Submission for OMB Review; Ombudsman Inquiry/Request Instrument, 41962-41963 [2017-18675]
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41962
Federal Register / Vol. 82, No. 170 / Tuesday, September 5, 2017 / Notices
providing SF 1444, Request for
Authorization of Additional
Classification and Rate, for the
contractor and the Government to enter
the recordkeeping and information
collection data required by 29 CFR
5.5(a)(1)(ii) prior to transmitting the data
to the Department of Labor.
B. Annual Reporting Burden
Number of Respondents: 3,831.
Responses per Respondent: 2.
Total Annual Responses: 7,662.
Review time per response: 0.5.
Total Burden Hours: 3,831.
Dated: August 29, 2017.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Government-wide Acquisition
Policy, Office of Acquisition Policy, Office
of Government-wide Policy.
[FR Doc. 2017–18676 Filed 9–1–17; 8:45 am]
BILLING CODE 6820–EP–P
GENERAL SERVICES
ADMINISTRATION
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[OMB Control No. 3090–XXXX; Docket No.
2017–0001; Sequence 3]
Submission for OMB Review;
Ombudsman Inquiry/Request
Instrument
Office of Acquisition Policy,
Office of the Procurement Ombudsman
(OPO), General Services Administration
(GSA).
ACTION: Notice of request for comments
regarding a new request for an Office of
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17:43 Sep 01, 2017
Jkt 241001
Under the provisions of the
Paperwork Reduction Act, the
Regulatory Secretariat Division will be
submitting to the OMB a request to
review and approve a new information
collection requirement regarding OMB
Control No: 3090–XXXX; Ombudsman
Inquiry/Request Instrument. A notice
was published in the Federal Register
on May 19, 2017. No comments were
received.
SUMMARY:
Submit comments on or before
October 5, 2017.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to: Office of Information and
Regulatory Affairs of OMB, Attention:
Desk Officer for GSA, Room 10236,
NEOB, Washington, DC 20503.
Additionally submit a copy to GSA by
any of the following methods:
• Regulations.gov: https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching for ‘‘Information Collection
3090–XXXX; Ombudsman Inquiry/
Request Instrument.’’ Select the link
‘‘Submit a Comment’’ that corresponds
with ‘‘Information Collection 3090–
XXXX; Inquiry/Request Instrument.’’
Follow the instructions provided at the
‘‘Submit a Comment’’ screen. Please
include your name, company name (if
any), and ‘‘Information Collection 3090–
XXXX; Ombudsman Inquiry/Request
Instrument’’ on your attached
document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), 1800 F Street NW.,
Washington, DC 20405. ATTN: Ms.
Sosa/IC 3090–XXXX; Office of the
Ombudsman Inquiry/Request
Instrument.
Instructions: Please submit comments
only and cite Information Collection
3090–XXXX; Inquiry/Request
Instrument, 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: Ms.
Millisa Gary, GSA Procurement/Task &
Delivery Order Ombudsman, Office of
DATES:
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the 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:
Requester may obtain a copy of the
justification 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.
9000–0089, Request for Authorization of
Additional Classification and Rate, SF
1444, in all correspondence.
AGENCY:
Management and Budget (OMB)
clearance.
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Acquisition Policy, Office of the
Ombudsman, GSA, at telephone 202–
501–0699 or via email to millisa.gary@
gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
OPO wants to place an online intake
Instrument on the GSA Ombudsman’s
Web page for receiving inquiries from
vendors who are currently doing
business with, or interested in doing
business with GSA. The inquiries will
be collected by the GSA Ombudsman
and routed to the appropriate office for
resolution and/or implementation in the
case of recommendations for process or
program improvements. Reporting of the
data collected will help highlight
thematic issues that vendors encounter
with GSA acquisition programs,
processes or policies, and identify areas
where training is needed. The
information collected will also assist in
identifying and analyzing patterns and
trends to help improve efficiencies and
lead to improvements in current
practices.
B. Annual Reporting Burden
Maximum Potential Respondents:
118.
Responses per Respondent: 1.
Total Maximum Potential Annual
Responses: 118.
Hours per Response: .25.
Total Burden Hours: 29.5.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary, 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.
E:\FR\FM\05SEN1.SGM
05SEN1
Federal Register / Vol. 82, No. 170 / Tuesday, September 5, 2017 / Notices
Please cite OMB Control No. 3090–
XXXX, Inquiry/Request Instrument, in
all correspondence.
