Mine Safety and Health Research Advisory Committee: Notice of Charter Renewal, 78800-78801 [E8-30487]
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78800
Federal Register / Vol. 73, No. 247 / Tuesday, December 23, 2008 / Notices
foreign banks, and Edge and agreement
corporations.
Annual reporting hours: 59,902 hours.
Estimated average hours per response:
Initial terms disclosure, 1.5 minutes;
change in terms disclosure, 1 minute;
periodic disclosure, 7 hours; and error
resolution rules, 30 minutes.
Number of respondents: 1,205.
General description of report: This
information collection is mandatory (15
U.S.C. 1693 et seq.). The disclosures
required by the rule and information
about error allegations and their
resolution are confidential between the
institution and the consumer. Since the
Federal Reserve does not collect any
information, no issue of confidentiality
arises. However, the information, if
made available to the Federal Reserve,
may be protected from disclosure under
exemptions (b)(4), (6), and (8) of the
Freedom of Information Act (5 U.S.C.
552(b)(4), (6), and (8)).
Abstract: The Electronic Funds
Transfer Act and Regulation E are
designed to ensure adequate disclosure
of basic terms, costs, and rights relating
to electronic fund transfer (EFT)
services provided to consumers.
Institutions offering EFT services must
disclose to consumers certain
information, including: initial and
updated EFT terms, transaction
information, periodic statements of
activity, the consumer’s potential
liability for unauthorized transfers, and
error resolution rights and procedures.
EFT services include automated teller
machines, telephone bill payment;
point-of-sale transfers in retail stores,
fund transfers initiated through the
internet, and preauthorized transfers to
or from a consumer’s account.
Current Actions: On October 15, 2008,
the Federal Reserve published a notice
in the Federal Register (73 FR 61126)
requesting public comment for 60 days
on the extension, without revision, of
this information collection. The
comment period for this notice expired
on December 15, 2008. The Federal
Reserve did not receive any comments.
Board of Governors of the Federal Reserve
System, dated December 18, 2009.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E8–30493 Filed 12–22–08; 8:45 am]
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GENERAL SERVICES
ADMINISTRATION
[OMB Control No. 3090–0204]
General Services Administration
Acquisition Regulation; Information
Collection; Commercial Delivery
Schedule Clause and Notice of
Shipment
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 of 1995 (44
U.S.C. Chapter 35), the General Services
Administration will be submitting to the
Office of Management and Budget
(OMB) a request to review and approve
an extension of a currently approved
information collection requirement
regarding commercial delivery schedule
clause and notice of shipment. The
clearance currently expires on
December 31, 2008.
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:
February 23, 2009.
FOR FURTHER INFORMATION CONTACT:
Suzanne Neurauter, Procurement
Analyst, Contract Policy Division, at
telephone (202) 219–0310 or via e-mail
to suzanne.neurauter@gsa.gov.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to the Regulatory Secretariat
(VPR), General Services Administration,
Room 4041, 1800 F Street, NW.,
Washington, DC 20405. Please cite OMB
Control No. 3090–0204, Commercial
Delivery Schedule Clause and Notice of
Shipment, in all correspondence.
SUPPLEMENTARY INFORMATION:
A. Purpose
The Commercial Delivery Schedule
(Multiple Award Schedule) clause
required offerors to provide their
commercial delivery terms and
conditions. FSS awards contracts to
commercial firms under terms and
conditions that mirror commercial
practices for the supplies and services.
In order to ensure the Government
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obtains the supplies within the offeror’s
commercial delivery timeframe, the
offeror must provide the information
requested in the GSAR clause,
Commercial Delivery Schedule
(Multiple Award Schedule). Such a
notice is necessary when preparations
need to be made for docking
arrangements, storage, trans-shipment of
materials handling equipment of
supplies and equipment upon delivery,
labor and inside delivery at destination.
B. Annual Reporting Burden
Total Responses annually: 10,305.
Hours Per Response: .26.
Total Burden Hours: 2741.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat (VPR), 1800 F
Street, NW., Room 4041, Washington,
DC 20405, telephone (202) 501–4225.
