Center for Scientific Review; Notice of Meeting, 61693 [E9-28287]
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Federal Register / Vol. 74, No. 226 / Wednesday, November 25, 2009 / Notices
I. Background
FDA is announcing the availability of
a guidance for industry entitled
‘‘Residual Solvents in Drug Products
Marketed in the United States.’’ On
August 7, 2008 (73 FR 46020), FDA
announced the availability of the draft
version of this guidance. The public
comment period closed on October 6,
2008. A number of comments were
received, which the agency considered
carefully as it finalized the guidance. In
response to the comments, FDA made
appropriate changes. The guidance
provides information on how new drug
application (NDA) and abbreviated new
drug application (ANDA) applicants for
noncompendial drug products should
limit residual solvents as described in
the International Conference on
Harmonisation guidance for industry
‘‘Q3C Impurities: Residual Solvents;’’
how manufacturers of compendial drug
products that are not marketed under an
approved NDA or ANDA can comply
with the new General Chapter <467>
and the Federal Food, Drug, and
Cosmetic Act; and how holders of NDAs
or ANDAs for compendial drug
products should report changes in
chemistry, manufacturing, and controls
specifications to FDA to comply with
the USP General Chapter <467>
‘‘Residual Solvents’’ and § 314.70 (21
CFR 314.70).
This guidance is being issued
consistent with FDA’s good guidance
practices regulation (21 CFR 10.115).
The guidance represents the agency’s
current thinking on USP General
Chapter <467> ‘‘Residual Solvents.’’ It
does not create or confer any rights for
or on any person and does not operate
to bind FDA or the public. An
alternative approach may be used if
such approach satisfies the
requirements of the applicable statutes
and regulations.
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II. The Paperwork Reduction Act of
1995
This guidance refers to previously
approved collections of information
found in FDA regulations. These
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520). Information submitted in the
chemistry, manufacturing, and controls
section of an application under 21 CFR
314.50(d)(1), as well as in amendments
to pending applications under 21 CFR
314.60, is approved by OMB under
Control Number 0910–0001.
Information submitted in an annual
report under § 314.70(d)(2)(i) and (d)(3)
is approved by OMB under Control
VerDate Nov<24>2008
17:36 Nov 24, 2009
Jkt 220001
61693
Number 0910–0001. Recordkeeping
required under 21 CFR 211.165(e) and
211.194(a)(2) is approved by OMB
under Control Number 0910–0139.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
III. Comments
Center for Scientific Review; Notice of
Meeting
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) written or electronic
comments regarding this document.
Submit a single copy of electronic
comments or two paper copies of any
mailed comments, except that
individuals may submit one paper copy.
Comments are to be identified with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
IV. Electronic Access
Persons with access to the Internet
may obtain the document at either
https://www.fda.gov/Drugs/Guidance
ComplianceRegulatoryInformation/
Guidances/default.htm or https://
www.regulations.gov.
Dated: November 19, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9–28247 Filed 11–24–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Cancer Institute; Amended
Notice of Meeting
Notice is hereby given of a change in
the meeting of the National Cancer
Advisory Board, November 30, 2009,
6:30 p.m. to December 2, 2009, 12 p.m.,
National Institutes of Health, Building
31, 31 Center Drive, 10, Bethesda, MD,
20892 which was published in the
Federal Register on November 4, 2009,
74FR57182.
This Federal Register Notice is being
amended to reflect the change in the
start and end times of the closed session
on December 1, 2009 to 3:45 p.m. to
4:30 p.m.
Dated: November 19, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–28279 Filed 11–24–09; 8:45 am]
National Institutes of Health
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
National Institutes of Health Peer
Review Advisory Committee.
The meeting will be open to the
public, with attendance limited to space
available. Individuals who plan to
attend and need special assistance, such
as sign language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
Name of Committee: National Institutes of
Health Peer Review Advisory Committee.
Date: February 1, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: Provide technical and scientific
advice and recommendations to the NIH
Director, the Deputy Director for Extramural
Research, and the Director of the Center for
Scientific Review (CSR) on all procedures
and policies related to the process of peer
review by which the scientific and technical
merit of NIH grant applications is assessed.
Place: Bethesda North Marriott Hotel &
Conference Center, Montgomery County
Conference Center Facility, 5701 Marinelli
Road, North Bethesda, MD 20852.
Contact Person: Cheryl A. Kitt, PhD, Center
for Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3030,
MSC 7776, Bethesda, MD 20892, 301–435–
1112, kittc@csr.nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: November 17, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–28287 Filed 11–24–09; 8:45 am]
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Agencies
[Federal Register Volume 74, Number 226 (Wednesday, November 25, 2009)]
[Notices]
[Page 61693]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-28287]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of Meeting
Pursuant to section 10(a) of the Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is hereby given of a meeting of the
National Institutes of Health Peer Review Advisory Committee.
The meeting will be open to the public, with attendance limited to
space available. Individuals who plan to attend and need special
assistance, such as sign language interpretation or other reasonable
accommodations, should notify the Contact Person listed below in
advance of the meeting.
Name of Committee: National Institutes of Health Peer Review
Advisory Committee.
Date: February 1, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: Provide technical and scientific advice and
recommendations to the NIH Director, the Deputy Director for
Extramural Research, and the Director of the Center for Scientific
Review (CSR) on all procedures and policies related to the process
of peer review by which the scientific and technical merit of NIH
grant applications is assessed.
Place: Bethesda North Marriott Hotel & Conference Center,
Montgomery County Conference Center Facility, 5701 Marinelli Road,
North Bethesda, MD 20852.
Contact Person: Cheryl A. Kitt, PhD, Center for Scientific
Review, National Institutes of Health, 6701 Rockledge Drive, Room
3030, MSC 7776, Bethesda, MD 20892, 301-435-1112, kittc@csr.nih.gov.
Any interested person may file written comments with the
committee by forwarding the statement to the Contact Person listed
on this notice. The statement should include the name, address,
telephone number and when applicable, the business or professional
affiliation of the interested person.
(Catalogue of Federal Domestic Assistance Program Nos. 93.306,
Comparative Medicine; 93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393-93.396, 93.837-93.844, 93.846-93.878, 93.892, 93.893,
National Institutes of Health, HHS)
Dated: November 17, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory Committee Policy.
[FR Doc. E9-28287 Filed 11-24-09; 8:45 am]
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