Submission for OMB Review; Comment Request, 67820 [2012-27583]

Download as PDF 67820 Federal Register / Vol. 77, No. 220 / Wednesday, November 14, 2012 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: 45 CFR 1303 Appeal Procedures for Head Start Grantees and Current or Prospective Delegate Agencies. OMB No.: 0980–0242. Description: Section 646 of the Head Start Act requires the Secretary to prescribe a timeline for conducting administrative hearings when adverse actions are taken or proposed against Head Start or Early Head Start grantees or delegate agencies. The Office of Head Start is proposing to renew without changes this rule which implements these requirements and which prescribe when a grantee must submit information and what that information should include to support a contention that adverse action should not be taken. Respondents: Head Start and Early Head Start grantees and delegate agencies against which the Head Start Bureau has taken or proposes to take adverse actions. ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours Appeal .............................................................................................................. 20 1 26 520 Estimated Total Annual Burden Hours: 520 DEPARTMENT OF HEALTH AND HUMAN SERVICES Additional Information Food and Drug Administration Copies of the proposed collection may be obtained 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. All requests should be identified by the title of the information collection. Email address: infocollection@acf.hhs.gov. [Docket No. FDA–2012–N–0911] OMB Comment emcdonald on DSK67QTVN1PROD with NOTICES 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, Email: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2012–27583 Filed 11–13–12; 8:45 am] BILLING CODE 4184–01–P VerDate Mar<15>2010 14:41 Nov 13, 2012 Jkt 229001 Privacy Act of 1974; Report of a New System of Records; Food and Drug Administration User Fee System routine uses. The routine uses will become effective on December 31, 2012. Submit either electronic or written comments by December 31, 2012. ADDRESSES: You may submit comments, identified by Docket No. FDA–2012–N– 0911, by any of the following methods: records. Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. In accordance with the requirements of the Privacy Act of 1974 and the Food and Drug Administration’s (FDA) regulations for the protection of privacy, FDA is publishing notice of a Privacy Act system of records entitled, ‘‘FDA User Fee System, HHS/FDA,’’ System Number 09–10–0021. FDA utilizes the User Fee System (UFS) to collect fees pursuant to Federal law and FDA’s implementing regulations. The records kept in this system relate to fees assessed under the Freedom of Information Act (FOIA), the Prescription Drug User Fee Act, the Medical Device User Fee and Modernization Act, the Animal Drug User Fee Act, the Animal Generic Drug User Fee Act, the Mammography Quality Standards Act, the Family Smoking Prevention and Tobacco Control Act, the Food Safety Modernization Act, the Biosimilar User Fee Act, the Generic Drug User Fee Act, and other fees assessed by FDA under its Federal Food, Drug and Cosmetic Act authority such as color additive certification fees and export certificate fees. For purposes of this notice, these fees are collectively referred to as user fees. DATES: Effective Date: The new system of records will be effective on November 14, 2012, with the exception of the Written Submissions Submit written submissions in the following ways: • Fax: 301–827–6870. • Mail/Hand delivery/Courier (for paper or CD–ROM submissions): Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Instructions: All submissions received must include the Agency name and Docket No. FDA–2012–N–0911 for this notice. All comments received may be posted without change to https:// www.regulations.gov, including any personal information provided. For additional information on submitting comments, see the ‘‘Comments’’ heading of the SUPPLEMENTARY INFORMATION section of this document. Docket: For access to the docket to read background documents or comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Lisa Berry, Office of Financial Management, AGENCY: Food and Drug Administration, HHS. ACTION: Notice of a new system of SUMMARY: PO 00000 Frm 00031 Fmt 4703 Sfmt 4703 E:\FR\FM\14NON1.SGM 14NON1

Agencies

[Federal Register Volume 77, Number 220 (Wednesday, November 14, 2012)]
[Notices]
[Page 67820]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-27583]



[[Page 67820]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: 45 CFR 1303 Appeal Procedures for Head Start Grantees and 
Current or Prospective Delegate Agencies.
    OMB No.: 0980-0242.
    Description: Section 646 of the Head Start Act requires the 
Secretary to prescribe a timeline for conducting administrative 
hearings when adverse actions are taken or proposed against Head Start 
or Early Head Start grantees or delegate agencies. The Office of Head 
Start is proposing to renew without changes this rule which implements 
these requirements and which prescribe when a grantee must submit 
information and what that information should include to support a 
contention that adverse action should not be taken.
    Respondents: Head Start and Early Head Start grantees and delegate 
agencies against which the Head Start Bureau has taken or proposes to 
take adverse actions.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                  Number of     Average  burden
                 Instrument                      Number of      responses per      hours  per      Total burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
Appeal......................................              20                1               26              520
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 520

Additional Information

    Copies of the proposed collection may be obtained 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. All requests should be identified 
by the title of the information collection. Email 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, 
Email: OIRA_SUBMISSION@OMB.EOP.GOV.
    Attn: Desk Officer for the Administration for Children and 
Families.

Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012-27583 Filed 11-13-12; 8:45 am]
BILLING CODE 4184-01-P

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