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]


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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
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