Jeffrey A. Koses,
Director, Office of Acquisition Policy, Office
of Government-wide Policy.
[FR Doc. 2017–18675 Filed 9–1–17; 8:45 am]
BILLING CODE 6820–61–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Patient Safety Organizations:
Voluntary Relinquishment From the
Quantros Patient Safety Center
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
ACTION: Notice of delisting.
AGENCY:
The Patient Safety Rule
authorizes AHRQ, on behalf of the
Secretary of HHS, to list as a PSO an
entity that attests that it meets the
statutory and regulatory requirements
for listing. A PSO can be ‘‘delisted’’ by
the Secretary if it is found to no longer
meet the requirements of the Patient
Safety Act and Patient Safety Rule,
when a PSO chooses to voluntarily
relinquish its status as a PSO for any
reason, or when a PSO’s listing expires.
AHRQ has accepted a notification of
voluntary relinquishment from the
Quantros Patient Safety Center of its
status as a PSO, and has delisted the
PSO accordingly.
DATES: The directories for both listed
and delisted PSOs are ongoing and
reviewed weekly by AHRQ. The
delisting was applicable at 12:00
Midnight ET (2400) on August 15, 2017.
ADDRESSES: Both directories can be
accessed electronically at the following
HHS Web site: https://
www.pso.ahrq.gov/listed.
FOR FURTHER INFORMATION CONTACT:
Eileen Hogan, Center for Quality
Improvement and Patient Safety, AHRQ,
5600 Fishers Lane, Room 06N94B,
Rockville, MD 20857; Telephone (toll
free): (866) 403–3697; Telephone (local):
(301) 427–1111; TTY (toll free): (866)
438–7231; TTY (local): (301) 427–1130;
Email: pso@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
Background
The Patient Safety and Quality
Improvement Act of 2005, 42 U.S.C.
299b–21 to b–26, (Patient Safety Act)
and the related Patient Safety and
Quality Improvement Final Rule, 42
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17:43 Sep 01, 2017
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CFR part 3 (Patient Safety Rule),
published in the Federal Register on
November 21, 2008, 73 FR 70732–
70814, establish a framework by which
hospitals, doctors, and other health care
providers may voluntarily report
information to Patient Safety
Organizations (PSOs), on a privileged
and confidential basis, for the
aggregation and analysis of patient
safety events.
The Patient Safety Act authorizes the
listing of PSOs, which are entities or
component organizations whose
mission and primary activity are to
conduct activities to improve patient
safety and the quality of health care
delivery.
HHS issued the Patient Safety Rule to
implement the Patient Safety Act.
AHRQ administers the provisions of the
Patient Safety Act and Patient Safety
Rule relating to the listing and operation
of PSOs. The Patient Safety Rule
authorizes AHRQ to list as a PSO an
entity that attests that it meets the
statutory and regulatory requirements
for listing. A PSO can be ‘‘delisted’’ if
it is found to no longer meet the
requirements of the Patient Safety Act
and Patient Safety Rule, when a PSO
chooses to voluntarily relinquish its
status as a PSO for any reason, or when
a PSO’s listing expires. Section 3.108(d)
of the Patient Safety Rule requires
AHRQ to provide public notice when it
removes an organization from the list of
federally approved PSOs.
AHRQ has accepted a notification
from the Quantros Patient Safety Center,
a component entity of Quantros Inc.,
PSO number P0014, to voluntarily
relinquish its status as a PSO.
Accordingly, the Quantros Patient
Safety Center was delisted effective at
12:00 Midnight ET (2400) on August 15,
2017.
The Quantros Patient Safety Center
has patient safety work product (PSWP)
in its possession. The PSO will meet the
requirements of section 3.108(c)(2)(i) of
the Patient Safety Rule regarding
notification to providers that have
reported to the PSO and of section
3.108(c)(2)(ii) regarding disposition of
PSWP consistent with section
3.108(b)(3). According to section
3.108(b)(3) of the Patient Safety Rule,
the PSO has 90 days from the effective
date of delisting and revocation to
complete the disposition of PSWP that
is currently in the PSO’s possession.
More information on PSOs can be
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obtained through AHRQ’s PSO Web site
at https://www.pso.ahrq.gov.
Sharon B. Arnold,
Deputy Director.
