Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; General Administrative Procedures: Citizen Petitions; Petition for Reconsideration or Stay of Action; Advisory Opinions, 27502 [E6-7157]
Download as PDF
27502
Federal Register / Vol. 71, No. 91 / Thursday, May 11, 2006 / Notices
cchase on PROD1PC60 with NOTICES
announces the following subcommittee
and committee meetings.
Name: Science and Program Review
Subcommittee (SPRS).
Times and Dates: 6:30 p.m.–9:30 p.m., June
12, 2006. 8 a.m.–11:30 a.m., June 13, 2006.
Place: Doubletree Hotel Atlanta, 3342
Peachtree Road, NE., Atlanta, GA 30326.
Status: Open: 6:30 p.m.–7 p.m., June 12,
2006. Closed: 7 p.m.–9:30 p.m., June 12,
2006. Closed: 8 a.m.–10 a.m., June 13, 2006.
Open: 10 a.m.–11:30 a.m., June 13, 2006.
Purpose: The SPRS provides advice on the
needs, structure, progress and performance of
programs of the National Center for Injury
Prevention and Control (NCIPC), as well as
second-level scientific and programmatic
review for applications for research grants,
cooperative agreements, and training grants
related to injury control and violence
prevention, and recommends approval of
projects that merit further consideration for
funding support. The SPRS also advises on
priorities for research to be supported by
contracts, grants, and cooperative agreements
and provides concept review of program
proposals and announcements.
Matters to be Discussed: The subcommittee
will meet June 12–13 to provide a secondary
review, discuss, and evaluate grant
applications and cooperative agreements
received in response to eight Request for
Applications (RFAs) related to the following
individual applications: #06001, Research
Grants to Prevent Unintentional Injuries;
#06002, Dissertation Grant Awards for
Violence Injury Research in Minority
Communities; #06003, Research Grants to
Describe Traumatic Brain Injury
Consequences; #06004, Grants for ViolenceRelated Injury Prevention Research; #06005,
Research Grants for the Care of the Acutely
Injured; #06006, Using Technology to
Augment Effectiveness of Parenting
Programs; #06007, Evaluation of CommunityBased Approaches to Increasing Seat Belt Use
among Adolescents and Their Passengers;
#06008, Urban Partnership Academic Centers
of Excellence. This portion of the meeting (7
p.m.–9:30 p.m., June 12, 2006, and 8 a.m.–
10 a.m., June 13, 2006) will be closed to the
public in accordance with provisions set
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.
Agenda items are subject to change as
priorities dictate.
Name: Advisory Committee for Injury
Prevention and Control.
Times and Dates: 1 p.m.–5:30 p.m., June
13, 2006. 8:30 a.m.–12 p.m., June 14, 2006.
Place: Doubletree Hotel Atlanta, 3342
Peachtree Road, NE., Atlanta, GA 30326.
Status: Closed: 1 p.m.–1:45 p.m., June 13,
2006. Open: 1:45 p.m.–5:30 p.m., June 13,
2006. Open: 8:30 a.m.–12 p.m., June 14,
2006.
Purpose: The committee advises and makes
recommendations to the Secretary,
Department of Health and Human Services,
the Director, CDC, and the Director, NCIPC,
regarding feasible goals for the prevention
and control of injury. The committee makes
recommendations regarding policies,
VerDate Aug<31>2005
16:29 May 10, 2006
Jkt 208001
strategies, objectives, and priorities, and
reviews progress toward injury prevention
and control.
Matters to be Discussed: From 1 p.m.–1:45
p.m., June 13, 2006 the full committee will
vote on the results of secondary review. This
portion of the meeting will be closed to the
public in accordance with provisions set
forth in section 552(b)(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.
Following the closed session, the meeting
will open to the public.
Agenda items are subject to change as
priorities dictate.
For Further Information Contact: Ms.
Louise Galaska, Executive Secretary, ACIPC,
NCIPC, CDC, 4770 Buford Highway, NE., M/
S K02, Atlanta, Georgia 30341–3724,
telephone (770) 488–4694.
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 CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: May 5, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–7209 Filed 5–10–06; 8:45 am]
(71 FR 7052), the agency announced
that the proposed information collection
had been submitted 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 0910–0183. The
approval expires on April 30, 2009. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.fda.gov/
ohrms/dockets.
Dated: May 4, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–7157 Filed 5–10–06; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N–0157]
BILLING CODE 4163–18–P
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Adverse Drug Experience Reporting
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
Food and Drug Administration
ACTION:
[Docket No. 2005N–0425]
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Adverse Drug Experience Reporting’’
has been approved by the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Karen L. Nelson, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1482.
SUPPLEMENTARY INFORMATION: In the
Federal Register of February 7, 2006 (71
FR 6281), the agency announced that
the proposed information collection had
been submitted 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 0910–0230. The
approval expires on April 30, 2009. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.fda.gov/
ohrms/dockets.
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
General Administrative Procedures:
Citizen Petitions; Petition for
Reconsideration or Stay of Action;
Advisory Opinions
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘General Administrative Procedures:
Citizen Petitions; Petition for
Reconsideration or Stay of Action;
Advisory Opinions’’ 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 Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–4659.
SUPPLEMENTARY INFORMATION: In the
Federal Register of February 10, 2006
PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
Food and Drug Administration,
HHS.
E:\FR\FM\11MYN1.SGM
Notice.
11MYN1
Agencies
[Federal Register Volume 71, Number 91 (Thursday, May 11, 2006)]
[Notices]
[Page 27502]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-7157]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N-0425]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; General Administrative Procedures:
Citizen Petitions; Petition for Reconsideration or Stay of Action;
Advisory Opinions
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``General Administrative Procedures:
Citizen Petitions; Petition for Reconsideration or Stay of Action;
Advisory Opinions'' 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 Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-4659.
SUPPLEMENTARY INFORMATION: In the Federal Register of February 10, 2006
(71 FR 7052), the agency announced that the proposed information
collection had been submitted 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 0910-0183.
The approval expires on April 30, 2009. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.fda.gov/ohrms/dockets.
Dated: May 4, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-7157 Filed 5-10-06; 8:45 am]
BILLING CODE 4160-01-S