General Services Administration Acquisition Regulation; Information Collection; Sealed Bidding, 21743-21744 [2011-9264]
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erowe on DSK5CLS3C1PROD with NOTICES
Federal Register / Vol. 76, No. 74 / Monday, April 18, 2011 / Notices
comment and reply comment deadlines
by 60 days is in the public interest.
Extending the comment period will
ensure that parties have sufficient time
to consider and address developments
in this matter and the extent to which
they moot the controversy at issue in the
Petition. Therefore, interested parties
will now have until June 10, 2011 to file
comments and July 11, 2011 to file reply
comments as opposed to the April 11,
2011 and May 11, 2011 deadlines set
forth in the Public Notice.
Pursuant to §§ 1.415 and 1.419 of the
Commission’s rules, 47 CFR 1.415,
1.419, interested parties may file
comments and reply comments on or
before the dates indicated above.
Comments may be filed using: (1) The
Commission’s Electronic Comment
Filing System (ECFS), (2) the Federal
Government’s eRulemaking Portal, or
(3) by filing paper copies. See Electronic
Filing of Documents in Rulemaking
Proceedings, 63 FR 24121 (1998).
• Electronic Filers: Comments may be
filed electronically using the Internet by
accessing the ECFS: https://
fjallfoss.fcc.gov/ecfs2/ or the Federal
eRulemaking Portal: https://
www.regulations.gov.
• Paper Filers: Parties who choose to
file by paper must file an original and
four copies of each filing. If more than
one docket or rulemaking number
appears in the caption of this
proceeding, filers must submit two
additional copies for each additional
docket or rulemaking number.
Filings can be sent by hand or
messenger delivery, by commercial
overnight courier, or by first-class or
overnight U.S. Postal Service mail
(although we continue to experience
delays in receiving U.S. Postal Service
mail). All filings must be addressed to
the Commission’s Secretary, Office of
the Secretary, Federal Communications
Commission.
• All hand-delivered or messengerdelivered paper filings for the
Commission’s Secretary must be
delivered to FCC Headquarters at 445
12th St., SW., Room TW–A325,
Washington, DC 20554. The filing hours
are 8 a.m. to 7 p.m. All hand deliveries
must be held together with rubber bands
or fasteners. Any envelopes must be
disposed of before entering the building.
• Commercial overnight mail (other
than U.S. Postal Service Express Mail
and Priority Mail) must be sent to 9300
East Hampton Drive, Capitol Heights,
MD 20743.
• U.S. Postal Service first-class,
Express, and Priority mail must be
addressed to 445 12th Street, SW.,
Washington DC 20554.
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People with Disabilities: To request
materials in accessible formats for
people with disabilities (braille, large
print, electronic files, audio format),
send an e-mail to fcc504@fcc.gov or call
the Consumer & Governmental Affairs
Bureau at 202–418–0530 (voice), 202–
418–0432 (tty).
Federal Communications Commission.
Nese Guendelsberger,
Chief, Spectrum and Competition Policy
Division, Wireless Telecommunications
Bureau.
[FR Doc. 2011–9199 Filed 4–15–11; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL MARITIME COMMISSION
[Docket No. 11–06]
Indigo Logistics, LLC, Liliya Ivanenko,
and Leonid Ivanenko—Possible
Violations of Section 19 of the
Shipping Act of 1984 and the
Commission’s Regulations; Order of
Investigation and Hearing
AGENCY:
Federal Maritime Commission.
Notice of Order of Investigation
and Hearing.
ACTION:
Authority: 46 U.S.C. 41302.
The Order of Investigation and
Hearing was served April 7, 2011.
DATES:
On April
7, 2011 the Federal Maritime
Commission instituted an Order of
Investigation and Hearing entitled
Indigo Logistics, LLC; Liliya Ivanenko;
and Leonid Ivanenko—Possible
Violations of Section 19 of the Shipping
Act of 1984 and the Commission’s
Regulations at 46 CFR part 515. Acting
pursuant to Section 11 of the Shipping
Act, 46 U.S.C. 41302, that investigation
is instituted to determine:
(1) Whether Indigo Logistics, LLC,
Liliya Ivanenko, and Leonid Ivanenko
violated Section 19 of the Shipping Act,
46 U.S.C. 40901, 40902, and the
Commission’s regulations at 46 CFR part
515, by acting as an ocean freight
forwarder without a license or evidence
of financial responsibility;
(2) Whether, in the event violations of
Section 19 of the Shipping Act of 1984
are found, civil penalties should be
assessed against Indigo Logistics, LLC,
Liliya Ivanenko, and/or Leonid
Ivanenko, and, if so, the amount of
penalties to be assessed; and
(3) Whether, in the event violations
are found, appropriate cease and desist
orders should be issued.
SUPPLEMENTARY INFORMATION:
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21743
The Order may be viewed in its
entirety at https://www.fmc.gov.
Karen V. Gregory,
Secretary.
