Renewal of Charters for Certain Federal Advisory Committees, 6090-6091 [2015-02097]
Download as PDF
6090
Federal Register / Vol. 80, No. 23 / Wednesday, February 4, 2015 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–0990–0382–
60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Assistant
Secretary for Health, Office of
Adolescent Health, HHS.
ACTION: Notice.
AGENCY:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to request an extension without change
of a currently approved Information
Collection Request (ICR) to the Office of
Management and Budget (OMB). Prior
to submitting that request to OMB, OS
seeks comments from the public
SUMMARY:
regarding the burden estimate, below, or
any other aspect of the ICR.
DATES: Comments on the ICR must be
received on or before April 6, 2015.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
document identifier HHS–OS–0990–
0382–Extension–60D for reference.
Information Collection Request Title:
Evaluation of Pregnancy Prevention
Approaches—First Follow-up
Abstract: The Office of Adolescent
Health (OAH), U.S. Department of
Health and Human Services (HHS) is
requesting an extension without change
of a currently approved information
collection request by OMB. The purpose
of the extension is to complete the
ongoing follow-up data collection for
the Evaluation of Adolescent Pregnancy
Prevention Approaches (PPA), a multisite random assignment evaluation of
promising approaches to teen pregnancy
prevention.
Need and Proposed Use of the
Information: The PPA study is being
conducted in seven program sites
around the country. The proposed
extension is necessary to complete
ongoing follow-up data collection in
five of the seven study sites. The
resulting data will be used in a rigorous
program impact analysis to assess the
effectiveness of each program in
reducing rates of teen pregnancy and
associated sexual risk behaviors.
Likely Respondents: The 1484 youth
participants who agreed to participate in
the study upon sample enrollment in 5
impact study sites.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Oklahoma Institute for Child Advocacy (OICA) ...............................................
Ohio Health ......................................................................................................
Children’s Hospital Los Angeles ......................................................................
EngenderHealth ...............................................................................................
Princeton Center for Leadership Training .......................................................
Total ..........................................................................................................
294
148
254
240
548
........................
2
3
2
2
2
........................
42/60
42/60
36/60
36/60
36/60
........................
OS specifically requests comments on
(1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Darius Taylor,
Information Collection Clearance Officer.
[FR Doc. 2015–02144 Filed 2–3–15; 8:45 am]
mstockstill on DSK4VPTVN1PROD with NOTICES
BILLING CODE 4168–11–P
VerDate Sep<11>2014
18:18 Feb 03, 2015
Jkt 235001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Renewal of Charters for Certain
Federal Advisory Committees
Office of the Secretary,
Department of Health and Human
Services.
ACTION: Notice.
AGENCY:
As stipulated by the Federal
Advisory Committee Act, as amended (5
U.S.C. App), the U.S. Department of
Health and Human Services is hereby
announcing that the charters have been
renewed for the following federal
advisory committees for which the
National Institutes of Health provides
management support: National
Toxicology Program Board of Scientific
Counselors (NTPBSC) and National
Toxicology Program Special Emphasis
Panel (NTPSEP). Functioning as federal
advisory committees, these committees
are governed by the provisions of the
SUMMARY:
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
Total burden
hours
412
310
305
288
658
1,973
Federal Advisory Committee Act
(FACA). Under FACA, the charter for a
federal advisory committee must be
renewed every two years in order for the
committee to continue to operate.
FOR FURTHER INFORMATION CONTACT:
Jennifer Spaeth, Director, Office of
Federal Advisory Committee Policy,
Office of the Director, National
Institutes of Health, 6701 Democracy
Boulevard, Suite 1000, Bethesda,
Maryland 20892 (Mail code 4875).
Telephone (301) 496–2123, or
spaethj@od.nih.gov.
SUPPLEMENTARY INFORMATION: In 1978
the Secretary of Health and Human
Services established the National
Toxicology Program (NTP) to coordinate
toxicological testing programs within
the Department, strengthen the science
base in toxicology, develop and validate
improved testing methods, and provide
information about potentially toxic
agents to health regulatory and research
agencies, medical and scientific
communities, and the public. The NTP
is an interagency program that provides
E:\FR\FM\04FEN1.SGM
04FEN1
Federal Register / Vol. 80, No. 23 / Wednesday, February 4, 2015 / Notices
information that improves the nation’s
ability to evaluate potential human
health effects from chemical or physical
exposures. The NTP plays a critical role
in providing needed scientific data,
interpretations, and guidance on the
appropriate uses of data to regulatory
agencies and other groups involved in
health-related research and in providing
information to regulatory agencies about
alternative methods for toxicity
screening.
The results of NTP’s long-term,
generally two-year, toxicology and
carcinogenicity studies, are published as
NTP Technical Reports. The NTP uses
established criteria to evaluate the
findings and determine the strength of
the evidence for conclusions regarding
the carcinogenic activity of each
substance evaluated. Panels are
technical, scientific advisory bodies
established to provide independent
scientific peer review of the draft NTP
Technical Reports.
Copies of the charters for the
designated committees can be obtained
by accessing the FACA data base that is
maintained by the Committee
Management Secretariat under the
General Services Administration.
