Advisory Committee on the Medical Uses of Isotopes; Renewal Notice, 13598-13599 [2010-6205]
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Federal Register / Vol. 75, No. 54 / Monday, March 22, 2010 / Notices
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[Notice (10–032)]
NASA Advisory Council; Meeting
National Aeronautics and
Space Administration.
ACTION: Notice of meeting.
AGENCY:
SUMMARY: In accordance with the
Federal Advisory Committee Act, Public
Law 92–463, as amended, the National
Aeronautics and Space Administration
announce a meeting for the Information
Technology Infrastructure Committee of
the NASA Advisory Council.
DATES: Thursday, April 15, 2010, 9
a.m.–5 p.m. (EST), and Friday, April 16,
2010, 11 a.m.–5 p.m.
Meet-Me-Number: 1–877–613–3958;
#2939943.
NASA Headquarters, 300 E
Street, SW., Washington, DC, Room
2O43
Ms. Tereda J. Frazier, Executive
Secretary, Information Technology
Infrastructure Committee, NASA
Advisory Council, at e-mail
tereda.j.frazier@nasa.gov or by
telephone at (202) 358–2595 by no later
than April 8, 2010. To expedite
admittance, attendees with U.S.
citizenship can provide identifying
information 3 working days in advance
by contacting Ms. Tereda J. Frazier via
e-mail at tereda.j.frazier@nasa.gov or by
telephone at 202–358–2595. Persons
with disabilities who require assistance
should indicate this.
Dated: March 16, 2010.
P. Diane Rausch,
Advisory Committee Management Officer,
National Aeronautics and Space
Administration.
[FR Doc. 2010–6293 Filed 3–19–10; 8:45 am]
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ADDRESSES:
Ms.
Tereda J. Frazier, Executive Secretary
for the Information Technology
Infrastructure Committee, National
Aeronautics and Space Administration
Headquarters, Washington, DC, 20546,
(202) 358–2595.
SUPPLEMENTARY INFORMATION: The topics
of discussion for the meeting are the
following:
• NASA IT Summit Briefing.
• NASA IT Infrastructure Briefing.
• Status of NASA Supercomputing.
• NASA IT Security Operations.
• ASCS Briefing.
• IT Committee Work Plan Actions/
Assignments.
• Logistics.
The meeting will be open to the
public up to the seating capacity of the
room. It is imperative that these
meetings be held on this date to
accommodate the scheduling priorities
of the key participants. Visitors will
need to show a valid picture
identification such as a driver’s license
to enter the NASA Headquarters
building (West Lobby—Visitors Control
Center), and must state that they are
attending the NASA Advisory Council
Information Technology Infrastructure
Committee meeting in room 2O43. All
non-U.S. citizens must fax copy of their
passport, and print or type their name,
current address, citizenship, company
affiliation (if applicable) to include
address, telephone number, and their
title, place of birth, date of birth, U.S.
visa information to include type,
number and expiration date, U.S. Social
Security Number (if applicable), and
place and date of entry into the U.S., to
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FOR FURTHER INFORMATION CONTACT:
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NEIGHBORHOOD REINVESTMENT
CORPORATION
Regular Board of Directors Meeting;
Sunshine Act
TIME AND DATE: 10 a.m., Monday, March
22, 2010.
PLACE: 1325 G Street, NW., Suite 800
Boardroom, Washington, DC 20005.
STATUS: Open.
CONTACT PERSON FOR MORE INFORMATION:
Erica Hall, Assistant Corporate
Secretary, (202) 220–2376;
ehall@nw.org.
Agenda
I. Call to Order
II. Approval of the Minutes
III. Summary Report of the Corporate
Administration Committee
IV. Approval of the Minutes
V. Summary Report of the Audit
Committee
VI. Approval of the Minutes
VII. Summary Report of the Finance,
Budget and Program Committee
VIII. Summary Report of the Corporate
Administration Committee
IX. Approval of Grants Exceeding One
Million Dollars
X. Financial Report
XI. Corporate Scorecard
XII. NHSA Update
XIII. Chief Executive Officer’s Quarterly
Management Report
XIV. Adjournment
Erica Hall,
Assistant Corporate Secretary.
[FR Doc. 2010–6154 Filed 3–19–10; 8:45 am]
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NUCLEAR REGULATORY
COMMISSION
Advisory Committee on the Medical
Uses of Isotopes; Renewal Notice
AGENCY: U.S. Nuclear Regulatory
Commission.
ACTION: This notice is to announce the
renewal of the Advisory Committee on
the Medical Uses of Isotopes (ACMUI)
for a period of two years.
The U. S.
Nuclear Regulatory Commission (NRC)
has determined that the renewal of the
charter for the Advisory Committee on
the Medical Uses of Isotopes for the two
year period commencing on March 16,
2010 is in the public interest, in
connection with duties imposed on the
Commission by law. This action is being
taken in accordance with the Federal
Advisory Committee Act, after
consultation with the Committee
Management Secretariat, General
Services Administration.
The purpose of the ACMUI is to
provide advice to NRC on policy and
technical issues that arise in regulating
the medical use of byproduct material
for diagnosis and therapy.