[FR Doc. 2011–9282 Filed 4–15–11; 8:45 am]
BILLING CODE 6730–01–P
GENERAL SERVICES
ADMINISTRATION
[OMB Control No. 3090–0200; Docket 2011–
0001; Sequence 1]
General Services Administration
Acquisition Regulation; Information
Collection; Sealed Bidding
Office of the Chief Acquisition
Officer, GSA.
ACTION: Notice of request for comments
regarding a renewal to an existing OMB
clearance.
AGENCY:
Under the provisions of the
Paperwork Reduction Act (44 U.S.C.
chapter 35), the Regulatory Secretariat
(MVCB) 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
regarding sealed bidding.
Public comments are particularly
invited on: Whether this collection of
information is necessary 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; and ways to enhance the
quality, utility, and clarity of the
information to be collected.
DATES: Submit comments on or before:
June 17, 2011.
FOR FURTHER INFORMATION CONTACT:
Michael O. Jackson, Procurement
Analyst, Contract Policy Branch, at
telephone (202) 208–4949 or
michaelo.jackson@gsa.gov.
SUMMARY:
Submit comments
identified by Information Collection
3090–0200 by any of the following
methods:
• Regulations.gov: https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
inputting ‘‘Information Collection 3090–
0200’’ under the heading ‘‘Enter
Keyword or ID’’ and selecting ‘‘Search’’.
Select the link ‘‘Submit a Comment’’ that
corresponds with ‘‘Information
Collection 3090–0200’’. Follow the
instructions provided at the ‘‘Submit a
Comment’’ screen. Please include your
name, company name (if any), and
‘‘Information Collection 3090–0200’’ on
your attached document.
ADDRESSES:
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21744
Federal Register / Vol. 76, No. 74 / Monday, April 18, 2011 / Notices
• Fax: 202–501–4067.
• Mail: General Services
Administration, Regulatory Secretariat
(MVCB), 1275 First Street, NE.,
Washington, DC 20417. Attn: Hada
Flowers/IC 3090–0200.
Instructions: Please submit comments
only and cite Information Collection
3090–0200, in all correspondence
related to this collection. All comments
received will be posted without change
to https://www.regulations.gov, including
any personal and/or business
confidential information provided.
SUPPLEMENTARY INFORMATION:
A. Purpose
The General Services Administration
is requesting that the Office of
Management and Budget (OMB) review
and approve information collection,
3090–0200, Sealed Bidding. The
information requested regarding an
offeror’s monthly production capability
is needed to make progressive awards to
ensure coverage of stock items.
B. Annual Reporting Burden
Respondents: 10.
Responses per Respondent: 1.
Hours per Response: .5.
Total Burden Hours: 5.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat (MVCB), 1275
First Street, NE., Washington, DC 20417,
telephone (202) 501–4755. Please cite
OMB Control No. 3090–0200, Sealed
Bidding, in all correspondence.
Dated: April 11, 2011.
Millisa Gary,
Acting Director, Office of Governmentwide
Acquisition Policy.
[FR Doc. 2011–9264 Filed 4–15–11; 8:45 am]
BILLING CODE 6820–61–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
erowe on DSK5CLS3C1PROD with NOTICES
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project: ‘‘Patient
SUMMARY:
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Safety Organization Certification for
Initial Listing and Related Forms,
Patient Safety Confidentiality Complaint
Form, and Common Formats. In
accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3521,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by June 17, 2011.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection plans,
data collection instruments, and specific
details on the estimated burden can be
obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at dorislefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Patient Safety Organization Certification
for Initial Listing and Related Forms,
Patient Safety Confidentiality Complaint
Form, and Common Formats
The Patient Safety and Quality
Improvement Act of 2005 (hereafter the
Patient Safety Act), 42 U.S.C. 299b–21
to 299b–26, was enacted in response to
growing concern about patient safety in
the United States and the Institute of
Medicine’s 1999 report, To Err is
Human: Building a Safer Health System.
The goal of the statute is to improve
patient safety by providing an incentive
for health care providers to work
voluntarily with experts in patient
safety to reduce risks and hazards to the
safety and quality of patient care. The
Patient Safety Act signifies the Federal
Government’s commitment to fostering
a culture of patient safety among health
care providers; it offers a mechanism for
creating an environment in which the
causes of risks and hazards to patient
safety can be thoroughly and honestly
examined and discussed without fear of
penalties and liabilities. It provides for
the voluntary formation of Patient
Safety Organizations (PSOs) that can
collect, aggregate, and analyze
confidential information reported
voluntarily by health care providers. By
analyzing substantial amounts of patient
safety event information across multiple
institutions, PSOs will be able to
identify patterns of failures and propose
measures to eliminate or reduce patient
safety risks and hazards.
In order to implement the Patient
Safety Act, the Department of Health
and Human Services (HHS) issued the
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Patient Safety and Quality Improvement
Final Rule (hereafter the Patient Safety
Rule), 42 CFR part 3, which became
effective on January 19, 2009. The
Patient Safety Rule establishes a
framework by which hospitals, doctors,
and other health care providers may
voluntarily report information to PSOs,
on a privileged and confidential basis,
for the aggregation and analysis of
patient safety events. In addition, the
Patient Safety Rule outlines the
requirements that entities must meet to
become PSOs and the process by which
the Secretary of HHS (hereafter the
Secretary) will review and accept
certifications and list PSOs.
