Proposed Information Collection Activity; Comment Request, 60129 [2010-24212]

Download as PDF 60129 Federal Register / Vol. 75, No. 188 / Wednesday, September 29, 2010 / Notices Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) The accuracy of the agency’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 those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. Direct Comments to OMB: Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the: Office of Management and Budget, Office of Regulatory Affairs, OIRA_submission@omb.eop.gov or by fax to 202–395–6974, Attention: Desk Officer for NIH. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Dr. Cathrine Sasek, Coordinator, Science Education Program, Office of Science Policy and Communications, National Institute on Drug Abuse, 6001 Executive Blvd, Room 5237, Bethesda, MD 20892, or call non-toll-free number (301) 443– 6071; fax (301) 443–6277; or by e-mail to csasek@nida.nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 30-days of the date of this publication. Dated: September 22, 2010. Mary Affeldt, Executive Officer, (OM Director, NIDA). [FR Doc. 2010–24400 Filed 9–28–10; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Proposed Projects Title: Required Data Elements for Paternity Establishment Affidavits. OMB No.: 0970–0171. Description: Section 466(a)(5)(C)(iv) of the Social Security Act the Act) requires States to develop and use an affidavit for the voluntary acknowledgement of paternity. The affidavit for the voluntary acknowledgement of paternity must include the minimum requirements specified by the Secretary under section 452(a)(7) of the Act. The affidavits will be used by hospitals, birth record agencies, and other entities participating in the voluntary paternity establishment program. Respondents: State and Tribal IV–D agencies, hospitals, birth record agencies and other entities participating in the voluntary paternity establishment program. ANNUAL BURDEN ESTIMATES Number of respondents erowe on DSK5CLS3C1PROD with NOTICES Instrument Estimated Total Annual Burden Hours: 0 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 Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail 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 VerDate Mar<15>2010 15:17 Sep 28, 2010 Jkt 220001 Number of responses per respondent Average burden hours per response Total burden hours 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 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. DEPARTMENT OF HEALTH AND HUMAN SERVICES Dated: September 22, 2010. Robert Sargis, Reports Clearance Officer. HHS. PO 00000 Frm 00065 Fmt 4703 Sfmt 4703 [Docket No. FDA–2010–D–0482] Draft Guidance for Industry and Investigators on Safety Reporting Requirements for Investigational New Drug Applications and Bioavailability/ Bioequivalence Studies; Availability AGENCY: ACTION: [FR Doc. 2010–24212 Filed 9–28–10; 8:45 am] BILLING CODE 4184–01–P Food and Drug Administration Food and Drug Administration, Notice. The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry and investigators entitled ‘‘Safety Reporting Requirements for INDs and BA/BE Studies.’’ This draft guidance is intended to help sponsors and investigators comply with the new requirements in the final rule entitled ‘‘Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products and Safety SUMMARY: E:\FR\FM\29SEN1.SGM 29SEN1

Agencies

[Federal Register Volume 75, Number 188 (Wednesday, September 29, 2010)]
[Notices]
[Page 60129]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24212]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

Proposed Projects

    Title: Required Data Elements for Paternity Establishment 
Affidavits.
    OMB No.: 0970-0171.
    Description: Section 466(a)(5)(C)(iv) of the Social Security Act 
the Act) requires States to develop and use an affidavit for the 
voluntary acknowledgement of paternity. The affidavit for the voluntary 
acknowledgement of paternity must include the minimum requirements 
specified by the Secretary under section 452(a)(7) of the Act. The 
affidavits will be used by hospitals, birth record agencies, and other 
entities participating in the voluntary paternity establishment 
program.
    Respondents: State and Tribal IV-D agencies, hospitals, birth 
record agencies and other entities participating in the voluntary 
paternity establishment program.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                   Instrument                        Number of     responses per     hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
                                                  ..............  ..............  ..............  ..............
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 0
    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 
Administration, Office of Information Services, 370 L'Enfant Promenade, 
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail 
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 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.

    Dated: September 22, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-24212 Filed 9-28-10; 8:45 am]
BILLING CODE 4184-01-P