Agency Information Collection Activities; Proposed Collection; Public Comment Request, 18982-18983 [2013-07144]
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18982
Federal Register / Vol. 78, No. 60 / Thursday, March 28, 2013 / Notices
The 1364C captures an offeror’s
proposed interest rate and amortization
period for the tenant improvements, in
addition to the lessor’s overhead fees.
The Succeeding and Superseding
Lease Model uses GSA Form 1364D.
These leases are negotiated with the
existing lessor after advertisements and
cost benefit analyses result in a
determination that such a lease is in the
best interests of the government. The
form has less data input required than
for a Standard lease; it also includes
current rental rate information, supplied
by the Government.
The 1364A–1, 1364B, and 1364C
summarize an offeror’s technical
compliance with some important
statutory and regulatory requirements to
make the overall offer process easier for
offerors to understand (e.g., accessibility
and seismic standards, flood plain
compliance, asbestos). The 1364C also
limits the collection of tenant
improvement overhead fees to the
architect/engineering fees and lessor’s
project management fees. A notice was
published in the Federal Register at 78
FR 303, on January 3, 2013. No
comments were received.
B. Annual Reporting Burden
Respondents: 3565.
Responses per Respondent: 1.
Total Responses: 3565.
Hours per Response: 2.4238 (average).
Total Burden Hours: 8641.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat, 1275 First Street
NE., Washington, DC 20417, telephone
(202) 501–4755. Please cite OMB
Control No. 3090–0086, GSA Form
1364, Proposal to Lease Space, in all
correspondence.
Dated: March 20, 2013.
Joseph A. Neurauter,
Director, Office of Acquisition Policy & Senior
Procurement Executive (MV).
[FR Doc. 2013–07249 Filed 3–27–13; 8:45 am]
BILLING CODE 6820–61–P
mstockstill on DSK4VPTVN1PROD with NOTICES
GENERAL SERVICES
ADMINISTRATION
[Notice-FTR 2013–01; Docket 2013–0002;
Sequence 7]
Maximum Per Diem Rates for the
States of Oklahoma and Texas
Notice of Per Diem Bulletin 13–
04, revised continental United States
(CONUS) per diem rates.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
SUMMARY: The General Services
Administration (GSA) has conducted its
mid-year review and has determined
that the per diem rates for certain
locations in the States of Oklahoma and
Texas are inadequate.
[Document Identifier HHS–OS–19158–60D]
Effective date: This notice is
effective April 1, 2013 and applies to
travel performed on or after April 1,
2013.
ACTION:
ACTION:
DATES:
For
clarification of content, please contact
Ms. Jill Denning, Office of
Governmentwide Policy, Office of Asset
and Transportation Management, at
202–208–7642, or by email at
travelpolicy@gsa.gov. Please cite Notice
of FTR Bulletin 13–04.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
A. Background
After an analysis of the per diem rates
established for FY 2013 (see the Federal
Register notice at 77 FR 54578,
September 5, 2012, and FTR Bulletin
13–01), non-standard area per diem
rates are being established for the
following locations:
State of Oklahoma
• Garfield County
State of Texas
• Midland County
CONUS per diem rates are published
as FTR per diem bulletins available on
the Internet at www.gsa.gov/perdiem
and www.gsa.gov/bulletins. This process
ensures timely notice of increases or
decreases in per diem rates established
by GSA for Federal employees on
official travel within CONUS. Notices
published periodically in the Federal
Register, such as this one, now
constitute the only notification of
revisions in CONUS per diem rates to
agencies.
Dated: March 22, 2013.
Craig J. Flynn,
Acting Deputy Director, Office of Asset and
Transportation Management, Office of
Governmentwide Policy.
[FR Doc. 2013–07243 Filed 3–27–13; 8:45 am]
BILLING CODE 6820–14–P
Office of Governmentwide
Policy (OGP), General Services
Administration (GSA).
AGENCY:
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Office of the Secretary
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
Notice.
AGENCY:
SUMMARY: In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to submit a new Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting that ICR to
OMB, OS seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on the ICR must be
received on or before May 28, 2013.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
document identifier HHS–OS–19158–
60D for reference.
Information Collection Request Title:
Doing It For Ourselves (DIFO) Program.
Abstract: The Office of Women’s
Health (OWH) and the Department of
Health and Human Services (HHS)
Coordinating Committee on Lesbian,
Gay, Bi-sexual and Transgender (LGBT)
Issues have prioritized the collection of
health data on LGBT populations. In
response, OWH funded an initiative to
identify and test effective and
innovative ways of reducing obesity in
lesbian and bisexual women. The DIFO
intervention has been developed in San
Francisco to address what is known
about local LB women’s community
norms, common barriers to health,
patterns of physical and mental health
access, and preferences for health
services and health outcomes. The
evaluation of the DIFO program will
address the following research question:
Does an intervention based on an
ecological model of LB women’s health
result in improved health, as defined by:
quality of life, decreased weight,
improved nutrition, and increased
physical activity? The project is
scheduled for one year.
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Federal Register / Vol. 78, No. 60 / Thursday, March 28, 2013 / Notices
Need and Proposed Use of the
Information: Addresses barriers to
health for the LB community, and
promotes overall health and wellbeing.
The intervention will incorporate
community-identified weight loss/risk
reduction needs of this population.
Following the completion of the surveys
and interventions, collected data will be
used to develop increased health-related
services and activities for LB women,
web-based tools and materials for LB
women, increased community
recreation resources inclusive of sexual
minority women.
Likely Respondents: Lesbian and bisexual women forty years of age and
older.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions, to
develop, acquire, install and utilize
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information, to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information, and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of respondents
Number of responses per
respondent
Average burden hours per
response
Screening Tool .................................................................................................
