Federal Register / Vol. 73, No.
18 / Monday, January 28, 2008 / Notices
welfare cases; and (2) Training judges,
attorneys, and other legal personnel in
child welfare cases; and conducting
cross-training with child welfare agency
staff and contractors.
The statute requires separate
applications for these two new grants.
The annual burden estimates below
describe the estimated burden for the
two new grants. ACF collects
Application .......................................................................................................
Annual Program Report ...................................................................................
Estimated Total Annual Burden
Hours: 7,904.
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: January 18, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. 08–324 Filed 1–25–08; 8:45 am]
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4873
information from the States about their
work under these grants (applications,
program reports) by way of a Program
Instruction issued on June 15, 2006.
This Program Instruction describes
the programmatic and fiscal provisions
and reporting requirements for each of
the grants, specifies the application
submittal and approval procedures for
the grants for fiscal years 2006 through
ANNUAL BURDEN ESTIMATES
Number of re-
Instrument
spondents
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Awards to Eleven Office of Refugee
Resettlement Shelter Care Providers
AGENCY: Office of Refugee Resettlement,
Administration for Children and
Families, HHS.
ACTION: Notice of Grant Awards.
CFDA #: 93.676
SUMMARY: This notice is hereby given
that an award will be made to an
unaccompanied alien shelter care
provider, Southwest Regional Youth
Village, Vincennes, Indiana, in the
amount of $586,719. This funding will
support services through September 30,
2008.
This funding will support the
expansion of secure program bed
capacity to meet the number of
unaccompanied alien children referrals
from the Department of Homeland
Security (DHS).
The program is mandated by section
462 of the Homeland Security Act to
ensure appropriate placement of all
referrals from the DHS. ORR’s ability to
meet this mandate is often a challenge
since the program is completely tied to
DHS interior apprehension strategies
and the sporadic number of border
crossers.
The program has very specific
requirements for the provision of
services. This grantee is one of the only
entities with the infrastructure,
licensing, experience and appropriate
level of trained staff to meet the service
requirements for secure capacity. The
program’s ability to meet the number of
secure referrals from DHS can only be
accommodated through the expansion
Jkt 214001 PO 00000 Frm 00107 Fmt 4703 Sfmt 4703
2010, and identifies technical resources
for use by State courts during the course
of the grants. The agency uses the
information received to ensure
compliance with the statute and provide
training and technical assistance to the
grantees.
Respondents: State Courts.
Number of re- Average bur-
Total burden
sponses per den hours per
hours
respondent response
52 2 40 4,160
52 2 36 3,744
of this program through the
supplemental award process.
FOR FURTHER INFORMATION CONTACT:
Kenneth Tota, Office of Refugee
Resettlement, Administration for
Children and Families, 370 L’Enfant
Promenade, SW., Washington, DC,
20447, telephone (202) 401–4858.
Dated: January 17, 2008.
Brent Orrell,
Acting Director, Office of Refugee
Resettlement.
[FR Doc. E8–1360 Filed 1–25–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2008N–0019]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Survey of Food Safety and Nutrition
Information Provided to Pregnant
Women by Health Care Providers and
the Special Supplemental Nutrition
Program for Women, Infants, and
Children Educators
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Survey of Food Safety and Nutrition
Information Provided to Pregnant
Women by Health Care Providers and
WIC Educators’’ 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
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 4874 Federal Register / Vol. 73, No. 18 / Monday, January 28, 2008 / Notices
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4659.
SUPPLEMENTARY INFORMATION: In the
Federal Register of March 20, 2007 (72
FR 13117), 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 0910–0617. The
approval expires on January 31, 2011. A
copy of the supporting statement for this
information collection is available on
the Internet at http://www.reginfo.gov/
public/do/PRAMain.
Dated: January 18, 2008.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E8–1353 Filed 1–25–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2008N–0018]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Food and Drug Administration Survey
of Physicians’ Perceptions of the
Impact of Early Risk Communication
About Medical Products
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘FDA Survey of Physicians’ Perceptions
of the Impact of Early Risk
Communication About Medical
Products’’ 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–
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4659.
SUPPLEMENTARY INFORMATION: In the
Federal Register of July 19, 2007 (72 FR
39628), the agency announced that the
proposed information collection had
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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 0910–0615. The
approval expires on December 31, 2010.
A copy of the supporting statement for
this information collection is available
on the Internet at http://
www.reginfo.gov/public/do/PRAMain.
Dated: January 18, 2008.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E8–1355 Filed 1–25–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2008N–0017]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Exports:
Notification and Recordkeeping
Requirements
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the notification and recordkeeping
requirements for persons exporting
human drugs, biological products,
devices, animal drugs, food, and
cosmetics that may not be marketed or
sold in the United States.
DATES: Submit written or electronic
comments on the collection of
information by March 28, 2008.
ADDRESSES: Submit electronic
comments on the collection of
information to: http://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
PO 00000 Frm 00108 Fmt 4703 Sfmt 4703
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
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: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60–day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Exports: Notification and
Recordkeeping Requirements, 21 CFR
Part 1 (OMB Control Number 0910–
0482) — Extension
The respondents to this information
collection are exporters who have
notified FDA of their intent to export
unapproved products that may not be
sold or marketed in the United States as
allowed under 801(e) of the Federal
Food, Drug, and Cosmetic Act (the act)
(21 U.S.C. 381). In general, the
notification identifies the product being
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