Please cite OMB Control No. 3090–0204,
Commercial Delivery Schedule Clause
and Notice of Shipment, in all
correspondence.
Dated: December 18, 2008.
Al Matera,
Director, Office of Acquisition Policy.
[FR Doc. E8–30504 Filed 12–22–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Mine Safety and Health Research
Advisory Committee: Notice of Charter
Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the Mine
Safety and Health Research Advisory
Committee, Centers for Disease Control
and Prevention, Department of Health
and Human Services, has been renewed
for a 2-year period through November
30, 2010.
For information, contact Jeffrey
Kohler, Ph.D., Executive Secretary,
Mine Safety and Health Research
Advisory Committee, Centers for
Disease Control and Prevention,
Department of Health and Human
Services, 626 Cochrans Mill Road,
Mailstop P05, Pittsburgh, Pennsylvania
15236, Telephone (412) 386–5301 or fax
(412) 386–5300.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
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Federal Register / Vol. 73, No. 247 / Tuesday, December 23, 2008 / Notices
management activities, for both CDC
and the Agency for Toxic Substances
and Disease Registry.
Dated: December 15, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–30487 Filed 12–22–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors,
Coordinating Center for Health
Promotion (BSC, CCHP)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting of the
aforementioned committee:
Times and Dates: 1 p.m.–5 p.m., January
14, 2009; 8:30 a.m.–3:30 p.m., January 15,
2009.
Place: CDC, 1825 Century Boulevard, NE.,
Century Center Building 2400, Room 1042,
Atlanta, Georgia 30345.
Status: Open to the public, limited only by
the space available. The meeting room
accommodates approximately 75 people.
Purpose: This BSC is charged with
providing advice and guidance to the
Secretary of Health and Human Services, the
Director of CDC, and the Director of CCHP
concerning strategies and goals for the
programs and research within the National
Center on Birth Defects and Developmental
Disabilities and the National Center for
Chronic Disease Prevention and Health
Promotion.
Matters To Be Discussed: The agenda will
include an introduction to the federal
advisory committee process for new
members; an overview of the CDC, CCHP,
and the national centers; and a discussion of
the secondary review process.
Agenda items are subject to change as
priorities dictate.
Providing Oral or Written Comments: It is
the policy of the BSC, CCHP to accept written
public comments and provide a brief period
for oral public comments. Oral Comments: In
general, each individual or group requesting
to make an oral presentation will be limited
to a total time of five minutes (unless
otherwise indicated). Speakers must also
submit their comments in writing for
inclusion in the meeting’s Summary Report.
To ensure adequate time is scheduled for
public comments, individuals or groups
planning to make an oral presentation
should, when possible, notify the contact
person below at least one week prior to the
meeting date. Written Comments: For
individuals or groups unable to attend the
meeting, the CCHP BSC accepts written
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comments until the date of the meeting
(unless otherwise stated). However, the
comments should be received at least one
week prior to the meeting date so that the
comments may be made available to the BSC
for their consideration and public
distribution. Written comments, one hard
copy with original signature, should be
provided to the contact person below.
Written comments will be included in the
meeting’s Summary Report.
Contact Person for Additional Information:
Karen Steinberg, PhD, Senior Science Officer,
Coordinating Center for Health Promotion,
CDC, 4770 Buford Highway, NE., Mailstop E–
70, Atlanta, Georgia 30341; telephone (404)
498–6700; fax (404) 498–6880; or via e-mail
at Karen.Steinberg@cdc.hhs.gov.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register Notices
pertaining to announcements of meetings and
other committee management activities, for
CDC and the Agency for Toxic Substances
and Disease Registry.
Dated: December 12, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–30486 Filed 12–22–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Clinical Laboratory Improvement
Advisory Committee, (CLIAC)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting of the
aforementioned committee:
Times and Dates: 8:30 a.m.–5 p.m.,
February 4, 2009, 8:30 a.m.–3:30 p.m.,
February 5, 2009.
