Tobacco Products Scientific Advisory Committee; Notice of Meeting, 76993 [2010-31066]
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Federal Register / Vol. 75, No. 237 / Friday, December 10, 2010 / Notices
requirements of the applicable statutes
and regulations.
II. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) either electronic or written
comments regarding this document. It is
only necessary to send one set of
comments. It is no longer necessary to
send two copies of mailed comments.
Identify comments 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.
III. Electronic Access
Persons with access to the Internet
may obtain the guidance at https://
www.fda.gov/oc/advisory/default.htm.
Dated: December 6, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–31022 Filed 12–9–10; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0001]
Tobacco Products Scientific Advisory
Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
mstockstill on DSKH9S0YB1PROD with NOTICES
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Tobacco Products
Scientific Advisory Committee.
General Function of the Committee: To
provide advice and recommendations to the
Agency on FDA’s regulatory issues.
Date and Time: The meeting will be held
on January 10 and 11, 2011 from 8 a.m. until
5 p.m.
Location: FDA White Oak Conference
Center, Bldg. 31, rm. 1503, 10903 New
Hampshire Ave., Silver Spring, MD 20993–
0002. Information regarding special
accommodations due to a disability, visitor
parking and transportation may be accessed
at: https://www.fda.gov/AdvisoryCommittees/
default.htm; under the heading ‘‘Resources
for You,’’ click on ‘‘White Oak Conference
Center Parking and Transportation
Information for FDA Advisory Committee
Meetings.’’ Please note that visitors to the
White Oak Campus must have a valid
driver’s license or other picture ID, and must
enter through Building 1.
VerDate Mar<15>2010
18:39 Dec 09, 2010
Jkt 223001
Contact Person: Caryn Cohen, Office of
Science, Center for Tobacco Products, Food
and Drug Administration, 9200 Corporate
Blvd., Rockville, MD 20850, 1–877–287–1373
(choose Option 4), e-mail:
TPSAC@fda.hhs.gov, or FDA Advisory
Committee Information Line, 1–800–741–
8138 (301–443–0572 in the Washington, DC
area), code 8732110002. Please call the
Information Line for up-to-date information
on this meeting. A notice in the Federal
Register about last minute modifications that
impact a previously announced advisory
committee meeting cannot always be
published quickly enough to provide timely
notice. Therefore, you should always check
the Agency’s Web site and call the
appropriate advisory committee hot line/
phone line to learn about possible
modifications before coming to the meeting.
Agenda: On January 10 and 11, 2011, the
Committee will continue to (1) receive
updates from the Menthol Report
Subcommittee and (2) receive and discuss
presentations regarding the data requested by
the Committee at the March 30 and 31, 2010,
meeting of the Tobacco Products Scientific
Advisory Committee.
FDA intends to make background material
available to the public no later than 2
business days before the meeting. If FDA is
unable to post the background material on its
Web site prior to the meeting, the background
material will be made publicly available at
the location of the advisory committee
meeting, and the background material will be
posted on FDA’s Web site after the meeting.
Background material is available at https://
www.fda.gov/AdvisoryCommittees/Calendar/
default.htm. Scroll down to the appropriate
advisory committee link.
Procedure: Interested persons may present
data, information, or views, orally or in
writing, on issues pending before the
committee. Written submissions may be
made to the contact person on or before
December 30, 2010. Oral presentations from
the public will be scheduled between
approximately 3 p.m. and 4 p.m. on January
10, 2011. Those individuals interested in
making formal oral presentations should
notify the contact person and submit a brief
statement of the general nature of the
evidence or arguments they wish to present,
the names and addresses of proposed
participants, and an indication of the
approximate time requested to make their
presentation on or before December 21, 2010.
Time allotted for each presentation may be
limited. If the number of registrants
requesting to speak is greater than can be
reasonably accommodated during the
scheduled open public hearing session, FDA
may conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by December 22, 2010.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee meetings
and will make every effort to accommodate
persons with physical disabilities or special
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
76993
needs. If you require special accommodations
due to a disability, please contact Caryn
Cohen at least 7 days in advance of the
meeting.
FDA is committed to the orderly conduct
of its advisory committee meetings. Please
visit our Web site at https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/ucm111462.htm
for procedures on public conduct during
advisory committee meetings.
Notice of this meeting is given under the
Federal Advisory Committee Act (5 U.S.C.
app. 2).
