Submission for OMB Review; Comment Request, 34999 [2011-14627]
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34999
Federal Register / Vol. 76, No. 115 / Wednesday, June 15, 2011 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Work Participation and TANF/
WIA Coordination Project.
OMB No.: New collection.
Description: The Administration for
Children and Families (ACF) is
proposing an information collection
activity as part of the Work Participation
and TANF/WIA Coordination Project.
The proposed information collection
consists of semi-structured interviews
with key state/and or local Temporary
Assistance for Needy Families (TANF)
and Work Investment Act (WIA)
respondents on questions of engagement
in additional work activities and
expenditures of other benefits and
services as well as questions concerning
TANF/WIA Coordination. Through this
information collection, ACF seeks to
elucidate the data presented in reports
submitted by states to the ACF Office of
Family Assistance (OFA) as required by
the Claims Resolution Act of 2010. This
collection is separate from the state
reports to OFA required by the Act. In
addition, it will provide documentation
of positive TANF/WIA coordination
activities.
Respondents: State and/or local
administrators responsible for the TANF
and WIA Programs.
ANNUAL BURDEN ESTIMATES
Instrument
Annual
number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total annual
burden hours
Discussion Guide for Use with State TANF officials .......................................
40
2
8
640
Estimated Total Annual Burden
Hours: 640.
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: OPRE Reports
Clearance Officer. All requests should
be identified by the title of the
information collection. E-mail address:
OPREinfocollection@acf.hhs.gov.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
OMB Comment
AGENCY:
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–
395–6974 Attn: Desk Officer for the
Administration for Children and
Families.
HHS.
Dated: June 7, 2011.
Steven M. Hanmer,
OPRE Reports Clearance Officer.
jlentini on DSK4TPTVN1PROD with NOTICES
[FR Doc. 2011–14627 Filed 6–14–11; 8:45 am]
BILLING CODE 4184–09–M
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18:12 Jun 14, 2011
Jkt 223001
Food and Drug Administration
[Docket No. FDA–2011–D–0378]
Draft Guidance for Industry and Food
and Drug Administration Staff;
Establishing the Performance
Characteristics of In Vitro Diagnostic
Devices for the Detection of
Methicillin-Resistant Staphylococcus
Aureus for Culture-Based Devices;
Availability
ACTION:
Food and Drug Administration,
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability of the draft guidance
entitled ‘‘Establishing the Performance
Characteristics of In Vitro Diagnostic
Devices for the Detection of MethicillinResistant Staphylococcus Aureus for
Culture-Based Devices.’’ This draft
guidance document provides industry
and Agency staff with recommendations
for studies for establishing the
performance characteristics of in vitro
diagnostic devices for the detection of
methicillin-resistant S. aureus (MRSA),
including those for the detection or
detection and differentiation of MRSA
versus S. aureus (SA) in either human
specimens or bacterial growth detected
by continuous monitoring blood culture
systems. This draft guidance is not final
nor is it in effect at this time.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
SUMMARY:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
either electronic or written comments
on the draft guidance by September 13,
2011.
ADDRESSES: Submit written requests for
single copies of the draft guidance
document entitled ‘‘Establishing the
Performance Characteristics of In Vitro
Diagnostic Devices for the Detection of
Methicillin-Resistant Staphylococcus
Aureus (MRSA) for Culture-Based
Devices’’ to the Division of Small
Manufacturers, International, and
Consumer Assistance, Center for
Devices and Radiological Health, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 66, rm. 4613,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist that office in processing your
request, or fax your request to 301–847–
8149. See the SUPPLEMENTARY
INFORMATION section for information on
electronic access to the guidance.
Submit electronic comments on the
draft guidance to https://
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Identify
comments with the docket number
found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Alexandra Wong, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, rm. 5502, Silver Spring,
MD 20993–0002, 301–796–6210.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is issuing this draft guidance to
provide industry and Agency staff with
recommendations for studies for
establishing the performance
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15JNN1
Agencies
[Federal Register Volume 76, Number 115 (Wednesday, June 15, 2011)]
[Notices]
[Page 34999]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-14627]
[[Page 34999]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Work Participation and TANF/WIA Coordination Project.
OMB No.: New collection.
Description: The Administration for Children and Families (ACF) is
proposing an information collection activity as part of the Work
Participation and TANF/WIA Coordination Project. The proposed
information collection consists of semi-structured interviews with key
state/and or local Temporary Assistance for Needy Families (TANF) and
Work Investment Act (WIA) respondents on questions of engagement in
additional work activities and expenditures of other benefits and
services as well as questions concerning TANF/WIA Coordination. Through
this information collection, ACF seeks to elucidate the data presented
in reports submitted by states to the ACF Office of Family Assistance
(OFA) as required by the Claims Resolution Act of 2010. This collection
is separate from the state reports to OFA required by the Act. In
addition, it will provide documentation of positive TANF/WIA
coordination activities.
Respondents: State and/or local administrators responsible for the
TANF and WIA Programs.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Annual number responses per hours per Total annual
of respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Discussion Guide for Use with State TANF 40 2 8 640
officials..................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 640.
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: OPRE Reports Clearance Officer. All
requests should be identified by the title of the information
collection. E-mail address: OPREinfocollection@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:
202-395-6974 Attn: Desk Officer for the Administration for Children and
Families.
Dated: June 7, 2011.
Steven M. Hanmer,
OPRE Reports Clearance Officer.
[FR Doc. 2011-14627 Filed 6-14-11; 8:45 am]
BILLING CODE 4184-09-M