[FR Doc. 2017–18707 Filed 9–1–17; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0765; Docket No. CDC–2017–
0062]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to comment on proposed and/
or continuing information collections,
as required by the Paperwork Reduction
Act of 1995. This notice invites
comments on a request for an extension
of an approved information collection
entitled, CDC’s Fellowship Management
System. CDC uses the information
collected for processes that aid and
enhance the selection of fellowship
participants and host sites and to track
participant information that helps
strengthen the current, emerging, and
ever-changing public health workforce.
DATES: Written comments must be
received on or before November 6, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0062 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
SUMMARY:
E:\FR\FM\05SEN1.SGM
05SEN1
Agencies
[Federal Register Volume 82, Number 170 (Tuesday, September 5, 2017)]
[Notices]
[Pages 41962-41963]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-18675]
-----------------------------------------------------------------------
GENERAL SERVICES ADMINISTRATION
[OMB Control No. 3090-XXXX; Docket No. 2017-0001; Sequence 3]
Submission for OMB Review; Ombudsman Inquiry/Request Instrument
AGENCY: Office of Acquisition Policy, Office of the Procurement
Ombudsman (OPO), General Services Administration (GSA).
ACTION: Notice of request for comments regarding a new request for an
Office of Management and Budget (OMB) clearance.
-----------------------------------------------------------------------
SUMMARY: Under the provisions of the Paperwork Reduction Act, the
Regulatory Secretariat Division will be submitting to the OMB a request
to review and approve a new information collection requirement
regarding OMB Control No: 3090-XXXX; Ombudsman Inquiry/Request
Instrument. A notice was published in the Federal Register on May 19,
2017. No comments were received.
DATES: Submit comments on or before October 5, 2017.
ADDRESSES: Submit comments regarding this burden estimate or any other
aspect of this collection of information, including suggestions for
reducing this burden to: Office of Information and Regulatory Affairs
of OMB, Attention: Desk Officer for GSA, Room 10236, NEOB, Washington,
DC 20503. Additionally submit a copy to GSA by any of the following
methods:
Regulations.gov: https://www.regulations.gov. Submit
comments via the Federal eRulemaking portal by searching for
``Information Collection 3090-XXXX; Ombudsman Inquiry/Request
Instrument.'' Select the link ``Submit a Comment'' that corresponds
with ``Information Collection 3090-XXXX; Inquiry/Request Instrument.''
Follow the instructions provided at the ``Submit a Comment'' screen.
Please include your name, company name (if any), and ``Information
Collection 3090-XXXX; Ombudsman Inquiry/Request Instrument'' on your
attached document.
Mail: General Services Administration, Regulatory
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405.
ATTN: Ms. Sosa/IC 3090-XXXX; Office of the Ombudsman Inquiry/Request
Instrument.
Instructions: Please submit comments only and cite Information
Collection 3090-XXXX; Inquiry/Request Instrument, 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: Ms. Millisa Gary, GSA Procurement/Task
& Delivery Order Ombudsman, Office of Acquisition Policy, Office of the
Ombudsman, GSA, at telephone 202-501-0699 or via email to
millisa.gary@gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
OPO wants to place an online intake Instrument on the GSA
Ombudsman's Web page for receiving inquiries from vendors who are
currently doing business with, or interested in doing business with
GSA. The inquiries will be collected by the GSA Ombudsman and routed to
the appropriate office for resolution and/or implementation in the case
of recommendations for process or program improvements. Reporting of
the data collected will help highlight thematic issues that vendors
encounter with GSA acquisition programs, processes or policies, and
identify areas where training is needed. The information collected will
also assist in identifying and analyzing patterns and trends to help
improve efficiencies and lead to improvements in current practices.
B. Annual Reporting Burden
Maximum Potential Respondents: 118.
Responses per Respondent: 1.
Total Maximum Potential Annual Responses: 118.
Hours per Response: .25.
Total Burden Hours: 29.5.
C. Public Comments
Public comments are particularly invited on: Whether this
collection of information is necessary, 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.
[[Page 41963]]
Please cite OMB Control No. 3090-XXXX, Inquiry/Request Instrument,
in all correspondence.
Jeffrey A. Koses,
Director, Office of Acquisition Policy, Office of Government-wide
Policy.
[FR Doc. 2017-18675 Filed 9-1-17; 8:45 am]
BILLING CODE 6820-61-P