Information Collection; Commercial Item Acquisitions, 43201-43202 [2016-15703]
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Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices
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Dated: June 28, 2016.
James R. Park,
Executive Director.
[FR Doc. 2016–15672 Filed 6–30–16; 8:45 am]
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Federal Communications Commission.
Marlene H. Dortch,
Secretary.
DEPARTMENT OF DEFENSE
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GENERAL SERVICES
ADMINISTRATION
FEDERAL FINANCIAL INSTITUTIONS
EXAMINATION COUNCIL
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[Docket No. AS16–07]
[OMB Control No. 9000–0136; Docket 2016–
0053; Sequence 28]
Appraisal Subcommittee Notice of
Meeting
Appraisal Subcommittee of the
Federal Financial Institutions
Examination Council.
ACTION: Notice of meeting.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
AGENCY:
Description: In accordance with
Section 1104 (b) of Title XI of the
Financial Institutions Reform, Recovery,
and Enforcement Act of 1989, as
amended, notice is hereby given that the
Appraisal Subcommittee (ASC) will
meet in open session for its regular
meeting:
Location: Federal Reserve Board—
International Square location, 1850 K
Street NW., Washington, DC 20006.
Date: July 13, 2016.
Time: 10:00 a.m.
Status: Open.
Reports
Chairman
Executive Director
VerDate Sep<11>2014
19:05 Jun 30, 2016
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Information Collection; Commercial
Item Acquisitions
Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice of request for comments
regarding an extension to an existing
OMB clearance.
AGENCY:
Under the provisions of the
Paperwork Reduction Act, the
Regulatory Secretariat Division will be
submitting to the Office of Management
and Budget (OMB) a request to review
and approve an extension of a
previously approved information
collection requirement concerning the
clauses and provisions required for use
in commercial item acquisitions.
DATES: Submit comments on or before
August 30, 2016.
SUMMARY:
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43201
Submit comments
identified by Information Collection
9000–0136, Commercial Item
Acquisitions, by any of the following
methods:
• Regulations.gov: https://
www.regulations.gov.
Submit comments via the Federal
eRulemaking portal by searching the
OMB control number. Select the link
‘‘Submit a Comment’’ that corresponds
with ‘‘Information Collection 9000–
0136, Commercial Item Acquisitions’’.
Follow the instructions provided at the
‘‘Submit a Comment’’ screen. Please
include your name, company name (if
any), and ‘‘Information Collection 9000–
0136, Commercial Item Acquisitions’’
on your attached document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), 1800 F Street NW.,
Washington, DC 20405. ATTN: Ms.
Flowers/IC 9000–0136, Commercial
Item Acquisitions.
Instructions: Please submit comments
only and cite Information Collection
9000–0136, Commercial Item
Acquisitions, in all correspondence
related to this collection. Comments
received generally will be posted
without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two to three days after
submission to verify posting (except
allow 30 days for posting of comments
submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr.
Michael O. Jackson, Procurement
Analyst, Office of Governmentwide
Acquisition Policy, GSA, at 202–208–
4949, or email at
michaelo.jackson@gsa.gov.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
A. Purpose
The Federal Acquisition Streamlining
Act of 1994 reformed Federal
acquisition statutes to encourage and
facilitate the acquisition of commercial
items and services by the Federal
Government. Accordingly, DoD, NASA,
and GSA amended the Federal
Acquisition Regulation (FAR) to include
streamlined/simplified procedures for
the acquisition of commercial items.
Pertinent to this information
collection, FAR Provision 52.212–3,
‘‘Offeror Representations and
Certifications—Commercial Items,’’ was
implemented to combine the multitude
of individual provisions used in
Government solicitations into a single
provision for use in commercial
E:\FR\FM\01JYN1.SGM
01JYN1
43202
Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices
acquisitions. The provision is among the
representations and certifications that
are available for completion in the
System for Award Management (SAM).
B. Annual Reporting Burden
Respondents: 397,000.
Responses per Respondent: 1.46.
Total Responses: 579,620.
Hours per Response: .500.
Total Burden Hours: 289,810.
Frequency: On Occasion.
