Risk Communication Advisory Committee; Notice of Meeting, 57279-57280 [2010-23368]
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57279
Federal Register / Vol. 75, No. 181 / Monday, September 20, 2010 / Notices
The response burden for service
providers is estimated as:
Number of
respondents
Component
Provider Report ................................................
Component
Electronic data
system
Client Report ....................
Responses per
provider
2,080*
Number of
respondents
Hours per
response
Total responses
1
Responses per
provider
2,080*
Total burden
hours
2.30
Hours per
response
Total responses
4,784
Total burden
hours
56
1,822
1
1
56
1,822
106.25
3.75
5,950
6,832.5
Subtotal
* All
No
Yes
**1,878
............................
**1,878
............................
12,782.5
providers, including providers of administrative support services and direct client services.
of direct client services only.
** Providers
Total Burden Hours: 17,974.5
E-mail comments to
paperwork@hrsa.gov or mail comments
to the HRSA Reports Clearance Officer,
Room 10–33, Parklawn Building, 5600
Fishers Lane, Rockville, Maryland,
20857. Written comments should be
received within 60-days of this notice.
Information can also be accessed at
https://datasupport.hab.hrsa.gov/.
Dated: September 14, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–23416 Filed 9–17–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Request for State Data Needed to
Determine Amount of a Tribal Family
Assistance Grant.
OMB No.: 0970–0173.
Description: 42 U.S.C. 612 (Section
412 of the Social Security Act) gives
Federally recognized Indian Tribes the
opportunity to apply to operate a Tribal
Temporary Assistance for Needy
Families (TANF) program. The Act
specifies that the Secretary shall use
State-submitted data to determine the
amount of the grant to the Tribe. This
form (letter) is used to request those
data from the States. ACF is proposing
to extend this information collection
without change.
Respondents: States that have Indian
Tribes applying to operate a TANF
program.
ANNUAL BURDEN ESTIMATES
Information collection
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
Total burden
hours
Request for State Data Needed to Determine the Amount of Tribal Family
Assistance Grant ..........................................................................................
4
1
42
168
Total Estimated Burden: 168 hours.
jdjones on DSK8KYBLC1PROD with NOTICES
Additional Information
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. E-mail address:
infocollection@acf.hhs.gov.
OMB Comment
OMB is required to make a decision
concerning the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication. Written comments and
VerDate Mar<15>2010
15:00 Sep 17, 2010
Jkt 220001
recommendations for the proposed
information collection should be sent
directly to the following:
Office of Management and Budget,
Paperwork Reduction Project. Fax: 202–
395–7285. E-mail:
OIRA_SUBMISSION@OMB.EOP.GOV.
Attn: Desk Officer for the
Administration for Children and
Families.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: September 13, 2010.
Robert Sargis,
Reports Clearance Officer.
ACTION:
[FR Doc. 2010–23319 Filed 9–17–10; 8:45 am]
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Food and Drug Administration
[Docket No. FDA–2010–N–0001]
Risk Communication Advisory
Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
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: Risk
Communication Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
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jdjones on DSK8KYBLC1PROD with NOTICES
57280
Federal Register / Vol. 75, No. 181 / Monday, September 20, 2010 / Notices
Date and Time: The meeting will be
held on November 8, 2010, from 8 a.m.
to 5 p.m. and November 9, 2010, from
8 a.m. to 2 p.m.
Location: FDA White Oak Campus,
Building 31 Conference Center, Great
Room, 10903 New Hampshire Ave.,
Silver Spring, MD 20993. Please note
visitors can park in the southwest garage
near Building 31 or the northwest
parking lot near Building 22 (for a
campus map, see https://www.fda.gov/
downloads/AboutFDA/WorkingatFDA/
BuildingsandFacilities/WhiteOak
CampusInformation/UCM194893.pdf).
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: Lee L. Zwanziger,
Office of Policy, Planning and
Preparedness, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, rm. 3278, Silver Spring,
MD, 20993, 301–796–9151, FAX: 301–
847–8611, e-mail: RCAC@fda.hhs.gov,
or FDA Advisory Committee
Information Line, 1–800–741–8138
(301–443–0572 in the Washington, DC
area), code 8732112560. 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 November 8 and 9, 2010,
the Committee will hear and discuss
developments in FDA’s ongoing
communications programs, such as
FDA’s Strategic Plan for Risk
Communication, FDA’s Transparency
Initiative, and the challenges of
effectively communicating with patients
and caregivers about appropriate use of
medical devices when a patient is
prescribed a medical device for home
use.