Dated: January 29, 2015.
Carolyn A. Baum,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–02097 Filed 2–3–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
6091
OMB No.: 0970–0423.
Description: The Office of Head Start
is proposing to renew without changes
authority to collect information
pursuant to 45 CFR part 1301. These
provisions are applicable to program
administration and grants
administration under the Head Start
Act, as amended. The provisions specify
the requirements for grantee agencies for
insurance and bonding, the submission
of audits, matching of federal funds,
accounting systems certifications and
other provisions applicable to personnel
management.
Respondents: Head Start and Early
Head Start program grant recipients.
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: 45 CFR 1301 Head Start Grant
Administration.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Information Collection ......................................................................................
mstockstill on DSK4VPTVN1PROD with NOTICES
Instrument
2,700
1
2
5,400
Estimated Total Annual Burden
Hours: 5,400.
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 Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email 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
VerDate Sep<11>2014
18:18 Feb 03, 2015
Jkt 235001
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2015–02139 Filed 2–3–15; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
National Vaccine Injury Compensation
Program; List of Petitions Received
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
The Health Resources and
Services Administration (HRSA) is
publishing this notice of petitions
received under the National Vaccine
Injury Compensation Program (the
SUMMARY:
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
Program), as required by Section
2112(b)(2) of the Public Health Service
(PHS) Act, as amended. While the
Secretary of Health and Human Services
is named as the respondent in all
proceedings brought by the filing of
petitions for compensation under the
Program, the United States Court of
Federal Claims is charged by statute
with responsibility for considering and
acting upon the petitions.
FOR FURTHER INFORMATION CONTACT: For
information about requirements for
filing petitions, and the Program in
general, contact the Clerk, United States
Court of Federal Claims, 717 Madison
Place NW., Washington, DC 20005,
(202) 357–6400. For information on
HRSA’s role in the Program, contact the
Director, National Vaccine Injury
Compensation Program, 5600 Fishers
Lane, Room 11C–26, Rockville, MD
20857; (301) 443–6593.
SUPPLEMENTARY INFORMATION: The
Program provides a system of no-fault
compensation for certain individuals
who have been injured by specified
childhood vaccines. Subtitle 2 of Title
XXI of the PHS Act, 42 U.S.C. 300aa–
10 et seq., provides that those seeking
compensation are to file a petition with
the U.S. Court of Federal Claims and to
serve a copy of the petition on the
E:\FR\FM\04FEN1.SGM
04FEN1
Agencies
[Federal Register Volume 80, Number 23 (Wednesday, February 4, 2015)]
[Notices]
[Pages 6090-6091]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-02097]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Renewal of Charters for Certain Federal Advisory Committees
AGENCY: Office of the Secretary, Department of Health and Human
Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: As stipulated by the Federal Advisory Committee Act, as
amended (5 U.S.C. App), the U.S. Department of Health and Human
Services is hereby announcing that the charters have been renewed for
the following federal advisory committees for which the National
Institutes of Health provides management support: National Toxicology
Program Board of Scientific Counselors (NTPBSC) and National Toxicology
Program Special Emphasis Panel (NTPSEP). Functioning as federal
advisory committees, these committees are governed by the provisions of
the Federal Advisory Committee Act (FACA). Under FACA, the charter for
a federal advisory committee must be renewed every two years in order
for the committee to continue to operate.
FOR FURTHER INFORMATION CONTACT: Jennifer Spaeth, Director, Office of
Federal Advisory Committee Policy, Office of the Director, National
Institutes of Health, 6701 Democracy Boulevard, Suite 1000, Bethesda,
Maryland 20892 (Mail code 4875). Telephone (301) 496-2123, or
spaethj@od.nih.gov.
SUPPLEMENTARY INFORMATION: In 1978 the Secretary of Health and Human
Services established the National Toxicology Program (NTP) to
coordinate toxicological testing programs within the Department,
strengthen the science base in toxicology, develop and validate
improved testing methods, and provide information about potentially
toxic agents to health regulatory and research agencies, medical and
scientific communities, and the public. The NTP is an interagency
program that provides
[[Page 6091]]
information that improves the nation's ability to evaluate potential
human health effects from chemical or physical exposures. The NTP plays
a critical role in providing needed scientific data, interpretations,
and guidance on the appropriate uses of data to regulatory agencies and
other groups involved in health-related research and in providing
information to regulatory agencies about alternative methods for
toxicity screening.
The results of NTP's long-term, generally two-year, toxicology and
carcinogenicity studies, are published as NTP Technical Reports. The
NTP uses established criteria to evaluate the findings and determine
the strength of the evidence for conclusions regarding the carcinogenic
activity of each substance evaluated. Panels are technical, scientific
advisory bodies established to provide independent scientific peer
review of the draft NTP Technical Reports.
Copies of the charters for the designated committees can be
obtained by accessing the FACA data base that is maintained by the
Committee Management Secretariat under the General Services
Administration.
Dated: January 29, 2015.
Carolyn A. Baum,
Program Analyst, Office of Federal Advisory Committee Policy.
[FR Doc. 2015-02097 Filed 2-3-15; 8:45 am]
BILLING CODE 4140-01-P