Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB); Extension of Comment Period, 4413-4414 [2013-01172]
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Federal Register / Vol. 78, No. 14 / Tuesday, January 22, 2013 / Notices
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 currently
approved collection. Title of
Information Collection: Medicare Parts
C and D Universal Audit Guide. Use:
Under the Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 and implementing regulations
under 42 CFR parts 422 and 423,
Medicare Part D plan sponsors and
Medicare Advantage organizations are
required to comply with all Medicare
Parts C and D program requirements. In
2010 the explosive growth of these
sponsoring organizations forced CMS to
develop an audit strategy to ensure we
continue to obtain meaningful audit
results. As a result, CMS’ audit strategy
reflected a move to a more targeted,
data-driven and risk-based audit
approach that focused on high-risk areas
having the greatest potential for
beneficiary harm.
To accomplish this we have combined
all Part C and Part D audit elements into
one universal guide which will also
promote consistency, effectiveness and
reduce financial and time burdens for
both CMS and Medicare-contracting
entities. The combined Medicare Part C
& D Universal Audit Guide received
OMB approval in 2010. The Health Plan
Management System (HPMS) is the
current conduit by which organizations
submit many sources of audit materials
such as bids and other ongoing updates
to CMS. Please note the guide is very
comprehensive in that it describes all
areas that could be audited. Due to
limited resources, CMS is unable to
audit all areas for any particular
sponsor. Some areas could be monitored
by the account manager, etc. Other areas
could be audited in the program audits.
To maximize resources, CMS will
focus on assisting the industry to
improve their operations to ensure
beneficiaries receive access to care. One
way to accomplish this is CMS will
develop an annual audit strategy which
describes how sponsors will be selected
for audit and the areas that will be
audited. The audit strategy will be
shared with the industry via the CMS
Web site, HPMS memo, the Part C & D
user call, and other conferences. Once
the audit areas are defined, CMS will
design audit protocols describing in
detail the focus of the audit, the data
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required for the audit, etc. The
Engagement Letter and Protocols will be
sent to all sponsors selected for audit 4
weeks prior to starting the audit. In
addition, the protocols will be released
to the industry at the beginning of each
calendar year via the same manner as
the audit strategy. To assist in
improving the audit process, CMS sends
the plan sponsors a survey at the end of
each audit to complete in order to
obtain the sponsor’s feedback. The
sponsor is not required to complete the
survey.
Form Number: CMS–10191 (OCN
0938–1000). Frequency: Yearly. Affected
Public: Private Sector (business or other
for-profit and not-for-profit institutions).
Number of Respondents: 195. Total
Annual Responses: 195. Total Annual
Hours: 24,180. (For policy questions
regarding this collection contact Tracey
Roberts at 410–786–8643. 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 March 25, 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: January 16, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
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4413
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10453]
Public Information Collection
Requirements Submitted to the Office
of Management and Budget (OMB);
Extension of Comment Period
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Agency information collection
activities: Proposed collection; comment
request; extension of comment period.
AGENCY:
This notice extends the
comment period for a 60-day notice
request for proposed information
collection request associated with the
notice [Document Identifier: CMS–
10453] entitled ‘‘The Medicare
Advantage and Prescription Drug
Program: Part C Explanation of Benefits
CFR 422.111(b)(12)’’ that was published
in the November 26, 2012 (77 FR 70445)
Federal Register. The comment period
for the information collection request,
which would have ended on January 25,
2013, is extended to February 1, 2013.
DATES: The comment period for the
information collection request
published in the January 25, 2013,
Federal Register (77 FR 70445) is
extended to February 1, 2013.
FOR FURTHER INFORMATION CONTACT:
William Parham, (410) 786–4669.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
In the FR Doc. 2012–28570 of
November 26, 2012 (77 FR 70445), we
published a Paperwork Reduction Act
notice requesting a 60-day public
comment period for the document
entitled ‘‘The Medicare Advantage and
Prescription Drug Program: Part C
Explanation of Benefits CFR
422.111(b)(12).’’
There were technical delays with
making the information collection
request publicly available; therefore, in
this notice we are extending the
comment period from the date originally
listed in the November 26, 2012, notice.
II. Extension of Comment Period
We are extending the comment period
for the notice [Document Identifier:
CMS–10453] in FR Doc. 2012–28570
published on November 26, 2012 (77 FR
70445).
