Submission for OMB Review; Comment Request, 43988-43989 [2010-18343]

Download as PDF 43988 Federal Register / Vol. 75, No. 143 / Tuesday, July 27, 2010 / Notices Dated: July 20, 2010. Maryam I. Daneshvar, Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–18288 Filed 7–26–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–10–09BC] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project Exploring HIV Prevention Communication Among Black Men Who Have Sex With Men in New York City: Project BROTHA—New. National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC is requesting OMB approval to administer a survey, conduct interviews and offer HIV rapid testing in black men who have sex with men (BMSM) and other men who have sex with men (MSM) in New York City. The purpose of the proposed study is to assess how interpersonal communication within BMSM social networks may be related to risk for HIV infection and attitudes towards HIV testing. After screening for eligibility, a total of 300 BMSM and other MSM in their social networks will be enrolled in 2 phases: (1) 350 BMSM will be recruited and screened to find 100 eligible BMSM participants, and (2) the 100 first phase participants will then recruit 200 other MSM within their social networks to participate in the second phase. Quantitative surveys will be administered by computers and personal interviews will be conducted to collect qualitative data (at baseline and 3-month follow-up). Participants in both phases will be offered rapid HIV testing, and declining an HIV test will not negatively impact their study participation. The research questions being explored are relevant for understanding how interpersonal communication with members of one’s social networks are related to risk for contracting HIV infection and attitudes towards HIV testing. This study will provide important epidemiologic information useful for the development of HIV prevention interventions for BMSM. Men will complete a 5-minute eligibility screening interview. The baseline computer-based survey will take 45 minutes. The qualitative interview will take approximately 75 minutes. The number of respondents who will accept HIV testing is estimated to be 200 (accounting for those who did not test at baseline and those who do not consent to test at follow-up). HIV counseling and rapid testing will take 45 minutes. The 3-month follow-up survey will take approximately 30 minutes; the follow-up qualitative interview will take approximately 45 minutes. There is no cost to the respondents other than their time. The estimated annualized burden hours are 1338. ESTIMATE OF ANNUALIZED BURDEN HOURS Types of data collection BMSM/MSM volunteers ...... Screening ....................................................................... A–CASI Baseline ............................................................ Interview Baseline .......................................................... HIV Testing & Counseling Baseline ............................... A–CASI 3 month Follow-up ............................................ Interview 3 month Follow-up .......................................... HIV Testing & Counseling 3 month Follow-up ............... Dated: July 21, 2010. Maryam I. Daneshvar Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–18396 Filed 7–26–10; 8:45 am] BILLING CODE 4163–18–P sroberts on DSKD5P82C1PROD with NOTICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: ADP & Services Conditions for FFP for ACF. VerDate Mar<15>2010 16:30 Jul 26, 2010 Jkt 220001 OMB No.: 0992–0005. Description: The Advance Planning Document (APD) process, established in the rules at 45 CFR Part 95, Subpart F, is the procedure by which States request and obtain approval for Federal financial participation in their cost of acquiring Automatic Data Processing (ADP) equipment and services. State agencies that submit APD requests provide the Department of Health and Human Services (HHS) with the following information necessary to determine the States’ needs to acquire the requested ADP equipment and/or services: (1) A statement of need; PO 00000 Frm 00074 Fmt 4703 Number of responses per respondent Number of respondents Respondents Sfmt 4703 750 300 300 200 300 300 200 Burden per response (in hours) 1 1 1 1 1 1 1 5/60 45/60 1.25 45/60 30/60 45/60 45/60 (2) A requirements analysis and feasibility study; (3) A cost benefit analysis; (4) A proposed activity schedule; and, (5) A proposed budget. HHS’ determination of a State Agency’s need to acquire requested ADP equipment or services is authorized at sections 402(a)(5), 452(a)(1), 1902(a)(4) and 1102 of the Social Security Act. Respondents: States. E:\FR\FM\27JYN1.SGM 27JYN1 Federal Register / Vol. 75, No. 143 / Tuesday, July 27, 2010 / Notices 43989 ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response RFP and Contract ............................................................................................ Emergency Funding Request .......................................................................... Service Agreements ........................................................................................ Biennial Reports .............................................................................................. Advance Planning Document .......................................................................... Estimated Total Annual Burden Hours: ........................................................... 50 27 14 50 50 ........................ 1.54 1 1 1 1.84 ........................ 1.50 1 1 1.50 60 ........................ Additional Information Dated: July 22, 2010. Robert Sargis, Reports Clearance Officer. 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 and to allow 60 days for public comment in response to the notice. This notice solicits comments on the sample collection plan for dogs treated with the drug SLENTROL. DATES: Submit either electronic or written comments on the collection of information by September 27, 2010. ADDRESSES: Submit electronic comments on the collection of information to https:// 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. FOR FURTHER INFORMATION CONTACT: Denver Presley Jr., Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–396– 3793. [FR Doc. 2010–18343 Filed 7–26–10; 8:45 am] SUPPLEMENTARY INFORMATION: SUMMARY: 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: 202–395–7285, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the Administration for Children and Families. BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration sroberts on DSKD5P82C1PROD with NOTICES [Docket No. FDA–2010–N–0358] Agency Information Collection Activities; Proposed Collection; Comment Request; Sample Collection Plan for Dogs Treated With SLENTROL AGENCY: Food and Drug Administration, HHS. ACTION: Notice. VerDate Mar<15>2010 17:49 Jul 26, 2010 Jkt 220001 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 before submitting the collection to OMB for approval. To comply with this PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 Total burden hours 115.50 27 14 75 5,520 5,751.50 requirement, FDA is publishing notice of the proposed collection of information set forth in this document. 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. Sample Collection Plan for Dogs Treated With SLENTROL—21 CFR 514.80 (OMB Control Number 0910– NEW) FDA’s Center for Veterinary Medicine (CVM) is planning a pharmacogenomic study to examine whether adverse drug events (ADEs) experienced with SLENTROL, an anti-obesity drug approved for dogs, are associated with genetic variations in the dogs treated. Pharmacogenomics involves the use of genome-wide analyses to identify genes with altered expression or activation as a result exposure to a drug. Preliminary analysis by CVM has indicated potential correlations between dog breeds and some ADEs. The study would collect a blood sample and buccal swab from animals that have been treated with SLENTROL and experienced specific ADEs (i.e., reactors), and animals that have been treated with SLENTROL and that have not experienced ADEs (i.e., controls). The samples would be analyzed by FDA using microarray analysis and single nucleotide polymorphism analysis to determine possible genetic variations associated with the ADEs reported. If this project identifies definite genotype mutations E:\FR\FM\27JYN1.SGM 27JYN1

