Proposed Information Collection Activity; Comment Request, 58996-58997 [2012-23528]
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58996
Federal Register / Vol. 77, No. 186 / Tuesday, September 25, 2012 / Notices
consider all timely and responsive
public comments that it receives on or
before October 25, 2012. You can find
more information, including routine
uses permitted by the Privacy Act, in
the Commission’s privacy policy, at
https://www.ftc.gov/ftc/privacy.htm.
Comments on the information
collection requirements subject to
review under the PRA should
additionally be submitted to OMB. If
sent by U.S. mail, they should be
addressed to Office of Information and
Regulatory Affairs, Office of
Management and Budget, Attention:
Desk Officer for the Federal Trade
Commission, New Executive Office
Building, Docket Library, Room 10102,
725 17th Street NW., Washington, DC
20503. Comments sent to OMB by U.S.
postal mail, however, are subject to
delays due to heightened security
precautions. Thus, comments instead
should be sent by facsimile to (202)
395–5167.
Willard K. Tom,
General Counsel.
[FR Doc. 2012–23524 Filed 9–24–12; 8:45 am]
BILLING CODE 6750–01–P
GENERAL SERVICES
ADMINISTRATION
[Notice-QDA–2012–01; Docket No. 2012–
0002; Sequence 17]
Multiple Award Schedule (MAS)
Program Continuous Open Season—
Operational Change; Extension of
Comment Period
Federal Acquisition Service
(FAS), General Services Administration
(GSA).
ACTION: Notice with a request for
comments; extension of comment
period.
AGENCY:
The General Services
Administration (GSA), Federal
Acquisition Service (FAS) issued a
notice on July 23, 2012. The comment
period is extended to provide additional
SUMMARY:
time for interested parties to the review
and submit comments on the notice.
DATES: The comment period for the
notice published in the Federal Register
at 77 FR 43084, July 23, 2012, is
extended for 30 days after publication in
the Federal Register.
This change in operations will
become effective 60 days after
publication in the Federal Register.
Comment Date: Interested parties
should submit written comments to the
Regulatory Secretariat at one of the
addressees shown below on or before 30
days after publication in the Federal
Register. This will allow GSA sufficient
time to consider the comments prior to
the effective date of this notice.
ADDRESSES: Submit comments in
response to Notice-QDA–2012–01 by
any of the following methods:
• Regulations.gov: https://www.
regulations.gov. Submit comments via
the Federal eRulemaking portal by
searching for ‘‘Notice-QDA–2012–01’’.
Select the link ‘‘Submit a Comment’’
that corresponds with ‘‘Notice-QDA–
2012–01.’’ Follow the instructions
provided at the ‘‘Submit a Comment’’
screen. Please include your name,
company name (if any), and ‘‘NoticeQDA–2012–01’’ on your attached
document.
• FAX: (202) 501–4067.
• Mail: General Services
Administration, Regulatory Secretariat
(MVCB), ATTN: Hada Flowers, 1275
First Street NE., 7th Floor, Washington,
DC 20417.
Instructions: Please submit comments
only and cite Notice-QDA–2012–01, in
all correspondence related to this case.
All comments received will be posted
without change to https://www.
regulations.gov, including any personal
and/or business confidential
information provided.
FOR FURTHER INFORMATION CONTACT: Mrs.
Angela Lehman, telephone 703–605–
9541, email DemandBasedModel@gsa.
gov.
The
General Services Administration (GSA),
SUPPLEMENTARY INFORMATION:
Federal Acquisition Service (FAS)
published a notice in the Federal
Register at 77 FR 43084, July 23, 2012.
The comment period is extended to
provide additional time for interested
parties to the review and submit
comments on the notice.
Dated: September 12, 2012.
Houston Taylor,
Assistant Commissioner, Office of Acquisition
Management, Federal Acquisition Service,
General Services Administration.
[FR Doc. 2012–23607 Filed 9–24–12; 8:45 am]
BILLING CODE 6820–89–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: State Self-Assessment Review
and Report.
OMB No.: 0970–0223.
Description: Section 454(15)(A) of the
Social Security Act, as amended by the
Personal Responsibility and Work
Opportunity Reconciliation Act of 1996,
requires each State to annually assess
the performance of its child support
enforcement program in accordance
with standards specified by the
Secretary of the Department of Health
and Human Services, and to provide a
report of the findings to the Secretary.
This information is required to
determine if States are complying with
Federal child support mandates and
providing the best services possible. The
report is also intended to be used as a
management tool to help States evaluate
their programs and assess performance.
Respondents: State Child Support
Enforcement Agencies or the
Department/Agency/Bureau responsible
for Child Support Enforcement in each
State.
