Submission for OMB Review; Comment Request, 24598-24599 [E8-9762]
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Federal Register / Vol. 73, No. 87 / Monday, May 5, 2008 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: State Plan for Child Support
under Title IV–D of the Social Security
Act (OCSE–100 and OCSE–21–U4).
OMB No.: 0970–0017.
Description: The State plan preprint
pages and amendments serve as a
contract between the Office of Child
Support Enforcement and State and
Territory IV–D agencies. These State
plan preprint pages and amendments
outline the activities States and
Territories will perform as required by
law, in Section 454 of the Social
Security Act, in order for States and
Territories to receive Federal funds to
meet the costs of child support
enforcement.
Respondents: State and Territory IV–
D Agencies.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
State Plan (OCSE–100) ..................................................................................
OCSE–21–U4 ..................................................................................................
Estimated Total Annual Burden
Hours: 324.
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
Number of
responses per
respondent
54
54
Administration for Children and
Families.
Dated: April 28, 2008.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. E8–9751 Filed 5–2–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Reunification Procedures for
Unaccompanied Alien Children.
OMB No.: 0970–0278.
Description: Following the passage of
the 2002 Homeland Security Act (Pub.
L. 107–296), the Administration for
Children and Families (ACF), Office of
Refugee Resettlement (ORR), is charged
with the care and placement of
Average
burden hours
per response
8
8
0.5
0.25
Total burden
hours
216
108
unaccompanied alien children in
Federal custody, and implementing a
policy for the release of these children,
when appropriate, upon the request of
suitable sponsors while awaiting
immigration proceedings. In order for
ORR to make determinations regarding
the release of these children, the
potential sponsors must meet certain
conditions pursuant to section 462 of
the Homeland Security Act and the
Flores v. Reno Settlement Agreement
No. CV85 4544–RJK (C.D. Cal. 1997).
The proposed information collection
requests information to be utilized by
ORR for determining the suitability of a
sponsor/respondent for the release of a
minor from ORR custody. The proposed
instruments are the Sponsor’s
Agreement to Conditions of Release,
Verification of Release, Family
Reunification Packet, and the
Authorization for Release of
Information.
Respondents: Sponsors requesting
release of unaccompanied alien children
to their custody.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
rfrederick on PROD1PC67 with NOTICES
Sponsor’s Agreement to Conditions of Release ...........................................
Verification of Release ...................................................................................
Family Reunification Packet ..........................................................................
Authorization for Release of Information .......................................................
Estimated Total Annual Burden
Hours: 6,071.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
VerDate Aug<31>2005
15:16 May 02, 2008
Jkt 214001
4,288
4,288
4,288
4,288
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
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
Number of
responses
per
respondent
Average burden
hours per
response
2
1
18
15
.0835
.167
.0416
.0222
Total burden
hours
716
716
3,211
1,428
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
E:\FR\FM\05MYN1.SGM
05MYN1
Federal Register / Vol. 73, No. 87 / Monday, May 5, 2008 / Notices
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: April 28, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E8–9762 Filed 5–2–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0257]
Draft Prescription Drug User Fee Act IV
Drug Safety Five-Year Plan; Availability
for Comment
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability for public comment of the
draft drug safety 5-year plan entitled
‘‘Prescription Drug User Fee Act
(PDUFA) IV Drug Safety Five-Year
Plan.’’ This plan is intended to
communicate FDA’s strategy for meeting
the commitments for enhancing and
modernizing the drug safety system
within the context of the PDUFA IV
program.
DATES: Submit written or electronic
comments on the draft drug safety 5year plan by June 19, 2008.
ADDRESSES: Submit written requests for
single copies of the draft plan to the
Office of Executive Programs, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 6100,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist that office in processing your
requests. Submit written comments on
the draft drug safety 5-year plan to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852. Submit electronic comments
to https://www.regulations.gov. See the
SUPPLEMENTARY INFORMATION section for
electronic access to the document.
FOR FURTHER INFORMATION CONTACT:
Jayne C. Ware, Food and Drug
rfrederick on PROD1PC67 with NOTICES
SUMMARY:
VerDate Aug<31>2005
15:16 May 02, 2008
Jkt 214001
Administration, Center for Drug
Evaluation and Research, Office of
Executive Programs, 10903 New
Hampshire Ave., Bldg. 51, rm. 6100,
Silver Spring, MD 20993–0002, 301–
796–3200.
SUPPLEMENTARY INFORMATION:
I. Background
On September 27, 2007, President
Bush signed into law the Food and Drug
Administration Amendments Act of
2007, which includes the
reauthorization and expansion of
PDUFA. The reauthorization of PDUFA
will significantly broaden and
modernize the agency’s drug safety
program and facilitate more efficient
development of safe and effective new
medications for the American public.