Agencies

[Federal Register Volume 75, Number 143 (Tuesday, July 27, 2010)]
[Notices]
[Pages 43988-43989]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-18343]

-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

Submission for OMB Review; Comment Request

Title: ADP & Services Conditions for FFP for ACF.
OMB No.: 0992-0005.
Description: The Advance Planning Document (APD) process,
established in the rules at 45 CFR Part 95, Subpart F, is the procedure
by which States request and obtain approval for Federal financial
participation in their cost of acquiring Automatic Data Processing
(ADP) equipment and services. State agencies that submit APD requests
provide the Department of Health and Human Services (HHS) with the
following information necessary to determine the States' needs to
acquire the requested ADP equipment and/or services:
(1) A statement of need;
(2) A requirements analysis and feasibility study;
(3) A cost benefit analysis;
(4) A proposed activity schedule; and,
(5) A proposed budget.
HHS' determination of a State Agency's need to acquire requested
ADP equipment or services is authorized at sections 402(a)(5),
452(a)(1), 1902(a)(4) and 1102 of the Social Security Act.
Respondents: States.

[[Page 43989]]

Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
RFP and Contract................................ 50 1.54 1.50 115.50
Emergency Funding Request....................... 27 1 1 27
Service Agreements.............................. 14 1 1 14
Biennial Reports................................ 50 1 1.50 75
Advance Planning Document....................... 50 1.84 60 5,520
Estimated Total Annual Burden Hours:............ .............. .............. .............. 5,751.50
----------------------------------------------------------------------------------------------------------------

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-
395-7285, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for
the Administration for Children and Families.

Dated: July 22, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-18343 Filed 7-26-10; 8:45 am]
BILLING CODE 4184-01-P

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