Proposed Information Collection Activity; Comment Request, 15758-15759 [E8-5951]
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15758
Federal Register / Vol. 73, No. 58 / Tuesday, March 25, 2008 / Notices
recommendations on the use of the two
in vitro NRU test methods, as well as
recommended test method protocols,
recommendations for future studies to
further characterize the usefulness and
limitations of in vitro methods for
assessing acute systemic toxicity,
recommended performance standards
for tests with similar scientific
principles and that measure or predict
acute oral systemic toxicity, the peer
panel report and Federal Register
notices. The final BRD, which provides
the supporting documentation for this
report, is available as a separate
document. The ICCVAM Test Method
Evaluation Report and the supporting
final BRD were forwarded to U.S.
Federal agencies for their consideration
for regulatory acceptance as required by
the ICCVAM Authorization Act of 2000
(42 U.S.C. 285l–3). Agencies’ responses
to the test method recommendations
will be posted on the ICCVAM/
NICEATM Web site as they are received.
Background Information on ICCVAM,
NICEATM, and SACATM
ICCVAM is an interagency committee
composed of representatives from 15
Federal regulatory and research agencies
that use, generate, or disseminate
toxicological information. ICCVAM
conducts technical evaluations of new,
revised, and alternative methods with
regulatory applicability and promotes
the scientific validation and regulatory
acceptance of toxicological test methods
that more accurately assess the safety
and hazards of chemicals and products
and that refine, reduce, and replace
animal use. The ICCVAM Authorization
Act of 2000 established ICCVAM as a
permanent interagency committee of the
NIEHS under NICEATM. NICEATM
administers ICCVAM and provides
scientific and operational support for
ICCVAM-related activities. NICEATM
and ICCVAM work collaboratively to
evaluate new and improved test
methods applicable to the needs of U.S.
Federal agencies. Additional
information about ICCVAM and
NICEATM can be found on their Web
site (https://iccvam.niehs.nih.gov).
SACATM was established January 9,
2002, and is composed of scientists from
the public and private sectors (Federal
Register, Vol. 67, No. 49, page 11358).
SACATM provides advice to the
Director of the NIEHS, to ICCVAM, and
to NICEATM regarding the statutorily
mandated duties of ICCVAM and
activities of NICEATM. Additional
information about SACATM, including
the charter, roster, and records of past
meetings, can be found at https://
ntp.niehs.nih.gov/ see ‘‘Advisory Board
& Committees’’ (or directly at https://
ntp.niehs.nih.gov/go/167).
Dated: March 14, 2008.
Samuel H. Wilson,
Acting Director, National Institute of
Environmental Health Sciences and National
Toxicology Program.
[FR Doc. E8–5936 Filed 3–24–08; 8:45 am]
FOR FURTHER INFORMATION CONTACT:
https://www.hhs.gov/healthit/ahic/
confidentiality/.
SUPPLEMENTARY INFORMATION: The
Workgroup Members will continue
discussing and evaluating the
confidentiality, privacy, and security
protections and requirements for
participants in electronic health
information exchange environments.
The meeting will be available via Web
cast. For additional information, go to:
https://www.hhs.gov/healthit/ahic/
cps_instruct.html.
Dated: March 13, 2008.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. E8–5853 Filed 3–24–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology;
American Health Information
Community Confidentiality, Privacy, &
Security Workgroup Meeting
ACTION:
Announcement of meeting.
SUMMARY: This notice announces the
18th meeting of the American Health
Information Community Confidentiality,
Privacy, & Security Workgroup in
accordance with the Federal Advisory
Committee Act (Pub. L. No. 92–463, 5
U.S.C., App.)
DATES: April 17, 2008, from 1 p.m. to 5
p.m. (Eastern Time).
ADDRESSES: Mary C. Switzer Building
(330 C Street, SW., Washington, DC
20201), Conference Room 4090 (please
bring photo ID for entry to a Federal
building).
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Grants to States for Access and
Visitation: State Child Access Program
Survey.
OMB No.: 0970–0204.
Description: On an annual basis,
States must provide OCSE with data on
programs that the Grants to States for
Access and Visitation Program has
funded. These program reporting
requirements include, but are not
limited to, the collection of data on the
number of parents served, types of
services delivered, program outcomes,
client socio-economic data, referral
sources, and other relevant data. OCSE
is proposing revisions to the current
survey.