ANNUAL BURDEN ESTIMATES
emcdonald on DSK67QTVN1PROD with NOTICES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Self-assessment report ....................................................................................
54
1
4
216
Estimated Total Annual Burden
Hours: 216.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
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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
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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
E:\FR\FM\25SEN1.SGM
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Federal Register / Vol. 77, No. 186 / Tuesday, September 25, 2012 / Notices
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email 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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012–23528 Filed 9–24–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0980]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Guidance on
Reagents for Detection of Specific
Novel Influenza A Viruses
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
guidance on reagents for detection of
specific novel influenza A viruses.
DATES: Submit either electronic or
written comments on the collection of
information by November 26, 2012.
ADDRESSES: Submit electronic
comments on the collection of
emcdonald on DSK67QTVN1PROD with NOTICES
SUMMARY:
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14:15 Sep 24, 2012
Jkt 226001
information to https://www.regulations.
gov. Submit written comments on the
collection of information to the Division
of Dockets Management (HFA–305),
Food and Drug Administration, 5630
Fishers Lane, Rm. 1061, Rockville, MD
20852. All comments should be
identified with the docket number
found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Daniel Gittleson, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
5156, Daniel.Gittleson@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’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
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Guidance on Reagents for Detection of
Specific Novel Influenza A Viruses—
(OMB Control Number 0910–0584)—
Extension
In accordance with section 513 of the
Federal Food, Drug, and Cosmetic Act
(the FD&C Act) (21 U.S.C. 360c), FDA
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58997
evaluated an application for an in vitro
diagnostic device for detection of
influenza subtype H5 (Asian lineage),
commonly known as avian flu. FDA
concluded that this device is properly
classified into class II in accordance
with 21 U.S.C. 360c(a)(1)(B), because it
is a device for which the general
controls by themselves are insufficient
to provide reasonable assurance of the
safety and effectiveness of the device,
but there is sufficient information to
establish special controls to provide
such assurance. The statute permits
FDA to establish as special controls
many different things, including
postmarket surveillance, development
and dissemination of guidance
recommendations, and ‘‘other
appropriate actions as the Secretary
deems necessary’’ (21 U.S.C.
360c(a)(1)(B)). This information
collection is a measure that FDA
determined to be necessary to provide
reasonable assurance of safety and
effectiveness of reagents for detection of
specific novel influenza A viruses.
FDA issued an order classifying the
H5 (Asian lineage) diagnostic device
into class II on February 3, 2006,
establishing the special controls
necessary to provide reasonable
assurance of the safety and effectiveness
of that device and similar future
devices. The new classification was
codified in 21 CFR 866.3332, a
regulation that describes the new
classification for reagents for detection
of specific novel influenza A viruses
and sets forth the special controls that
help to provide a reasonable assurance
of the safety and effectiveness of devices
classified under that regulation. The
regulation refers to the special controls
guidance document entitled ‘‘Class II
Special Controls Guidance Document:
Reagents for Detection of Specific Novel
Influenza A Viruses,’’ which provides
recommendations for measures to help
provide a reasonable assurance of safety
and effectiveness for these reagents. The
guidance document recommends that
sponsors obtain and analyze postmarket
data to ensure the continued reliability
of their device in detecting the specific
novel influenza A virus that it is
intended to detect, particularly given
the propensity for influenza viruses to
mutate and the potential for changes in
disease prevalence over time. As
updated sequences for novel influenza
A viruses become available from the
World Health Organization, National
Institutes of Health, and other public
health entities, sponsors of reagents for
detection of specific novel influenza A
viruses will collect this information,
compare them with the primer/probe
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]]>Agencies
[Federal Register Volume 77, Number 186 (Tuesday, September 25, 2012)]
[Notices]
[Pages 58996-58997]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-23528]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: State Self-Assessment Review and Report.
OMB No.: 0970-0223.
Description: Section 454(15)(A) of the Social Security Act, as
amended by the Personal Responsibility and Work Opportunity
Reconciliation Act of 1996, requires each State to annually assess the
performance of its child support enforcement program in accordance with
standards specified by the Secretary of the Department of Health and
Human Services, and to provide a report of the findings to the
Secretary. This information is required to determine if States are
complying with Federal child support mandates and providing the best
services possible. The report is also intended to be used as a
management tool to help States evaluate their programs and assess
performance.
Respondents: State Child Support Enforcement Agencies or the
Department/Agency/Bureau responsible for Child Support Enforcement in
each State.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Self-assessment report...................... 54 1 4 216
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 216.
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
[[Page 58997]]
Promenade SW., Washington, DC 20447, Attn: ACF Reports Clearance
Officer. Email 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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012-23528 Filed 9-24-12; 8:45 am]
BILLING CODE 4184-01-P