Affected Public: Businesses or other
for-profit and not-for-profit institutions.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the Federal
Acquisition Regulations (FAR), and
whether it will have practical utility;
whether our estimate of the public
burden of this collection of information
is accurate, and based on valid
assumptions and methodology; ways to
enhance the quality, utility, and clarity
of the information to be collected; and
ways in which we can minimize the
burden of the collection of information
on those who are to respond, through
the use of appropriate technological
collection techniques or other forms of
information technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755.
Please cite OMB Control No. 9000–
0136 regarding Commercial Item
Acquisitions in all correspondence.
Dated: June 28, 2016.
Mahruba Uddowla,
Acting Director, Federal Acquisition Policy
Division, Office of Governmentwide
Acquisition Policy, Office of Acquisition
Policy, Office of Governmentwide Policy.
Proposed Project
National Amyotrophic Lateral Sclerosis
(ALS) Registry—Revision—Agency for
Toxic Substances and Disease Registry
(ATSDR)
[FR Doc. 2016–15703 Filed 6–30–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Agency for Toxic Substances and
Disease Registry
[30Day–16–0041]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Agency for Toxic Substances and
Disease Registry (ATSDR) has submitted
the following information collection
request to the Office of Management and
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19:05 Jun 30, 2016
Jkt 238001
Budget (OMB) for review and approval
in accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, Washington, DC 20503 or by fax
to (202) 395–5806. Written comments
should be received within 30 days of
this notice.
Background and Brief Description
On October 10, 2008, President Bush
signed S. 1382: ALS Registry Act which
amended the Public Health Service Act
to provide for the establishment of an
Amyotrophic Lateral Sclerosis (ALS)
Registry. The activities described are
part of the ongoing effort to maintain the
National ALS Registry.
First approved in 2010 for selfregistration, the primary goal of the
surveillance system/registry remains to
obtain reliable information on the
incidence and prevalence of ALS and to
better describe the demographic
characteristics (age, race, sex, and
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geographic location) of persons with
ALS (PALS). Those interested in
participating in the National ALS
Registry must answer a series of
validation questions and if determined
to be eligible they can register.
The secondary goal of the surveillance
system/registry is to collect additional
information on potential risk factors for
ALS, including, but not limited to,
family history of ALS, smoking history,
military service, residential history, lifetime occupational exposure, home
pesticide use, hobbies, hormonal and
reproductive history (women only),
caffeine use, trauma, health insurance,
open-ended supplemental questions,
and clinical signs and symptoms. After
registration, participants complete as
many as 16 voluntary survey modules,
each taking five minutes (maximum 80
minutes). In addition, in Year 1, a
disease progression survey for new
registrants is completed at 0, 3, and 6
months. In Years 2 and 3, the disease
progression survey is repeated at the
yearly anniversary and at 6 months. For
burden estimation, the number of
disease progression survey responses
per year has been rounded up to 3
times.
A biorepository component is being
added to increase the value of the
National ALS Registry to researchers. As
part of registration the participant can
request additional information about the
biorepository and provide additional
contact information. A geographically
representative sample will be selected to
provide specimens. There are two types
of specimen collections, in-home and
postmortem. The in-home collection
includes blood, urine, hair and nails.
The postmortem collection includes the
brain, spinal cord, cerebral spinal fluid
(CSF), bone, muscle, and skin.
In addition to fulfilling the two-part
Congressional mandate, the Registry is
designed to be a tool for ALS
researchers. Now that the Registry has
matured, ATSDR will make data and
specimens available to researchers.
They can request access to specimens,
data, or both collected by the National
ALS Registry for their research projects.
ATSDR will review applications for
scientific validity and human subjects
protection and make data/specimens
available to approved researchers.
ATSDR is also collaborating with ALS
service organizations to conduct
outreach activities through their local
chapters and districts as well as on a
national level. They will provide
ATSDR with information on their
outreach efforts in support of the
Registry on a monthly basis.
