Notice of Award of Non-Competitive Grant, 50373 [E7-17216]

Download as PDF Federal Register / Vol. 72, No. 169 / Friday, August 31, 2007 / Notices beneficiaries on a mandatory basis into managed care entities without section 1115 or 1915(b) waiver authority; Frequency: On occasion; Affected Public: State, local, or tribal government; Number of Respondents: 56; Total Annual Responses: 10; Total Annual Hours: 100. To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web Site address at http://www.cms.hhs.gov/ PaperworkReductionActof1995, or email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call the Reports Clearance Office on (410) 786– 1326. To be assured consideration, comments and recommendations for the proposed information collections must be received at the address below, no later than 5 p.m. on October 30, 2007. CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development—A, Attention: Melissa Musotto, Room C4–26–05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. conducting of adolescent pregnancy approaches. They are the only research group currently conducting a study of size and scope that provides for access to schools and study participants for the collection of additional data needed. Building on the existing study already underway saves the cost of initiating a study from the ground up. FOR FURTHER INFORMATION CONTACT: Stan Koutstaal, Ph.D., Director, Division of Abstinence Education, Family and Youth Services Bureau, ACYF, ACF, DHHS. Portals Building, Suite 800, 1250 Maryland Avenue, SW., Washington, DC 20024; 202–401–6959. Dated: August 24, 2007. Michelle Shortt, Director, Regulations Development Group, Office of Strategic Operations and Regulatory Affairs. [FR Doc. E7–17351 Filed 8–30–07; 8:45 am] Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Devices: Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use BILLING CODE 4120–01–P Administration on Children, Youth, and Families (ACYF), ACF, DHHS. ACTION: Notice. AGENCY: sroberts on PROD1PC70 with NOTICES Food and Drug Administration [Docket No. 2007N–0325] ACTION: Notice of Award of Non-Competitive Grant CFDA No.: 93.010, Community-Based Abstinence Education. Legislative Authority: Title XI, Section 1110 of the Social Security Act. Amount of Award: $2,500,000. Project Period: September 30, 2007– March 30, 2009 (18 months). Justification for the Exception to Competition: ACYF will award service grant funds without competition to the Prevention Research Center at the University of Texas Health Science Center at Houston to build on a longitudinal study they are currently Jkt 211001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration, HHS. Administration for Children and Families 00:43 Aug 31, 2007 BILLING CODE 4184–01–P AGENCY: DEPARTMENT OF HEALTH AND HUMAN SERVICES VerDate Aug<31>2005 Dated: August 24, 2007. Joan E. Ohl, Commissioner, Administration on Children, Youth and Families. [FR Doc. E7–17216 Filed 8–30–07; 8:45 am] 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 information collection, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the reporting requirements for the collection ‘‘Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use.’’ DATES: Submit written or electronic comments on the collection of information by October 30, 2007. PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 50373 Submit electronic comments on the collection of information to: http://www.fda.gov/ dockets/ecomments or 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. 1061, Rockville, MD 20852. All comments should be identified with the docket number found in brackets in the heading of this document. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of Chief Information Officer (HFA–250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827– 1472. 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. SUPPLEMENTARY INFORMATION: 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. E:\FR\FM\31AUN1.SGM 31AUN1

Agencies

[Federal Register Volume 72, Number 169 (Friday, August 31, 2007)]
[Notices]
[Page 50373]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-17216]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Notice of Award of Non-Competitive Grant

AGENCY: Administration on Children, Youth, and Families (ACYF), ACF, 
DHHS.

ACTION: Notice.

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    CFDA No.: 93.010, Community-Based Abstinence Education.
    Legislative Authority: Title XI, Section 1110 of the Social 
Security Act.
    Amount of Award: $2,500,000.
    Project Period: September 30, 2007-March 30, 2009 (18 months).
    Justification for the Exception to Competition: ACYF will award 
service grant funds without competition to the Prevention Research 
Center at the University of Texas Health Science Center at Houston to 
build on a longitudinal study they are currently conducting of 
adolescent pregnancy approaches. They are the only research group 
currently conducting a study of size and scope that provides for access 
to schools and study participants for the collection of additional data 
needed. Building on the existing study already underway saves the cost 
of initiating a study from the ground up.

FOR FURTHER INFORMATION CONTACT: Stan Koutstaal, Ph.D., Director, 
Division of Abstinence Education, Family and Youth Services Bureau, 
ACYF, ACF, DHHS. Portals Building, Suite 800, 1250 Maryland Avenue, 
SW., Washington, DC 20024; 202-401-6959.

    Dated: August 24, 2007.
Joan E. Ohl,
Commissioner, Administration on Children, Youth and Families.
[FR Doc. E7-17216 Filed 8-30-07; 8:45 am]
BILLING CODE 4184-01-P