Agency Information Collection Activities; Proposed Collection; Comment Request; Semi-Annual and Final Reporting Requirements for Discretionary Grant Programs, 47396-47397 [2012-19453]
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47396
Federal Register / Vol. 77, No. 153 / Wednesday, August 8, 2012 / Notices
ANNUAL BURDEN ESTIMATES
Number of respondents
Instrument
ORR–3 .........................................................
ORR–4 .........................................................
Estimated Total Annual Burden
Hours: 2512.5.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded 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.
Email address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012–19418 Filed 8–7–12; 8:45 am]
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Estimate responses 75 ................................
Estimate responses 119 ..............................
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Semi-Annual and
Final Reporting Requirements for
Discretionary Grant Programs
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
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 the continuation of an
existing collection for Performance
Progress Reports previously approved
for discretionary grants funded by the
U.S. Administration on Aging (AoA),
which is now a part of ACL.
DATES: Submit written or electronic
comments on the collection of
information by October 9, 2012.
ADDRESSES: Submit electronic
comments on the collection of
information to:
lori.stalbaum@aoa.hhs.gov. Submit
written comments on the collection of
information to Lori Stalbaum,
Administration on Aging, Washington,
DC 20201 or by fax to Lori Stalbaum at
202–357–3469. .
FOR FURTHER INFORMATION CONTACT: Lori
Stalbaum at 202–357–3452 or
lori.stalbaum@aoa.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
SUMMARY:
PO 00000
Frm 00039
Average burden hours per
response
Number of responses per respondent
Fmt 4703
Sfmt 4703
0.25
1.25
Total burden
hours
Estimated 281.25
Estimated
2231.25
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 Administration for Community
Living (ACL) plans to continue an
existing approved collection of
information for semi-annual and final
reports pursuant to the requirements of
its discretionary grant programs.
Through its discretionary grant
programs, ACL supports projects for the
purpose of developing and testing new
knowledge and program innovations
with the potential for contributing to the
independence, well-being, and health of
older adults, people with disabilities
across the lifespan, and their families
and caregivers. Deliverables required by
ACL of all Title IV grantees are semiannual and final reports, as provided for
in the Department of Health and Human
Services regulations, 45CFR Part 74,
Section 74.51. These Title IV grantee
performance reporting requirements can
be found on ACL’s Web site at https://
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Federal Register / Vol. 77, No. 153 / Wednesday, August 8, 2012 / Notices
www.aoa.gov/AoARoot/Grants/
Reporting_Requirements/docs/
FinalReportHandbook.doc. ACL
estimates the burden of this collection
of information as follows: Frequency:
Semi-annually with the Final report
taking the place of the semi-annual
report at the end of the final year of the
grant. Respondents: States, public
agencies, private nonprofit agencies,
institutions of higher education, and
organizations including tribal
organizations. Estimated Number of
Responses: 600. Total Estimated Burden
Hours: 12,000.
Dated: August 3, 2012.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
information collection and has assigned
OMB control number 0910–0291. The
approval expires on June 30, 2015. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
Dated: August 3, 2012.
David Dorsey,
Acting Associate Commissioner for Policy and
Planning.
[FR Doc. 2012–19377 Filed 8–7–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FR Doc. 2012–19453 Filed 8–7–12; 8:45 am]
[Docket No. FDA–2012–N–0793]
BILLING CODE 4154–01–P
Request for Nominations of Specific
Drug/Biologic Product(s) That Could
Be Brought Before the Food and Drug
Administration’s Pediatric
Subcommittee of the Oncologic Drugs
Advisory Committee
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0608]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
MedWatch: The Food and Drug
Administration Medical Products
Reporting Program
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘MedWatch: The Food and Drug
Administration Medical Products
Reporting Program’’ has been approved
by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3794,
Jonnalynn.Capezzuto@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On June
28, 2012, the Agency submitted a
proposed collection of information
entitled ‘‘MedWatch: The Food and
Drug Administration Medical Products
Reporting Program’’ to OMB for review
and clearance under 44 U.S.C. 3507. An
Agency may not conduct or sponsor,
and a person is not required to respond
to, a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
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SUMMARY:
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AGENCY:
Food and Drug Administration,
HHS.
Notice; request for product
nominations.
ACTION:
The Food and Drug
Administration’s (FDA) Office of
Hematology and Oncology Products
invites the public to suggest one or more
specific drug or biologic products that
could be brought before the December 4,
2012, Pediatric Subcommittee of the
Oncologic Drugs Advisory Committee
(ODAC). The number of drugs studied
for use in pediatric patients is growing,
and we see a reduction in off-label use.