Dated: December 3, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–31066 Filed 12–9–10; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
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Comment Request; Generic Clearance
for Surveys of Customers and Partners
of the Office of Extramural Research of
the National Institutes of Health
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of
Extramural Research (OER), the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below. This proposed
information collection was previously
published in the Federal Register on
September 13, 2010 (Volume 75,
Number 176, page 55585) and allowed
60 days for public comment. One public
comment was received. The purpose of
this notice is to allow an additional 30
days for public comment. The National
Institutes of Health may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
Proposed Collection: Title: Generic
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from partners and customers is
SUMMARY:
E:\FR\FM\10DEN1.SGM
10DEN1
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[Federal Register Volume 75, Number 237 (Friday, December 10, 2010)]
[Notices]
[Page 76993]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-31066]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0001]
Tobacco Products Scientific Advisory Committee; Notice of Meeting
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
This notice announces a forthcoming meeting of a public advisory
committee of the Food and Drug Administration (FDA). The meeting will
be open to the public.
Name of Committee: Tobacco Products Scientific Advisory
Committee.
General Function of the Committee: To provide advice and
recommendations to the Agency on FDA's regulatory issues.
Date and Time: The meeting will be held on January 10 and 11,
2011 from 8 a.m. until 5 p.m.
Location: FDA White Oak Conference Center, Bldg. 31, rm. 1503,
10903 New Hampshire Ave., Silver Spring, MD 20993-0002. Information
regarding special accommodations due to a disability, visitor
parking and transportation may be accessed at: https://www.fda.gov/AdvisoryCommittees/default.htm; under the heading ``Resources for
You,'' click on ``White Oak Conference Center Parking and
Transportation Information for FDA Advisory Committee Meetings.''
Please note that visitors to the White Oak Campus must have a valid
driver's license or other picture ID, and must enter through
Building 1.
Contact Person: Caryn Cohen, Office of Science, Center for
Tobacco Products, Food and Drug Administration, 9200 Corporate
Blvd., Rockville, MD 20850, 1-877-287-1373 (choose Option 4), e-
mail: TPSAC@fda.hhs.gov, or FDA Advisory Committee Information Line,
1-800-741-8138 (301-443-0572 in the Washington, DC area), code
8732110002. Please call the Information Line for up-to-date
information on this meeting. A notice in the Federal Register about
last minute modifications that impact a previously announced
advisory committee meeting cannot always be published quickly enough
to provide timely notice. Therefore, you should always check the
Agency's Web site and call the appropriate advisory committee hot
line/phone line to learn about possible modifications before coming
to the meeting.
Agenda: On January 10 and 11, 2011, the Committee will continue
to (1) receive updates from the Menthol Report Subcommittee and (2)
receive and discuss presentations regarding the data requested by
the Committee at the March 30 and 31, 2010, meeting of the Tobacco
Products Scientific Advisory Committee.
FDA intends to make background material available to the public
no later than 2 business days before the meeting. If FDA is unable
to post the background material on its Web site prior to the
meeting, the background material will be made publicly available at
the location of the advisory committee meeting, and the background
material will be posted on FDA's Web site after the meeting.
Background material is available at https://www.fda.gov/AdvisoryCommittees/Calendar/default.htm. Scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may present data, information, or
views, orally or in writing, on issues pending before the committee.
Written submissions may be made to the contact person on or before
December 30, 2010. Oral presentations from the public will be
scheduled between approximately 3 p.m. and 4 p.m. on January 10,
2011. Those individuals interested in making formal oral
presentations should notify the contact person and submit a brief
statement of the general nature of the evidence or arguments they
wish to present, the names and addresses of proposed participants,
and an indication of the approximate time requested to make their
presentation on or before December 21, 2010. Time allotted for each
presentation may be limited. If the number of registrants requesting
to speak is greater than can be reasonably accommodated during the
scheduled open public hearing session, FDA may conduct a lottery to
determine the speakers for the scheduled open public hearing
session. The contact person will notify interested persons regarding
their request to speak by December 22, 2010.
Persons attending FDA's advisory committee meetings are advised
that the Agency is not responsible for providing access to
electrical outlets.
FDA welcomes the attendance of the public at its advisory
committee meetings and will make every effort to accommodate persons
with physical disabilities or special needs. If you require special
accommodations due to a disability, please contact Caryn Cohen at
least 7 days in advance of the meeting.
FDA is committed to the orderly conduct of its advisory
committee meetings. Please visit our Web site at https://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees/ucm111462.htm for
procedures on public conduct during advisory committee meetings.
Notice of this meeting is given under the Federal Advisory
Committee Act (5 U.S.C. app. 2).
Dated: December 3, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-31066 Filed 12-9-10; 8:45 am]
BILLING CODE 4160-01-P