Responsibilities include providing
guidance and comments on current and
proposed NRC regulations and
regulatory guidance concerning medical
use; evaluating certain non-routine uses
of byproduct material for medical use;
and evaluating training and experience
of proposed authorized users. The
members are involved in preliminary
discussions of major issues in
determining the need for changes in
NRC policy and regulation to ensure the
continued safe use of byproduct
material. Each member provides
technical assistance in his/her specific
area(s) of expertise, particularly with
respect to emerging technologies.
Members also provide guidance as to
NRC’s role in relation to the
responsibilities of other Federal
agencies as well as of various
professional organizations and boards.
Members of this Committee have
demonstrated professional
qualifications and expertise in both
scientific and non-scientific disciplines
including nuclear medicine; nuclear
cardiology; radiation therapy; medical
physics; nuclear pharmacy; State
medical regulation; patient’s rights and
care; health care administration; and
Food and Drug Administration
regulation.
For further information please
contact: Ashley Cockerham, Office of
Federal and State Materials and
Environmental Management Programs,
SUPPLEMENTARY INFORMATION:
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Federal Register / Vol. 75, No. 54 / Monday, March 22, 2010 / Notices
U.S. Nuclear Regulatory Commission,
Washington, DC 20555; Telephone (240)
888–7129; e-mail
Ashley.Cockerham@nrc.gov
Dated: March 16, 2010.
Andrew L. Bates,
Federal Advisory Committee Management
Officer.
[FR Doc. 2010–6205 Filed 3–19–10; 8:45 am]
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NUCLEAR REGULATORY
COMMISSION
[NRC–2010–0114]
Draft Regulatory Guide: Issuance,
Availability
AGENCY: Nuclear Regulatory
Commission.
ACTION: Notice of issuance and
availability of Draft Regulatory Guide,
DG–8040, ‘‘Health Physics Surveys
During Enriched Uranium-235
Processing and Fuel Fabrication.’’
FOR FURTHER INFORMATION CONTACT:
Tyrone Naquin, U.S. Nuclear Regulatory
Commission, Washington, DC 20555–
0001, telephone: (301) 492–3187 or email Tyrone.Naquin@nrc.gov.
SUPPLEMENTARY INFORMATION:
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I. Introduction
The U.S. Nuclear Regulatory
Commission (NRC) is issuing for public
comment a draft guide in the agency’s
‘‘Regulatory Guide’’ series. This series
was developed to describe and make
available to the public such information
as methods that are acceptable to the
NRC staff for implementing specific
parts of the NRC’s regulations,
techniques that the staff uses in
evaluating specific problems or
postulated accidents, and data that the
staff needs in its review of applications
for permits and licenses.
The draft regulatory guide (DG) is
temporarily identified by its task
number, DG–8040, which should be
mentioned in all related
correspondence. DG–8040 is proposed
Revision 2 of Regulatory Guide 8.24,
dated October 1979. This guide specifies
the types and frequencies of surveys
that are acceptable to the staff of the
NRC for the protection of workers in
plants licensed by the NRC to process
enriched uranium and fabricate
uranium fuel.
Title 10, Section 20.1501(a), of the
Code of Federal Regulations (10 CFR
20.1501(a)) requires that each licensee
make or cause to be made such surveys
as may be necessary for it to comply
with the regulations in that part. As
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used in 10 CFR Part 20, ‘‘Standards for
Protection Against Radiation,’’ the term
‘‘survey’’ refers to an evaluation of the
radiation hazards incident to the
production, use, release, disposal, or
presence of radioactive materials or
other sources of radiation under a
specific set of conditions.
This guide does not relate to the
processing of uranium-233, nor does it
deal specifically with the following
aspects of an acceptable occupational
health physics program that are closely
related to surveys: (1) The number and
qualification of the health physics staff,
(2) instrumentation, including types,
numbers of instruments, limitations of
use, accuracy, and calibration, (3)
personnel dosimetry, and (4) bioassay.
Guidance on bioassay for uranium
appears in Regulatory Guide 8.11,
‘‘Applications of Bioassay for Uranium.’’
II. Further Information
The NRC staff is soliciting comments
on DG–8040. Comments may be
accompanied by relevant information or
supporting data and should mention
DG–8040 in the subject line. Comments
submitted in writing or in electronic
form will be made available to the
public in their entirety through the
NRC’s Agencywide Documents Access
and Management System (ADAMS).
Comments would be most helpful if
received by May 3, 2010. Comments
received after that date will be
considered if it is practical to do so, but
the NRC is able to ensure consideration
only for comments received on or before
this date. Although a time limit is given,
comments and suggestions in
connection with items for inclusion in
guides currently being developed or
improvements in all published guides
are encouraged at any time.
ADDRESSES: You may submit comments
by any one of the following methods.
Please include Docket ID NRC–2010–
0115 in the subject line of your
comments. Comments submitted in
writing or in electronic form will be
posted on the NRC Web site and on the
Federal rulemaking Web site
Regulations.gov. Because your
comments will not be edited to remove
any identifying or contact information,
the NRC cautions you against including
any information in your submission that
you do not want to be publicly
disclosed.
