Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; MedWatch: The Food and Drug Administration Medical Products Reporting Program, 47397 [2012-19377]
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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]
BILLING CODE 4160–01–P
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
wreier-aviles on DSK7SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
15:11 Aug 07, 2012
Jkt 226001
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
Frm 00040
Fmt 4703
Sfmt 4703
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]
BILLING CODE 4160–01–P
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;
E:\FR\FM\08AUN1.SGM
08AUN1
Agencies
[Federal Register Volume 77, Number 153 (Wednesday, August 8, 2012)]
[Notices]
[Page 47397]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-19377]
-----------------------------------------------------------------------
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.
-----------------------------------------------------------------------
SUMMARY: 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 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]
BILLING CODE 4160-01-P