Memorandum of Understanding Between the United States Food and Drug Administration and the Veterans Health Administration, 4514-4519 [07-421]
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Federal Register / Vol. 72, No. 20 / Wednesday, January 31, 2007 / Notices
For Further Information Contact:
Demetria Gardner, Immunization
Services Division, National Center for
Immunization and Respiratory Diseases,
CDC, 1600 Clifton Road, NE., (E–05),
Atlanta, Georgia 30333, telephone 404/
639–8836, fax 404/639–6258.
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 CDC
and ATSDR.
Elaine L. Baker,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. E7–1490 Filed 1–30–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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Statement of Organization, Functions,
and Delegations of Authority
Part C (Centers for Disease Control
and Prevention) of the Statement of
Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (45 FR 67772–76, dated
October 14, 1980, and corrected at 45 FR
69296, October 20, 1980, as amended
most recently at 71 FR 69211, dated
November 30, 2006) is amended to
reflect the establishment of the
Extramural Research Program Office
within the National Center for Injury
Prevention and Control, coordinating
Center for Environmental Health and
Injury Prevention.
Section C–B, Organization and
Functions, is hereby amended as
follows: After the functional statement
for the Office of Communication
Resources (CTC14), Office of the
Director (CTC1), National Center for
Injury Prevention and Control (CTC),
insert the following:
Extramural Research Program Office
(CTC16). The Extramural Research
Program Office (ERPO) plans, develops,
coordinates, and evaluates extramural
research activities in cooperation with
centers, divisions, and offices within the
Coordinating Center for Environmental
Health and Injury Prevention. In
carrying out its mission, the ERPO: (1)
Directs the Extramural research program
by planning, coordinating, developing,
implementing, monitoring, and
evaluating extramural research that is
designed to address center priorities; (2)
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participates with divisions and offices
within the center to establish research
priorities for the center; (3) provides
scientific leadership in the areas of
extramural research supported by the
center; (4) promotes and prepares
initiatives to stimulate extramural
research in relevant priority areas; (5)
coordinates and conducts in-depth
external peer review and secondary
program relevance review of extramural
research applications by use of
consultant expert panels; (6) makes
recommendations to the center director
on award selections and staff members
serve as the program officials in
conjunction with CDC grants
management and policy officials to
implement and monitor the scientific,
technical, and administrative aspects of
awards; (7) facilitates scientific
collaborations between external and
internal investigators; (8) disseminates
and evaluates extramural research
progress, findings, and impact; and (9)
assists the Office of Chief Science
Officer, CDC, in developing extramural
research policies and oversees the
implementation of those policies within
the center.
Dated: January 9, 2007.
William H. Gimson,
Chief Operating Officer, Centers for Disease
Control and Prevention (CDC).
[FR Doc. 07–417 Filed 1–30–07; 8:45 am]
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Food and Drug Administration
[Docket No. 2006N–0136]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Interstate Shellfish Dealers Certificate
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Interstate Shellfish Dealers Certificate’’
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 the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4659.
SUPPLEMENTARY INFORMATION: In the
Federal Register of October 13, 2006 (71
PO 00000
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Dated: January 25, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–1549 Filed 1–30–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FDA 225–07–4300]
Memorandum of Understanding
Between the United States Food and
Drug Administration and the Veterans
Health Administration
AGENCY:
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Food and Drug Administration,
HHS.
ACTION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
FR 60545), 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 0910–0021. The
approval expires on January 31, 2010. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.fda.gov/
ohrms/dockets.
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is providing
notice of a memorandum of
understanding (MOU) between FDA and
the Veterans Health Administration.
The purpose of this MOU is to enhance
knowledge and efficiency by providing
for the sharing of information and
expertise related to the review and use
of FDA-regulated drugs, biologics, and
medical devices between the two
agencies. The goals of the collaboration
are to explore ways to: Further enhance
information sharing efforts through
more efficient and robust interagency
activities; promote efficient utilization
of tools and expertise for product risk
identification, validation, and analysis;
and build infrastructure and processes
that meet the common needs for
evaluating the safety, efficacy, and
utilization of drugs, biologics, and
medical devices.
DATES: The agreement became effective
January 23, 2007.
FOR FURTHER INFORMATION CONTACT:
Jeffrey Shuren, Office of Policy (HF–11),
Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857,
301–827–3360.
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Federal Register / Vol. 72, No. 20 / Wednesday, January 31, 2007 / Notices
In
accordance with 21 CFR 20.108(c),
which states that all written agreements
and MOUs between FDA and others
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SUPPLEMENTARY INFORMATION:
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shall be published in the Federal
Register, the agency is publishing notice
of this MOU.
PO 00000
Dated: January 25, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
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[FR Doc. 07–421 Filed 1–30–07; 8:45 am]
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]]>Agencies
[Federal Register Volume 72, Number 20 (Wednesday, January 31, 2007)]
[Notices]
[Pages 4514-4519]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-421]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[FDA 225-07-4300]
Memorandum of Understanding Between the United States Food and
Drug Administration and the Veterans Health Administration
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is providing notice of
a memorandum of understanding (MOU) between FDA and the Veterans Health
Administration. The purpose of this MOU is to enhance knowledge and
efficiency by providing for the sharing of information and expertise
related to the review and use of FDA-regulated drugs, biologics, and
medical devices between the two agencies. The goals of the
collaboration are to explore ways to: Further enhance information
sharing efforts through more efficient and robust interagency
activities; promote efficient utilization of tools and expertise for
product risk identification, validation, and analysis; and build
infrastructure and processes that meet the common needs for evaluating
the safety, efficacy, and utilization of drugs, biologics, and medical
devices.
DATES: The agreement became effective January 23, 2007.
FOR FURTHER INFORMATION CONTACT: Jeffrey Shuren, Office of Policy (HF-
11), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD
20857, 301-827-3360.
[[Page 4515]]
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 20.108(c), which
states that all written agreements and MOUs between FDA and others
shall be published in the Federal Register, the agency is publishing
notice of this MOU.
Dated: January 25, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
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[FR Doc. 07-421 Filed 1-30-07; 8:45 am]
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