The NRC requests that any party
soliciting or aggregating comments
received from other persons for
submission to the NRC inform those
persons that the NRC will not edit their
comments to remove any identifying or
contact information, and therefore, they
should not include any information in
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13599
their comments that they do not want
publicly disclosed.
Federal Rulemaking Web site: Go to
https://www.regulations.gov and search
for documents filed under Docket ID
NRC–2010–0115. Address questions
about NRC dockets to Carol Gallagher
301–492–3668; e-mail
Carol.Gallagher@nrc.gov.
Mail comments to: Michael T. Lesar,
Chief, Rulemaking and Directives
Branch (RDB), Office of Administration,
Mail Stop: TWB–05–B01M, U.S.
Nuclear Regulatory Commission,
Washington, DC 20555–0001, or by fax
to RDB at (301) 492–3446.
You can access publicly available
documents related to this notice using
the following methods:
NRC’s Public Document Room (PDR):
The public may examine and have
copied for a fee publicly available
documents at the NRC’s PDR, Room O1
F21, One White Flint North, 11555
Rockville Pike, Rockville, Maryland.
NRC’s Agencywide Documents Access
and Management System (ADAMS):
Publicly available documents created or
received at the NRC are available
electronically at the NRC’s Electronic
Reading Room at https://www.nrc.gov/
reading-rm/adams.html. From this page,
the public can gain entry into ADAMS,
which provides text and image files of
NRC’s public documents. If you do not
have access to ADAMS or if there are
problems in accessing the documents
located in ADAMS, contact the NRC’s
PDR reference staff at 1–800–397–4209,
301–415–4737, or by e-mail to
pdr.resource@nrc.gov. DG–8040 is
available electronically under ADAMS
Accession Number ML092150040. In
addition, electronic copies of DG–8040
are available through the NRC’s public
Web site under Draft Regulatory Guides
in the ‘‘Regulatory Guides’’ collection of
the NRC’s Electronic Reading Room at
https://www.nrc.gov/reading-rm/doccollections/
Federal Rulemaking Web site: Public
comments and supporting materials
related to this notice can be found at
https://www.regulations.gov by searching
on Docket ID: NRC–2010–0115.
Regulatory guides are not
copyrighted, and Commission approval
is not required to reproduce them.
Dated at Rockville, Maryland, this 10th day
of March 2010.
For the Nuclear Regulatory Commission.
Andrea D. Valentin,
Chief, Regulatory Guide Development Branch,
Division of Engineering, Office of Nuclear
Regulatory Research.
[FR Doc. 2010–6196 Filed 3–19–10; 8:45 am]
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Agencies
[Federal Register Volume 75, Number 54 (Monday, March 22, 2010)]
[Notices]
[Pages 13598-13599]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-6205]
=======================================================================
-----------------------------------------------------------------------
NUCLEAR REGULATORY COMMISSION
Advisory Committee on the Medical Uses of Isotopes; Renewal
Notice
AGENCY: U.S. Nuclear Regulatory Commission.
ACTION: This notice is to announce the renewal of the Advisory
Committee on the Medical Uses of Isotopes (ACMUI) for a period of two
years.
-----------------------------------------------------------------------
SUPPLEMENTARY INFORMATION: The U. S. Nuclear Regulatory Commission
(NRC) has determined that the renewal of the charter for the Advisory
Committee on the Medical Uses of Isotopes for the two year period
commencing on March 16, 2010 is in the public interest, in connection
with duties imposed on the Commission by law. This action is being
taken in accordance with the Federal Advisory Committee Act, after
consultation with the Committee Management Secretariat, General
Services Administration.
The purpose of the ACMUI is to provide advice to NRC on policy and
technical issues that arise in regulating the medical use of byproduct
material for diagnosis and therapy. Responsibilities include providing
guidance and comments on current and proposed NRC regulations and
regulatory guidance concerning medical use; evaluating certain non-
routine uses of byproduct material for medical use; and evaluating
training and experience of proposed authorized users. The members are
involved in preliminary discussions of major issues in determining the
need for changes in NRC policy and regulation to ensure the continued
safe use of byproduct material. Each member provides technical
assistance in his/her specific area(s) of expertise, particularly with
respect to emerging technologies. Members also provide guidance as to
NRC's role in relation to the responsibilities of other Federal
agencies as well as of various professional organizations and boards.
Members of this Committee have demonstrated professional
qualifications and expertise in both scientific and non-scientific
disciplines including nuclear medicine; nuclear cardiology; radiation
therapy; medical physics; nuclear pharmacy; State medical regulation;
patient's rights and care; health care administration; and Food and
Drug Administration regulation.
For further information please contact: Ashley Cockerham, Office of
Federal and State Materials and Environmental Management Programs,
[[Page 13599]]
U.S. Nuclear Regulatory Commission, Washington, DC 20555; Telephone
(240) 888-7129; e-mail Ashley.Cockerham@nrc.gov
Dated: March 16, 2010.
Andrew L. Bates,
Federal Advisory Committee Management Officer.
[FR Doc. 2010-6205 Filed 3-19-10; 8:45 am]
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