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/
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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 October 29, 2010.
Oral presentations from the public will
be scheduled between approximately 1
p.m. and 2 p.m. on November 8, 2010,
and 10:30 to 11:30 a.m. on November 9,
2010. Those desiring to make 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 October 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
October 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 Lee
Zwanziger 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/AboutAdvisory
Committees/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: September 14, 2010.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
[FR Doc. 2010–23368 Filed 9–17–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Environmental
Health Sciences; Notice of Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the Board
of Scientific Counselors, NIEHS.
The meeting will be open to the
public as indicated below, 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.
The meeting will be closed to the
public as indicated below in accordance
with the provisions set forth in section
552b(c)(6), Title 5 U.S.C., as amended
for the review, discussion, and
evaluation of individual intramural
programs and projects conducted by the
NATIONAL INSTITUTE OF
ENVIRONMENTAL HEALTH
SCIENCES, including consideration of
personnel qualifications and
performance, and the competence of
individual investigators, the disclosure
of which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Board of Scientific
Counselors, NIEHS.
Date: October 17–19, 2010.
Closed: October 17, 2010, 7 p.m. to 10 p.m
Agenda: To review and evaluate
programmatic and personnel issues.
Place: Doubletree Guest Suites, 2515
Meridian Parkway, Research Triangle Park,
NC 27713.
Open: October 18, 2010, 8:30 a.m. to 11:50
a.m.
Agenda: An overview of the organization
and research in the Laboratory of
Reproductive and Developmental
Toxicology.
Place: Nat. Inst. of Environmental Health
Sciences, Building 101, Rodbell Auditorium,
111 T. W. Alexander Drive, Conference
Rooms 101 A, B, and C, Research Triangle
Park, NC 27709.
Closed: October 18, 2010, 11:50 a.m. to
12:35 p.m.
Agenda: To review and evaluate
programmatic and personnel issues.
Place: Nat. Inst. of Environmental Health
Sciences, Building 101, Rodbell Auditorium,
111 T. W. Alexander Drive, Conference
Rooms 101 A, B, and C, Research Triangle
Park, NC 27709.
Open: October 18, 2010, 1:30 p.m. to 2:45
p.m.
Agenda: An overview of the organization
and research in the Laboratory of
Reproductive and Developmental
Toxicology.
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Agencies
[Federal Register Volume 75, Number 181 (Monday, September 20, 2010)]
[Notices]
[Pages 57279-57280]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-23368]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0001]
Risk Communication 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: Risk Communication Advisory Committee.
General Function of the Committee: To provide advice and
recommendations to the agency on FDA's regulatory issues.
[[Page 57280]]
Date and Time: The meeting will be held on November 8, 2010, from 8
a.m. to 5 p.m. and November 9, 2010, from 8 a.m. to 2 p.m.
Location: FDA White Oak Campus, Building 31 Conference Center,
Great Room, 10903 New Hampshire Ave., Silver Spring, MD 20993. Please
note visitors can park in the southwest garage near Building 31 or the
northwest parking lot near Building 22 (for a campus map, see https://www.fda.gov/downloads/AboutFDA/WorkingatFDA/BuildingsandFacilities/WhiteOakCampusInformation/UCM194893.pdf). 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: Lee L. Zwanziger, Office of Policy, Planning and
Preparedness, Food and Drug Administration, 10903 New Hampshire Ave.,
Bldg. 32, rm. 3278, Silver Spring, MD, 20993, 301-796-9151, FAX: 301-
847-8611, e-mail: RCAC@fda.hhs.gov, or FDA Advisory Committee
Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC
area), code 8732112560. 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 November 8 and 9, 2010, the Committee will hear and
discuss developments in FDA's ongoing communications programs, such as
FDA's Strategic Plan for Risk Communication, FDA's Transparency
Initiative, and the challenges of effectively communicating with
patients and caregivers about appropriate use of medical devices when a
patient is prescribed a medical device for home use.
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
October 29, 2010. Oral presentations from the public will be scheduled
between approximately 1 p.m. and 2 p.m. on November 8, 2010, and 10:30
to 11:30 a.m. on November 9, 2010. Those desiring to make 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 October 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 October
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 Lee Zwanziger 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: September 14, 2010.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
[FR Doc. 2010-23368 Filed 9-17-10; 8:45 am]
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