However, we would like to improve
current and future pediatric product
development by focusing on products
whose development would benefit the
most from the attention of an advisory
committee. The company developing a
product that is brought before the
committee will be given the unique
opportunity to present proposed
pediatric studies in the United States,
share their plans for global pediatric
development, and hear discussions by
the Pediatric Subcommittee on possible
directions for their current or future
pediatric oncology product
development.
SUMMARY:
Nominations must be received
by September 4, 2012, to receive
consideration for inclusion.
Nominations received after this date
will receive consideration for future
meetings of the Pediatric Subcommittee
of the ODAC.
DATES:
PO 00000
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Fmt 4703
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47397
Email nominations to
Christine.Lincoln@fda.hhs.gov, and
please include the subject line
‘‘Suggested Product for 2012 Pediatric
Oncology Subcommittee of ODAC.’’
FOR FURTHER INFORMATION CONTACT:
Christine Lincoln, RN, MS, MBA, Center
for Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, Rm. 2206,
Silver Spring, MD 20993, 301–796–
4117, Christine.Lincoln@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: The Food
and Drug Administration (FDA)
Advisory Committees are an important,
transparent interface that allows the
Agency to include the public in its
decision-making processes. Significant
public health and safety issues are
brought before these committees for
deliberation, and the meetings bring
together both experts with state-of-theart knowledge and members of the
public with relevant personal
experiences. This broad participation
gives FDA a unique perspective as it
seeks to assure the safety, efficacy, and
security of FDA-regulated products.
Additional information about the
prior November 2, 2011, Pediatric
Oncology Subcommittee of the
Oncologic Drugs Advisory Committee
may be found on FDA’s Web site at:
https://www.fda.gov/
AdvisoryCommittees/Calendar/
ucm274396.htm.
ADDRESSES:
Dated: August 2, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012–19330 Filed 8–7–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Statement of Organization, Functions
and Delegations of Authority
This notice amends Part R of the
Statement of Organization, Functions
and Delegations of Authority of the
Department of Health and Human
Services (HHS), Health Resources and
Services Administration (HRSA) (60 FR
56605, as amended November 6, 1995;
as last amended at 77 FR 46098–46099
dated August 2, 2012).
This notice reflects organizational
changes in the Health Resources and
Services Administration (HRSA).
Specifically, this notice updates the
functional statement for both the Office
of Operations (RB) and the Office of
Management (RB4) to include the
human resources function for HRSA;
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]]>Agencies
[Federal Register Volume 77, Number 153 (Wednesday, August 8, 2012)]
[Notices]
[Pages 47396-47397]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-19453]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; Semi-Annual and Final Reporting Requirements for
Discretionary Grant Programs
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 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 the continuation of an existing collection for
Performance Progress Reports previously approved for discretionary
grants funded by the U.S. Administration on Aging (AoA), which is now a
part of ACL.
DATES: Submit written or electronic comments on the collection of
information by October 9, 2012.
ADDRESSES: Submit electronic comments on the collection of information
to: lori.stalbaum@aoa.hhs.gov. Submit written comments on the
collection of information to Lori Stalbaum, Administration on Aging,
Washington, DC 20201 or by fax to Lori Stalbaum at 202-357-3469. .
FOR FURTHER INFORMATION CONTACT: Lori Stalbaum at 202-357-3452 or
lori.stalbaum@aoa.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 Administration for Community Living (ACL) plans to continue an
existing approved collection of information for semi-annual and final
reports pursuant to the requirements of its discretionary grant
programs. Through its discretionary grant programs, ACL supports
projects for the purpose of developing and testing new knowledge and
program innovations with the potential for contributing to the
independence, well-being, and health of older adults, people with
disabilities across the lifespan, and their families and caregivers.
Deliverables required by ACL of all Title IV grantees are semi-annual
and final reports, as provided for in the Department of Health and
Human Services regulations, 45CFR Part 74, Section 74.51. These Title
IV grantee performance reporting requirements can be found on ACL's Web
site at https://
[[Page 47397]]
www.aoa.gov/AoARoot/Grants/Reporting_Requirements/docs/
FinalReportHandbook.doc. ACL estimates the burden of this collection of
information as follows: Frequency: Semi-annually with the Final report
taking the place of the semi-annual report at the end of the final year
of the grant. Respondents: States, public agencies, private nonprofit
agencies, institutions of higher education, and organizations including
tribal organizations. Estimated Number of Responses: 600. Total
Estimated Burden Hours: 12,000.
Dated: August 3, 2012.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2012-19453 Filed 8-7-12; 8:45 am]
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