Informed Consent Form ...................................................................................
Baseline Survey ...............................................................................................
Baseline Comparison Survey ..........................................................................
9 Month Follow-up Survey ...............................................................................
9- Month Follow-Up Comparison Survey ........................................................
End-of-Program Focus Group .........................................................................
300
256
128
128
128
128
128
1
1
1
1
1
1
1
5/60
5/60
5/60
5/60
5/60
5/60
1
25
21
11
11
11
11
128
Total ..........................................................................................................
........................
........................
........................
218
Forms
OS specifically requests comments on
(1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013–07144 Filed 3–27–13; 8:45 am]
BILLING CODE 4150–33–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to Ron Otten, 1600 Clifton
Road, MS–D74, Atlanta, GA 30333 or
send an email to omb@cdc.gov.
Comments are invited 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)
ways to enhance 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. Written comments should
be received within 60 days of this
notice.
Proposed Project
Proposed Data Collections Submitted
for Public Comment and
Recommendations
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[60Day-13–13OE]
Cytology Workload Assessment and
Measure—New—Office of Surveillance,
Epidemiology and Laboratory (OSELS),
Centers for Disease Control and
Prevention (CDC).
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
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Background and Brief Description
CDC provides technical guidance to
the Department of Health and Human
Services (HHS) in coordination with the
Centers for Medicare & Medicaid
Services (CMS) and the Food and Drug
Administration (FDA) for the
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Total burden
hours
implementation of the Clinical
Laboratory Improvement Amendments
(CLIA). The Clinical Laboratory
Improvement Amendments of 1988
directed the Secretary of Health and
Human Services to establish the
maximum number of cytology slides
that any individual may screen in a 24
hour period; to establish certain quality
assurance standards; to set personnel
standards; and to provide for periodic
proficiency testing of cytotechnologists
and pathologists involved in screening
and interpreting cytological
preparations. The regulations
implementing CLIA, published in the
Federal Register of February 28, 1992,
established that the maximum number
of slides examined by an individual in
each 24 hour period was not to exceed
100 slides and could not be examined
in less than an eight-hour day. The
regulation further established that the
technical supervisor is required to
evaluate the performance of
cytotechnologists at least every six
months and determine their individual
maximum daily workload limit. CDC
requests OMB approval to collect
information on cytology workload
practice assessment through a survey on
workflow and performance practices of
cytotechnologists. Clearance is being
requested for one year.
In 1992, when the regulation was
published, all Pap slides were
conventional ‘‘Pap smears.’’ In a
conventional Pap smear, samples are
smeared directly onto a glass
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]]>Agencies
[Federal Register Volume 78, Number 60 (Thursday, March 28, 2013)]
[Notices]
[Pages 18982-18983]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-07144]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier HHS-OS-19158-60D]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Secretary (OS), Department of
Health and Human Services, announces plans to submit a new Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting that ICR to OMB, OS seeks
comments from the public regarding the burden estimate, below, or any
other aspect of the ICR.
DATES: Comments on the ICR must be received on or before May 28, 2013.
ADDRESSES: Submit your comments to
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the document identifier HHS-OS-19158-60D
for reference.
Information Collection Request Title: Doing It For Ourselves (DIFO)
Program.
Abstract: The Office of Women's Health (OWH) and the Department of
Health and Human Services (HHS) Coordinating Committee on Lesbian, Gay,
Bi-sexual and Transgender (LGBT) Issues have prioritized the collection
of health data on LGBT populations. In response, OWH funded an
initiative to identify and test effective and innovative ways of
reducing obesity in lesbian and bisexual women. The DIFO intervention
has been developed in San Francisco to address what is known about
local LB women's community norms, common barriers to health, patterns
of physical and mental health access, and preferences for health
services and health outcomes. The evaluation of the DIFO program will
address the following research question: Does an intervention based on
an ecological model of LB women's health result in improved health, as
defined by: quality of life, decreased weight, improved nutrition, and
increased physical activity? The project is scheduled for one year.
[[Page 18983]]
Need and Proposed Use of the Information: Addresses barriers to
health for the LB community, and promotes overall health and wellbeing.
The intervention will incorporate community-identified weight loss/risk
reduction needs of this population. Following the completion of the
surveys and interventions, collected data will be used to develop
increased health-related services and activities for LB women, web-
based tools and materials for LB women, increased community recreation
resources inclusive of sexual minority women.
Likely Respondents: Lesbian and bi-sexual women forty years of age
and older.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions, to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information, to train personnel and to be able to respond to
a collection of information, to search data sources, to complete and
review the collection of information, and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Forms Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Screening Tool.................................. 300 1 5/60 25
Informed Consent Form........................... 256 1 5/60 21
Baseline Survey................................. 128 1 5/60 11
Baseline Comparison Survey...................... 128 1 5/60 11
9 Month Follow-up Survey........................ 128 1 5/60 11
9- Month Follow-Up Comparison Survey............ 128 1 5/60 11
End-of-Program Focus Group...................... 128 1 1 128
---------------------------------------------------------------
Total....................................... .............. .............. .............. 218
----------------------------------------------------------------------------------------------------------------
OS specifically requests comments on (1) the necessity and utility
of the proposed information collection for the proper performance of
the agency's functions, (2) the accuracy of the estimated burden, (3)
ways to enhance the quality, utility, and clarity of the information to
be collected, and (4) the use of automated collection techniques or
other forms of information technology to minimize the information
collection burden.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013-07144 Filed 3-27-13; 8:45 am]
BILLING CODE 4150-33-P