Place: CDC, 1600 Clifton Road, NE., Tom
Harkin Global Communications Center,
Building 19, Room 232, Auditorium B,
Atlanta, Georgia 30333.
Status: Open to the public, limited only by
the space available. The meeting room
accommodates approximately 100 people.
Purpose: This Committee is charged with
providing scientific and technical advice and
guidance to the Secretary of Health and
Human Services, the Assistant Secretary for
Health, and the Director, CDC, regarding the
need for, and the nature of, revisions to the
standards under which clinical laboratories
are regulated; the impact on medical and
laboratory practice of proposed revisions to
the standards; and the modification of the
standards to accommodate technological
advances.
Matters To Be Discussed: The agenda will
include updates from the CDC, the Centers
for Medicare & Medicaid Services, and the
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Food and Drug Administration; and
presentations and discussions addressing
studies and evaluation of laboratory practices
and standards.
Agenda items are subject to change as
priorities dictate.
New Information—Online Registration
Required: In order to expedite security
clearance process at the CDC Roybal Campus
located on Clifton Road, all CLIAC attendees
are required to register for the meeting online
at least 14 days in advance at https://
wwwn.cdc.gov/cliac/default.aspx by clicking
the ‘‘Register for a Meeting’’ link and
completing all forms according to the
instructions given. Please complete all the
required fields before submitting your
registration and submit no later than January
21, 2009.
Providing Oral or Written Comments: It is
the policy of CLIAC to accept written public
comments and provide a brief period for oral
public comments whenever possible. Oral
Comments: In general, each individual or
group requesting to make an oral
presentation will be limited to a total time of
five minutes (unless otherwise indicated).
Speakers must also submit their comments in
writing for inclusion in the meeting’s
Summary Report. To assure adequate time is
scheduled for public comments, individuals
or groups planning to make an oral
presentation should, when possible, notify
the contact person below at least one week
prior to the meeting date. Written Comments:
For individuals or groups unable to attend
the meeting, CLIAC accepts written
comments until the date of the meeting
(unless otherwise stated). However, the
comments should be received at least one
week prior to the meeting date so that the
comments may be made available to the
Committee for their consideration and public
distribution. Written comments, one hard
copy with original signature, should be
provided to the contact person below.
Written comments will be included in the
meeting’s Summary Report.
Contact Person for Additional Information:
Nancy Anderson, Chief, Laboratory Practice
Standards Branch, Division of Laboratory
Systems, National Center for Preparedness,
Detection, and Control of Infectious Diseases,
Coordinating Center for Infectious Diseases,
CDC, 1600 Clifton Road, NE., Mailstop F–11,
Atlanta, Georgia 30333; telephone (404) 498–
2741; fax (404) 498–2219; or via e-mail at
Nancy.Anderson@cdc.hhs.gov
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register Notices
pertaining to announcements of meetings and
other committee management activities, for
CDC and the Agency for Toxic Substances
and Disease Registry.
Dated: December 15, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–30485 Filed 12–22–08; 8:45 am]
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Agencies
[Federal Register Volume 73, Number 247 (Tuesday, December 23, 2008)]
[Notices]
[Pages 78800-78801]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-30487]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Mine Safety and Health Research Advisory Committee: Notice of
Charter Renewal
This gives notice under the Federal Advisory Committee Act (Pub. L.
92-463) of October 6, 1972, that the Mine Safety and Health Research
Advisory Committee, Centers for Disease Control and Prevention,
Department of Health and Human Services, has been renewed for a 2-year
period through November 30, 2010.
For information, contact Jeffrey Kohler, Ph.D., Executive
Secretary, Mine Safety and Health Research Advisory Committee, Centers
for Disease Control and Prevention, Department of Health and Human
Services, 626 Cochrans Mill Road, Mailstop P05, Pittsburgh,
Pennsylvania 15236, Telephone (412) 386-5301 or fax (412) 386-5300.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of meetings and other committee
[[Page 78801]]
management activities, for both CDC and the Agency for Toxic Substances
and Disease Registry.
Dated: December 15, 2008.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. E8-30487 Filed 12-22-08; 8:45 am]
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