Federal Register / Vol. 72, No.
117 / Tuesday, June 19, 2007 / Notices
self-sufficiency services for parents,
parent skills training, and high-quality
child care for children in low-income
families in Kansas and Missouri.
The purpose of the current document
is to request public comment on the 36-
month participant survey in
Philadelphia. The research team plans
to collect participant-reported surveys
assessing participants’ employment,
education and economic outcomes,
participation in employment and
training services, receipt of benefits and
services such as food stamps and mental
health services, housing and household
information, health and health care
coverage, child care, and child
outcomes.
The follow-up survey at the 36-month
follow-up in Philadelphia will be used
for the following purposes: To study the
Philadelphia 36-month participant survey ........................................................
Estimated Total Annual Burden
Hours: 1,166.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded 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. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
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Request for State Data Needed to Determine the Amount of a Tribal Family
Assistance Grant ..........................................................................................
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33763
extent to which pre-employment
services and transitional employment
affect employment, earnings, income,
and welfare dependence of low-income
TANF recipients; to examine the
impacts of these services on
participants’ health, receipt of benefits
such as food stamps, Medicaid, and
child-care subsidies, and participation
in services such as substance abuse
treatment and mental health services;
and to collect data on a wider range of
outcomes measures than is available
through welfare, Medicaid, Food
Stamps, Social Security, and
Unemployment Insurance records.
The 36-month data collection effort
draws heavily from the 15-month survey
conducted in this site. Materials for the
15-month data collection effort were
ANNUAL BURDEN ESTIMATES
Number of
Instrument
respondents
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Dated: June 13, 2007.
Brendan Kelly,
OPRE Reports Clearance Officer.
[FR Doc. 07–2998 Filed 6–18–07; 8:45 am]
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ANNUAL BURDEN ESTIMATES
Number of
Instrument
respondents
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previously submitted to OMB and were
approved (OMB Control No. 0970–
0276).
Respondents: TANF recipients
without a high school diploma and/or
recipients who have received TANF for
at least 12 months.
The fielded sample of the 36-month
data collection effort will be all 1,944
participants in the two program groups
and the control group of the HtE project
in Philadelphia. The burden estimates
below assume an 80 percent response
rate of the fielded sample.
The annual burden estimates are
detailed below, and the substantive
content of each component will be
detailed in the supporting statement
attached to the forthcoming 30-day
notice.
Number of Average
Total burden
responses per burden hours
hours
respondent per response
1,555 1 0.75 1,166
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Request for State Data Needed to
Determine the 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 TANIF
program.
Number of Average
Total burden
responses per burden hours
hours
respondent per response
15 1 42 630
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 33764 Federal Register / Vol. 72, No. 117 / Tuesday, June 19, 2007 / Notices
Estimated Total Annual Burden
Hours: 630.
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 recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, FAX: 202–395–6974,
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: June 14, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07–3004 Filed 6–18–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Cellular, Tissue, and Gene Therapies
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). At least one portion of the
meeting will be closed to the public.
Name of Committee: Cellular, Tissue,
and Gene Therapies 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 by teleconference on July 26, 2007
from 11 a.m. to approximately 3:15 p.m.
Location: National Institutes of
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Health, Bldg. 29B, Conference rms. A/B,
9000 Rockville Pike, Bethesda, MD. This
meeting will be held by teleconference.
The public is welcome to attend the
meeting at the specified location. A
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speakerphone will be provided at the
specified location for public
participation in the meeting. Important
information about transportation and
directions to the NIH campus, parking,
and security procedures is available on
the Internet at http://www.nih.gov/
about/visitor/index.htm. Visitors must
show two forms of identification, one of
which must be a government-issued
photo identification such as a Federal
employee badge, driver’s license,
passport, green card, etc. If you are
planning to drive to and park on the
NIH campus, you must enter at the
South Dr. entrance of the campus which
is located on Wisconsin Ave. (the
Medical Center Metro entrance), and
allow extra time for vehicle inspection.
Detailed information about security
procedures is located at http://
www.nih.gov/about/visitorsecurity.htm.
Due to the limited available parking,
visitors are encouraged to use public
transportation.
Contact Person: Gail Dapolito or
Danielle Cubbage, Center for Biologics
Evaluation and Research, Food and
Drug Administration, 1401 Rockville
Pike, Rockville, MD, 20852, 301–827–
0314, or FDA Advisory Committee
Information Line, 1–800–741–8138
(301–443–0572 in the Washington, DC
area), code 3014512389. 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 July 26, 2007, the
committee will meet in open session to
hear updates of research programs in:
(1) The Division of Therapeutic Proteins
and the Division of Monoclonal
Antibodies, Office of Biotechnology
Products, Center for Drug Evaluation
and Research, FDA and (2) the Division
of Cellular and Gene Therapies, Office
of Cellular, Tissue, and Gene Therapies,
Center for Biologics Evaluation and
Research, FDA.
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
PO 00000 Frm 00030 Fmt 4703 Sfmt 4703
the meeting. Background material is
available at http://www.fda.gov/ohrms/
dockets/ac/acmenu.htm, click on the
year 2007 and scroll down to the
appropriate advisory committee link.
Procedure: On July 26, 2007, from 11
a.m. to approximately 2 p.m., the
meeting is open to the public. 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 July 12, 2007. Oral
presentations from the public will be
scheduled between approximately 1
p.m. and 2 p.m. 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 July 18, 2007. 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 July 19, 2007.
Closed Committee Deliberations: On
July 26, 2007, from approximately 2:15
p.m. to 3:30 p.m., the meeting will be
closed to permit discussion where
disclosure would constitute a clearly
unwarranted invasion of personal
privacy (5 U.S.C. 552b(c)(6)). The
committee will discuss reports of
intramural research programs and make
recommendations regarding personnel
staffing decisions.
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 Gail Dapolito
at least 7 days in advance of the
meeting.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: June 11, 2007.
Randall W. Lutter,
Associate Commissioner for Policy and
Planning.
[FR Doc. E7–11728 Filed 6–18–07; 8:45 am]
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