The date listed on page 70445, third
column, second full paragraph, on the
fifth line in the paragraph beginning
with ‘‘To be assured consideration,
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Federal Register / Vol. 78, No. 14 / Tuesday, January 22, 2013 / Notices
comments and recommendations must
be submitted in one of the following
ways by January 25, 2013.’’ has been
extended to February 1, 2013.’’
Dated: January 16, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Procedures for Requests from
Tribal Lead Agencies to use Child Care
and Development Fund (CCDF) Funds
for Construction or Major Renovation of
Child Care Facilities.
OMB No.: 0970–0160.
Description: The Child Care and
Development Block Grant Act, as
amended, allows Indian Tribes to use
Child Care and Development Fund
(CCDF) grant awards for construction
and renovation of child care facilities. A
tribal grantee must first request and
receive approval from the
[FR Doc. 2013–01172 Filed 1–18–13; 8:45 am]
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Administration for Children and
Families (ACF) before using CCDF funds
for construction or major renovation.
This information collection contains the
statutorily-mandated uniform
procedures for the solicitation and
consideration of requests, including
instructions for preparation of
environmental assessments in
conjunction with the National
Environmental Policy Act. The
proposed draft procedures update the
procedures that were originally issued
in August 1997 and last updated in
April 2010. Respondents will be CCDF
tribal grantees requesting to use CCDF
funds for construction or major
renovation.
Respondents: Tribal Child Care Lead
Agencies acting on behalf of Tribal
Governments.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Construction or Major Renovation of Tribal Child Care Facilities ...................
5
1
20
100
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Estimated Total Annual Burden
Hours: 100.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
L’Enfant Promenade SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
Email:
OIRA_SUBMISSION@OMB.EOP.GOV,
Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013–01117 Filed 1–18–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0065]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Registration of
Food Facilities Under the Public Health
Security and Bioterrorism
Preparedness and Response Act of
2002
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
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 provisions of
the Agency’s regulations that require
registration for domestic and foreign
facilities that manufacture, process,
SUMMARY:
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pack, or hold food for human or animal
consumption in the United States.
DATES: Submit either electronic or
written comments on the collection of
information by March 25, 2013.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Domini Bean, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400T, Rockville, MD 20850,
domini.bean@fda.hhs.gov.
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 requests
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
SUPPLEMENTARY INFORMATION:
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Agencies
[Federal Register Volume 78, Number 14 (Tuesday, January 22, 2013)]
[Notices]
[Pages 4413-4414]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-01172]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10453]
Public Information Collection Requirements Submitted to the
Office of Management and Budget (OMB); Extension of Comment Period
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Agency information collection activities: Proposed collection;
comment request; extension of comment period.
-----------------------------------------------------------------------
SUMMARY: This notice extends the comment period for a 60-day notice
request for proposed information collection request associated with the
notice [Document Identifier: CMS-10453] entitled ``The Medicare
Advantage and Prescription Drug Program: Part C Explanation of Benefits
CFR 422.111(b)(12)'' that was published in the November 26, 2012 (77 FR
70445) Federal Register. The comment period for the information
collection request, which would have ended on January 25, 2013, is
extended to February 1, 2013.
DATES: The comment period for the information collection request
published in the January 25, 2013, Federal Register (77 FR 70445) is
extended to February 1, 2013.
FOR FURTHER INFORMATION CONTACT: William Parham, (410) 786-4669.
SUPPLEMENTARY INFORMATION:
I. Background
In the FR Doc. 2012-28570 of November 26, 2012 (77 FR 70445), we
published a Paperwork Reduction Act notice requesting a 60-day public
comment period for the document entitled ``The Medicare Advantage and
Prescription Drug Program: Part C Explanation of Benefits CFR
422.111(b)(12).''
There were technical delays with making the information collection
request publicly available; therefore, in this notice we are extending
the comment period from the date originally listed in the November 26,
2012, notice.
II. Extension of Comment Period
We are extending the comment period for the notice [Document
Identifier: CMS-10453] in FR Doc. 2012-28570 published on November 26,
2012 (77 FR 70445).
The date listed on page 70445, third column, second full paragraph,
on the fifth line in the paragraph beginning with ``To be assured
consideration,
[[Page 4414]]
comments and recommendations must be submitted in one of the following
ways by January 25, 2013.'' has been extended to February 1, 2013.''
Dated: January 16, 2013.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2013-01172 Filed 1-18-13; 8:45 am]
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