Submission for OMB Review; Comment Request, 52331-52332 [2011-21316]
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Federal Register / Vol. 76, No. 162 / Monday, August 22, 2011 / Notices
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information: Price
Connor, PhD, NIOSH Health Scientist, 1600
Clifton Road, NE., Mailstop E–20, Atlanta,
Georgia 30333, Telephone (404) 498–2511,
Fax (404) 498–2571.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities for
both the Centers for Disease Control and
Prevention, and the Agency for Toxic
Substances and Disease Registry.
Dated: August 12, 2011.
Elizabeth Millington,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2011–21410 Filed 8–19–11; 8:45 am]
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requirements must be appropriate, i.e.,
meet all applicable MOE requirements.
The Annual MOE Report provides the
ability to learn about and to monitor the
nature of State and Territory
expenditures used to meet States and
Territories MOE requirements, and it is
an important source of information
about the different ways that States and
Territories are using their resources to
help families attain and maintain selfsufficiency. In addition, the report is
used to obtain State and Territory
program characteristics for ACFs annual
report to Congress, and the report serves
as a useful resource to use in
Congressional hearings about how
TANF programs are evolving, in
assessing State the Territory MOE
expenditures, and in assessing the need
for legislative changes.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Annual Report/ACF 204 (State
MOE)—1 collection.
OMB No.: 0970–0248.
Description
The Administration for Children and
Families (ACF) is requesting a threeyear extension of the ACF–204 (Annual
MOE Report). The report is used to
collect descriptive program
characteristics information on the
programs operated by States and
Territories in association with their
Temporary Assistance for Needy
Families (TANF) programs. All State
and Territory expenditures claimed
toward States and Territories MOE
Respondents
The 50 States of the United States, the
District of Columbia, Guam, Puerto
Rico, and the Virgin Islands.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
ACF–204 ..........................................................................................
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Instrument
54
1
128
6,912
Estimated Total Annual Burden
Hours: 6,912.
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 Planning, Research
and Evaluation, 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
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18:50 Aug 19, 2011
Jkt 223001
information to be collected; and (d)
ways to minimize the burden
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011–21317 Filed 8–19–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Frm 00029
Fmt 4703
Sfmt 4703
Authority to require States to submit
a State TANF plan is contained in
section 402 of the Social Security Act,
as amended by Public Law 104–193, the
Personal Responsibility and Work
Opportunity Reconciliation Act of 1996.
States are required to submit new plans
periodically (i.e., within a 27-month
period).
Respondents
Title: State Plan for the Temporary
Assistance for Needy Families (TANF).
PO 00000
The State plan is a mandatory
statement submitted to the Secretary of
the Department of Health and Human
Services by the State. It consists of an
outline specifying how the state’s TANF
program will be administered and
operated and certain required
certifications by the State’s Chief
Executive Officer. It is used to provide
the public with information about the
program.
We are proposing to continue the
information collection without change.
Submission for OMB Review;
Comment Request
OMB No.: 0970–0145.
Description
The 50 States of the United States, the
District of Columbia, Guam, Puerto
Rico, and the Virgin Islands.
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Federal Register / Vol. 76, No. 162 / Monday, August 22, 2011 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
Title Amendments ............................................................................
State TANF plan ..............................................................................
18
18
1
1
3
30
54
540
Estimated Total Annual Burden
Hours: 594.
ACTION:
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. 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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011–21316 Filed 8–19–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
jlentini on DSK4TPTVN1PROD with NOTICES
[Docket No. FDA–2011–N–0591]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Data To Support
Communications Usability Testing, as
Used by the Food and Drug
Administration
AGENCY:
Food and Drug Administration,
HHS.
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17:16 Aug 19, 2011
Jkt 223001
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by September
21, 2011.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–New and
title: ‘‘Data to Support Communications
Usability Testing, as Used by the Food
and Drug Administration.’’ Also include
the FDA docket number found in
brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Juanmanuel Vilela, Office of
Information Management, Food and
Drug Administration, 1350 Piccard Dr.,
PI50–400B, Rockville, MD 20850, 301–
796–7651,
Juanmanuel.vilela@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUMMARY:
Data To Support Communications
Usability Testing, as Used by the Food
and Drug Administration—(OMB
Control Number 0910–New)
FDA plans to use the data collected
under this generic clearance to inform
its communications campaigns on a
variety of topics related to products that
FDA regulates. FDA expects the data to
help staff message developers achieve
FDA communication objectives. FDA
also plans to use the data to help tailor
print, broadcast, and electronic media
communications in order for them to
have powerful and desired impacts on
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
target audiences. The data will not be
used for the purposes of making policy
or regulatory decisions.
The information collected will serve
two major purposes. First, as formative
research it will provide the critical
knowledge needed about target
audiences. FDA must explore
audiences’ beliefs, perceptions, and
decisionmaking processes on specific
topics in order to meet the basic
objectives of its risk communication
campaigns. Such knowledge will
provide the needed target audience
understanding to design effective
communication strategies, messages,
and product labels. These
communications will aim to improve
public understanding of the risks and
benefits of using various FDA-regulated
products by providing users with a
better context in which to place risk
information more completely.
Second, as pretesting, it will give FDA
some information about the potential
effectiveness of messages and materials
in reaching and successfully
communicating with their intended
audiences. Testing messages with a
sample of the target audience will allow
FDA to refine messages while still in the
developmental stage. Respondents may
be asked to give their reaction to the
messages in person or on-line.
FDA’s Centers and Offices will use
this mechanism to test the usability of
messages about FDA-regulated products
for consumers, patients, industry
representatives, or health care
professionals. The data will not be used
for the purposes of making policy or
regulatory decisions.
In the Federal Register of June 10,
2011 (76 FR 34083), FDA published a
60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
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Agencies
[Federal Register Volume 76, Number 162 (Monday, August 22, 2011)]
[Notices]
[Pages 52331-52332]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-21316]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: State Plan for the Temporary Assistance for Needy Families
(TANF).
OMB No.: 0970-0145.
Description
The State plan is a mandatory statement submitted to the Secretary
of the Department of Health and Human Services by the State. It
consists of an outline specifying how the state's TANF program will be
administered and operated and certain required certifications by the
State's Chief Executive Officer. It is used to provide the public with
information about the program.
Authority to require States to submit a State TANF plan is
contained in section 402 of the Social Security Act, as amended by
Public Law 104-193, the Personal Responsibility and Work Opportunity
Reconciliation Act of 1996. States are required to submit new plans
periodically (i.e., within a 27-month period).
We are proposing to continue the information collection without
change.
Respondents
The 50 States of the United States, the District of Columbia, Guam,
Puerto Rico, and the Virgin Islands.
[[Page 52332]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response
----------------------------------------------------------------------------------------------------------------
Title Amendments.................... 18 1 3 54
State TANF plan..................... 18 1 30 540
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 594.
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. 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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011-21316 Filed 8-19-11; 8:45 am]
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