interagency and
intra-agency coordination,
communication, and decisionmaking;
• Plans for ensuring that drug
shortages are considered when the
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Agencies
[Federal Register Volume 78, Number 29 (Tuesday, February 12, 2013)]
[Notices]
[Pages 9927-9928]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-03139]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; State Program Report
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing an
opportunity for public comment on the proposed collection of certain
information by the agency. Under the
[[Page 9928]]
Paperwork Reduction Act of 1995 (the PRA), Federal agencies are
required to publish notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
of an existing collection of information, and to allow 60 days for
public comment in response to the notice. This notice solicits comments
on the information collection requirements relating to Title III and
VII State Program Report.
DATES: Submit written or electronic comments on the collection of
information by April 15, 2013.
ADDRESSES: Submit electronic comments on the collection of information
to: Elena.Fazio@acl.hhs.gov Submit written comments on the collection
of information to: U.S. Department of Health and Human Services:
Administration for Community Living, Washington, DC 20201, Attention:
Elena Fazio.
FOR FURTHER INFORMATION CONTACT: Elena Fazio by telephone: (202)357-
3583 or by email: Elena.Fazio@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency request or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A))
requires Federal agencies to provide a 60-day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information,
before submitting the collection to OMB for approval. To comply with
this requirement, ACL is publishing notice of the proposed collection
of information set forth in this document. With respect to the
following collection of information, ACL invites comments on: (1)
Whether the proposed collection of information is necessary for the
proper performance of ACL's functions, including whether the
information will have practical utility; (2) the accuracy of ACL's
estimate of the burden of the proposed collection of information,
including the validity of the methodology and assumptions used; (3)
ways to enhance the quality, utility, and clarity of the information to
be collected; and (4) ways to minimize the burden of the collection of
information on respondents, including through the use of automated
collection techniques when appropriate, and other forms of information
technology.
The Older Americans Act (OAA) requires annual program performance
reports from States. In compliance with this OAA provision, ACL
developed a State Program Report (SPR) in 1996 as part of its National
Aging Program Information System (NAPIS). The SPR collects information
about how State Agencies on Aging expend their OAA funds as well as
funding from other sources for OAA authorized supportive services. The
SPR also collects information on the demographic and functional status
of the recipients, and is a key source for ACL performance measurement.
This collection includes minor revisions of the format from the 2010
approved version. The proposed revised version will be in effect for
the FY 2014 reporting year and thereafter, while the current reporting,
OMB Approval Number 0985-0008, will be extended to the end of the FY
2013 reporting cycle. The proposed FY 2014 version may be found on the
ACL Web site link entitled Proposed SPR for Review available at https://www.aoa.gov/AoARoot/Program_Results/OAA_Performance.aspx#national.
ACL estimates the burden of this collection of information as
follows: 2,828 hours.
Dated: February 6, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2013-03139 Filed 2-11-13; 8:45 am]
BILLING CODE 4154-01-P