During the user fee negotiation process
leading up to the renewal of PDUFA,
FDA and the relevant regulated
industries mutually agreed to certain
commitments that the FDA will carry
out during fiscal years 2008 through
2012. Congress signaled its agreement
with the commitments by authorizing
PDUFA funds for them. Among those
commitments is the responsibility of the
FDA to develop and periodically update
a 5-year plan describing activities that
will lead to enhancing and modernizing
FDA’s drug safety system.
FDA is announcing for public
comment the availability of the draft
drug safety 5-year plan entitled
‘‘Prescription Drug User Fee Act
(PDUFA) IV Drug Safety Five-Year
Plan.’’ This plan is intended to
communicate FDA’s strategy for meeting
the commitments for enhancing and
modernizing the drug safety system
within the context of the PDUFA IV
program. The plan describes the
agency’s strategy for achieving the
commitments defined in section VIII,
Enhancement and Modernization of the
FDA Drug Safety System, and section
IX, Review of Proprietary Names to
Reduce Medication Errors, of the
PDUFA IV Performance Goals (https://
www.fda.gov/oc/pdufa4/
pdufa4goals.html). At the end of the
comment period, FDA will review the
comments, update the ‘‘PDUFA IV Drug
Safety Five-Year Plan,’’ and publish the
final version.
II. Comments
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
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
24599
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.
Please note that on January 15, 2008,
the FDA Division of Dockets
Management Web site transitioned to
the Federal Dockets Management
System (FDMS). FDMS is a
Government-wide, electronic docket
management system. Electronic
comments or submissions will be
accepted by FDA only through FDMS at
https://www.regulations.gov.
III. Electronic Access
Persons with access to the Internet
may obtain the document at https://
www.fda.gov/cder/pdufa/
PDUFA_IV_5yr_plan_draft.pdf.
Dated: April 25, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and
Planning.
[FR Doc. E8–9726 Filed 5–2–08; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
The 11th Annual Food and Drug
Administration-Orange County
Regulatory Affairs Educational
Conference
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of meeting.
The Food and Drug Administration
(FDA) is announcing the following
conference: 11th Annual Educational
Conference co-sponsored with the
Orange County Regulatory Affairs
Discussion Group (OCRA). The
conference is intended to provide the
Drug, Device, and Biologics industries
with an opportunity to interact with
FDA reviewers and compliance officers
from the Centers and District Offices, as
well as other industry experts. The main
focus of this interactive conference will
be product approval, compliance, and
risk management in the three medical
product areas. Industry speakers,
interactive questions and answers, and
workshop sessions will also be included
to assure open exchange and dialogue
on the relevant regulatory issues.
Date and Time: The conference will
be held on June 11 and 12, 2008, from
7:30 a.m. to 5 p.m.
Location: The conference will be held
at the Irvine Marriott Hotel, 18000 Von
Karman Ave., Irvine, CA 92612.
E:\FR\FM\05MYN1.SGM
05MYN1
]]>Agencies
[Federal Register Volume 73, Number 87 (Monday, May 5, 2008)]
[Notices]
[Pages 24598-24599]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-9762]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Reunification Procedures for Unaccompanied Alien Children.
OMB No.: 0970-0278.
Description: Following the passage of the 2002 Homeland Security
Act (Pub. L. 107-296), the Administration for Children and Families
(ACF), Office of Refugee Resettlement (ORR), is charged with the care
and placement of unaccompanied alien children in Federal custody, and
implementing a policy for the release of these children, when
appropriate, upon the request of suitable sponsors while awaiting
immigration proceedings. In order for ORR to make determinations
regarding the release of these children, the potential sponsors must
meet certain conditions pursuant to section 462 of the Homeland
Security Act and the Flores v. Reno Settlement Agreement No. CV85 4544-
RJK (C.D. Cal. 1997).
The proposed information collection requests information to be
utilized by ORR for determining the suitability of a sponsor/respondent
for the release of a minor from ORR custody. The proposed instruments
are the Sponsor's Agreement to Conditions of Release, Verification of
Release, Family Reunification Packet, and the Authorization for Release
of Information.
Respondents: Sponsors requesting release of unaccompanied alien
children to their custody.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Sponsor's Agreement to Conditions of Release.... 4,288 2 .0835 716
Verification of Release......................... 4,288 1 .167 716
Family Reunification Packet..................... 4,288 18 .0416 3,211
Authorization for Release of Information........ 4,288 15 .0222 1,428
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 6,071.
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
[[Page 24599]]
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: April 28, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E8-9762 Filed 5-2-08; 8:45 am]
BILLING CODE 4184-01-M