ANNUAL BURDEN ESTIMATES
No. of respondents
No. of responses per
respondent
Average burden hours per
response
Total burden
hours
State Child Access Program Survey ................................................................
mstockstill on PROD1PC66 with NOTICES
Instrument
314
1
15
4,710
Estimated Total Annual Burden
Hours: 4,710.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
VerDate Aug<31>2005
18:33 Mar 24, 2008
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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
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: Office of
Administration, Office of Information
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15759
Federal Register / Vol. 73, No. 58 / Tuesday, March 25, 2008 / Notices
Services, 370 L’Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACE
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
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: March 19, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E8–5951 Filed 3–24–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Temporary Assistance for Needy
Families (TANF) State Plan; Guidance.
OMB No.: 0970–0145.
Description: The State plan is a
mandatory statement submitted to the
Secretary of the Department of Health
and Human Services by the State. It
consists of an outline of how the State’s
TANF program will be administered
and operated and certain required
certifications by the State’s Chief
Executive Officer. Its submittal triggers
the State’s family assistance grant
funding and it is used to provide the
public with information about the
program. If a State makes changes in its
program, it must submit a State plan
amendment.
Respondents: The 50 States, the
District of Columbia, Guam, Puerto Rico
and the Virgin Islands.
ANNUAL BURDEN ESTIMATES
No. of
respondents
Instrument
mstockstill on PROD1PC66 with NOTICES
Temporary Assistance for Needy Families (TANF) State Plan Guidance ......
Estimated Total Annual Burden
Hours: 891.
In compliance with the requirements
of Section 506(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
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.
VerDate Aug<31>2005
18:33 Mar 24, 2008
Jkt 214001
54
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Dated: March 19, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E8–5952 Filed 3–24–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–D–0149] (formerly
Docket No. 2007D–0031)
Global Harmonization Task Force,
Study Group 4; Final Document;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a final document that has
been prepared by Study Group 4 of the
Global Harmonization Task Force
(GHTF). This document represents a
harmonized proposal and
recommendation from Study Group 4 of
the GHTF that may be used by
governments developing and updating
their regulatory requirements for
medical devices. This document is
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No. of
responses per
respondent
0.5
Average
burden hours
per response
33
Total burden
hours
891
intended to provide information only
and does not describe current regulatory
requirements; elements of this
document may not be consistent with
current U.S. regulatory requirements.
DATES: Submit written or electronic
comments on this guidance at any time.
General comments on agency guidance
documents are welcome at any time.
ADDRESSES: Submit written requests for
single copies of the guidance document
to the Division of Small Manufacturers,
International, and Consumer Assistance
(HFZ–220), Center for Devices and
Radiological Health, Food and Drug
Administration, 1350 Piccard Dr.,
Rockville, MD 20850. Send one selfaddressed adhesive label to assist that
office in processing your request, or fax
your request to 240–276–3151. See the
SUPPLEMENTARY INFORMATION section for
information on electronic access to the
guidance. Submit written comments
concerning this document 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. Identify
comments with the docket number
found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: Jan
Welch, GHTF, Study Group 4, Office of
Compliance, Center for Devices and
Radiological Health (HFZ–320), Food
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[Federal Register Volume 73, Number 58 (Tuesday, March 25, 2008)]
[Notices]
[Pages 15758-15759]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-5951]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Grants to States for Access and Visitation: State Child
Access Program Survey.
OMB No.: 0970-0204.
Description: On an annual basis, States must provide OCSE with data
on programs that the Grants to States for Access and Visitation Program
has funded. These program reporting requirements include, but are not
limited to, the collection of data on the number of parents served,
types of services delivered, program outcomes, client socio-economic
data, referral sources, and other relevant data. OCSE is proposing
revisions to the current survey.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
No. of Average burden
Instrument No. of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
State Child Access Program Survey........... 314 1 15 4,710
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 4,710.
In compliance with the requirements of Section 506(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: Office of Administration, Office of
Information
[[Page 15759]]
Services, 370 L'Enfant Promenade, SW., Washington, DC 20447, Attn: ACE
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
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: March 19, 2008.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E8-5951 Filed 3-24-08; 8:45 am]
BILLING CODE 4184-01-M