In addition to the Patient Safety Act
and the Patient Safety Rule, HHS issued
Guidance Regarding Patient Safety
Organizations’ Reporting Obligations
and the Patient Safety and Quality
Improvement Act of 2005 (hereafter
Guidance) on December 30, 2010. The
Guidance addresses questions that have
arisen regarding the obligations of PSOs
where they or the organization of which
they are a part are legally obligated
under the Federal Food, Drug, and
Cosmetic Act (FDCA) and its
implementing regulations to report
certain information to the Food and
Drug Administration (FDA) and to
provide FDA with access to its records,
including access during an inspection of
its facilities. This Guidance applies to
all entities that seek to be or are PSOs
or component PSOs that have
mandatory FDA-reporting obligations
under the FDCA and its implementing
regulations (‘‘FDA-regulated reporting
entities’’) or are organizationally related
to such FDA-regulated reporting entities
(e.g., parent organizations, subsidiaries,
sibling organizations).
When PSOs meet the requirements of
the Patient Safety Act, the information
collected and the analyses and
deliberations regarding the information
receive Federal confidentiality and
privilege protections under this
legislation. The Secretary delegated
authority to the Director of the Office for
Civil Rights (OCR) to enforce the
confidentiality protections of the Patient
Safety Act. 71 Federal Register 28701–
28702 (May 17, 2006). OCR is
responsible for enforcing protections
regarding patient safety work product
(PSWP), which generally includes
information that could improve patient
safety, health care quality, or health care
outcomes and (1) is assembled or
developed by a provider for reporting to
a PSO and is reported to a PSO or (2)
is developed by a PSO for the conduct
of patient safety activities. Civil money
penalties may be imposed for knowing
or reckless impermissible disclosures of
E:\FR\FM\18APN1.SGM
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Agencies
[Federal Register Volume 76, Number 74 (Monday, April 18, 2011)]
[Notices]
[Pages 21743-21744]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-9264]
=======================================================================
-----------------------------------------------------------------------
GENERAL SERVICES ADMINISTRATION
[OMB Control No. 3090-0200; Docket 2011-0001; Sequence 1]
General Services Administration Acquisition Regulation;
Information Collection; Sealed Bidding
AGENCY: Office of the Chief Acquisition Officer, GSA.
ACTION: Notice of request for comments regarding a renewal to an
existing OMB clearance.
-----------------------------------------------------------------------
SUMMARY: Under the provisions of the Paperwork Reduction Act (44 U.S.C.
chapter 35), the Regulatory Secretariat (MVCB) 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 regarding sealed bidding.
Public comments are particularly invited on: Whether this
collection of information is necessary 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; and ways to enhance the quality, utility, and clarity
of the information to be collected.
DATES: Submit comments on or before: June 17, 2011.
FOR FURTHER INFORMATION CONTACT: Michael O. Jackson, Procurement
Analyst, Contract Policy Branch, at telephone (202) 208-4949 or
michaelo.jackson@gsa.gov.
ADDRESSES: Submit comments identified by Information Collection 3090-
0200 by any of the following methods:
Regulations.gov: https://www.regulations.gov. Submit
comments via the Federal eRulemaking portal by inputting ``Information
Collection 3090-0200'' under the heading ``Enter Keyword or ID'' and
selecting ``Search''. Select the link ``Submit a Comment'' that
corresponds with ``Information Collection 3090-0200''. Follow the
instructions provided at the ``Submit a Comment'' screen. Please
include your name, company name (if any), and ``Information Collection
3090-0200'' on your attached document.
[[Page 21744]]
Fax: 202-501-4067.
Mail: General Services Administration, Regulatory
Secretariat (MVCB), 1275 First Street, NE., Washington, DC 20417. Attn:
Hada Flowers/IC 3090-0200.
Instructions: Please submit comments only and cite Information
Collection 3090-0200, in all correspondence related to this collection.
All comments received will be posted without change to https://www.regulations.gov, including any personal and/or business
confidential information provided.
SUPPLEMENTARY INFORMATION:
A. Purpose
The General Services Administration is requesting that the Office
of Management and Budget (OMB) review and approve information
collection, 3090-0200, Sealed Bidding. The information requested
regarding an offeror's monthly production capability is needed to make
progressive awards to ensure coverage of stock items.
B. Annual Reporting Burden
Respondents: 10.
Responses per Respondent: 1.
Hours per Response: .5.
Total Burden Hours: 5.
Obtaining Copies of Proposals: Requesters may obtain a copy of the
information collection documents from the General Services
Administration, Regulatory Secretariat (MVCB), 1275 First Street, NE.,
Washington, DC 20417, telephone (202) 501-4755. Please cite OMB Control
No. 3090-0200, Sealed Bidding, in all correspondence.
Dated: April 11, 2011.
Millisa Gary,
Acting Director, Office of Governmentwide Acquisition Policy.
[FR Doc. 2011-9264 Filed 4-15-11; 8:45 am]
BILLING CODE 6820-61-P