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