There are no costs to the respondents
other than their time. The total number
E:\FR\FM\01JYN1.SGM
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Agencies
[Federal Register Volume 81, Number 127 (Friday, July 1, 2016)]
[Notices]
[Pages 43201-43202]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-15703]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION
[OMB Control No. 9000-0136; Docket 2016-0053; Sequence 28]
Information Collection; Commercial Item Acquisitions
AGENCY: Department of Defense (DOD), General Services Administration
(GSA), and National Aeronautics and Space Administration (NASA).
ACTION: Notice of request for comments regarding an extension to an
existing OMB clearance.
-----------------------------------------------------------------------
SUMMARY: Under the provisions of the Paperwork Reduction Act, the
Regulatory Secretariat Division will be submitting to the Office of
Management and Budget (OMB) a request to review and approve an
extension of a previously approved information collection requirement
concerning the clauses and provisions required for use in commercial
item acquisitions.
DATES: Submit comments on or before August 30, 2016.
ADDRESSES: Submit comments identified by Information Collection 9000-
0136, Commercial Item Acquisitions, by any of the following methods:
Regulations.gov: https://www.regulations.gov.
Submit comments via the Federal eRulemaking portal by searching the
OMB control number. Select the link ``Submit a Comment'' that
corresponds with ``Information Collection 9000-0136, Commercial Item
Acquisitions''. Follow the instructions provided at the ``Submit a
Comment'' screen. Please include your name, company name (if any), and
``Information Collection 9000-0136, Commercial Item Acquisitions'' on
your attached document.
Mail: General Services Administration, Regulatory
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405.
ATTN: Ms. Flowers/IC 9000-0136, Commercial Item Acquisitions.
Instructions: Please submit comments only and cite Information
Collection 9000-0136, Commercial Item Acquisitions, in all
correspondence related to this collection. Comments received generally
will be posted without change to https://www.regulations.gov, including
any personal and/or business confidential information provided. To
confirm receipt of your comment(s), please check www.regulations.gov,
approximately two to three days after submission to verify posting
(except allow 30 days for posting of comments submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr. Michael O. Jackson, Procurement
Analyst, Office of Governmentwide Acquisition Policy, GSA, at 202-208-
4949, or email at michaelo.jackson@gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
The Federal Acquisition Streamlining Act of 1994 reformed Federal
acquisition statutes to encourage and facilitate the acquisition of
commercial items and services by the Federal Government. Accordingly,
DoD, NASA, and GSA amended the Federal Acquisition Regulation (FAR) to
include streamlined/simplified procedures for the acquisition of
commercial items.
Pertinent to this information collection, FAR Provision 52.212-3,
``Offeror Representations and Certifications--Commercial Items,'' was
implemented to combine the multitude of individual provisions used in
Government solicitations into a single provision for use in commercial
[[Page 43202]]
acquisitions. The provision is among the representations and
certifications that are available for completion in the System for
Award Management (SAM).
B. Annual Reporting Burden
Respondents: 397,000.
Responses per Respondent: 1.46.
Total Responses: 579,620.
Hours per Response: .500.
Total Burden Hours: 289,810.
Frequency: On Occasion.
Affected Public: Businesses or other for-profit and not-for-profit
institutions.
C. Public Comments
Public comments are particularly invited on: Whether this
collection of information is necessary for the proper performance of
functions of the Federal Acquisition Regulations (FAR), and whether it
will have practical utility; whether our estimate of the public burden
of this collection of information is accurate, and based on valid
assumptions and methodology; ways to enhance the quality, utility, and
clarity of the information to be collected; and ways in which we can
minimize the burden of the collection of information on those who are
to respond, through the use of appropriate technological collection
techniques or other forms of information technology.
Obtaining Copies of Proposals: Requesters may obtain a copy of the
information collection documents from the General Services
Administration, Regulatory Secretariat Division (MVCB), 1800 F Street
NW., Washington, DC 20405, telephone 202-501-4755.
Please cite OMB Control No. 9000-0136 regarding Commercial Item
Acquisitions in all correspondence.
Dated: June 28, 2016.
Mahruba Uddowla,
Acting Director, Federal Acquisition Policy Division, Office of
Governmentwide Acquisition Policy, Office of Acquisition Policy, Office
of Governmentwide Policy.
[FR Doc. 2016-15703 Filed 6-30-16; 8:45 am]
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