Memorandum of Understanding Between the Food and Drug Administration and the Food and Drug Administration Alumni Association, 55910-55914 [05-19016]
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55910
Federal Register / Vol. 70, No. 184 / Friday, September 23, 2005 / Notices
(4) Increase information
dissemination and training, and
(5) Improve coordination across the
radiological health community.
II. Agenda
On October 31, 2005, FDA is
providing the opportunity for a number
of stakeholder organizations to discuss
how they can assist FDA in
implementing the program and in
addressing important public health
problems. FDA and its stakeholders will
discuss the following aspects of the
radiological health plan overview:
• Standards—Discussion will
consider the following topics: Increased
reliance by FDA on consensus radiation
safety performance standards, the role of
national and international standards,
and the role of State regulations in
assuring product safety and proper use.
• Monitoring the Use of Radiation—
Discussion will consider the following
topics: The shift of CDRH’s focus from
products to users, patients, and
consumers; adverse event reporting;
State program roles in ensuring
appropriate use of radiation; facility
quality assurance programs; and the
establishment of a voluntary patient
radiation dose reporting system for
diagnostic imaging procedures that use
ionizing radiation. This system could be
used to monitor national exposure
trends and provide a basis for
establishing diagnostic reference levels
of patient dose for use in facility quality
improvement programs.
• Monitoring the Industry—
Discussion will consider the following
topics: The shift of FDA emphasis from
testing products, to inspecting
manufacturers to assure quality
manufacturing and products; the
reduction of reporting requirements;
and the development of electronic
reporting methods.
• Education—Discussion will
consider education and training for
manufacturers, regulators, and users.
On November 1, 2005, FDA will hold
concurrent discussion sessions
throughout the day on the Standards,
Monitoring, and Education topics to
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provide further opportunity for
stakeholder comment and discussion.
FDA will provide an opportunity for
comment during the public comment
period for individuals and/or
organizations on October 31, 2005. In
addition, the agency will provide an
opportunity to present individual
viewpoints during the concurrent
discussion sessions on November 1,
2005. FDA reserves the right to limit the
time of speakers during the public
comment periods.
Dated: September 19, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–19077 Filed 9–20–05; 3:31 pm]
III. Registration
Participants must register for the
meeting by October 17, 2005.
Acceptance will be on a first-come, firstserved basis. There will be no onsite
registration and unregistered
participants will not be added to the
program. Please register online at https://
www.fda.gov/cdrh/meetings/
120303.html. Persons without Internet
access may register for the onsite
meeting by calling 301–594–3309 by
October 17, 2005.
If you need special accommodations
due to a disability, please fax
information regarding those needs to
Kaye Chesemore at 301–594–3306, at
least 7 days in advance of the meeting.
Memorandum of Understanding
Between the Food and Drug
Administration and the Food and Drug
Administration Alumni Association
IV. Request for Suggestions,
Recommendations, and Materials
FDA is particularly interested in
receiving suggestions from stakeholders
related to the topics listed previously in
this document. Send suggestions or
recommendations to the Division of
Dockets Management (see ADDRESSES).
FDA will place an additional copy of
any material it receives in the docket for
this document (2005N–0375).
Suggestions, recommendations, and
materials may be seen at the Division of
Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday (see
ADDRESSES).
V. Transcripts
Following the meeting, transcripts
will be available for review at the
Division of Dockets Management (see
ADDRESSES).
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BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FDA 225–04–8000]
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is providing
notice of a memorandum of
understanding (MOU) between FDA and
the Food and Drug Administration
Alumni Association, Inc. The purpose
of this MOU is to establish a greater
collaboration between FDA and the
Food and Drug Administration Alumni
Association, Inc., regarding FDAs 2006
Centennial Observance.
The agreement became effective
July 28, 2004.
DATES:
FOR FURTHER INFORMATION CONTACT:
Mary Hitch, Senior Advisor, Office of
External Relations (HF–10), 5600
Fishers Lane, Rockville, MD 20857,
301–827–4406.
In
accordance with 21 CFR 20.108(c),
which states that all written agreements
and MOUs between FDA and others
shall be published in the Federal
Register, the agency is publishing notice
of this MOU.
SUPPLEMENTARY INFORMATION:
Dated: September 8, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
BILLING CODE 4160–01–S
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55914
Federal Register / Vol. 70, No. 184 / Friday, September 23, 2005 / Notices
BILLING CODE 4160–01–C
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
[CFDA 93.223]
Cooperative Agreement for Border
Health Best Practices
Office of Rural Health Policy,
HRSA, DHHS.
ACTION: Notice of Single Source Award.
AGENCY:
VerDate Aug<31>2005
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SUMMARY: The Office of Rural Health
Policy (ORHP), in cooperation with the
Office of Global Health Affairs (OGHA),
Office of Minority Health (OMH), Office
on Women’s Health (OWH), and Centers
for Disease Control and Prevention
(CDC) will award a one year single
source award to the U.S.-Mexico Border
Health Association (USMBHA) to
identify and promote best practices in
border communities. As defined in the
La Paz Agreement, the border region is
100 km north and south of the
international boundary line between the
United States and Mexico. Funds will
be used on both sides of the U.S.Mexico border for the development of
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activities under the second annual
Border Binational Health Week (October
10–16, 2005).
FOR FURTHER INFORMATION CONTACT:
Elizabeth Rezai-zadeh, Office of Rural
Health Policy, Room 9A–55, 5600
Fishers Lane, Rockville, MD 20857.
Telephone: 301–443–4107. E-mail:
erezai@hrsa.gov.
SUPPLEMENTARY INFORMATION:
Intended Recipient of the Award
U.S.-Mexico Border Health
Association in El Paso, TX.
Amount of the Award
$383,000.
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[FR Doc. 05–19016 Filed 9–22–05; 8:45 am]
Agencies
[Federal Register Volume 70, Number 184 (Friday, September 23, 2005)]
[Notices]
[Pages 55910-55914]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-19016]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[FDA 225-04-8000]
Memorandum of Understanding Between the Food and Drug
Administration and the Food and Drug Administration Alumni Association
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is providing notice of
a memorandum of understanding (MOU) between FDA and the Food and Drug
Administration Alumni Association, Inc. The purpose of this MOU is to
establish a greater collaboration between FDA and the Food and Drug
Administration Alumni Association, Inc., regarding FDAs 2006 Centennial
Observance.
DATES: The agreement became effective July 28, 2004.
FOR FURTHER INFORMATION CONTACT: Mary Hitch, Senior Advisor, Office of
External Relations (HF-10), 5600 Fishers Lane, Rockville, MD 20857,
301-827-4406.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 20.108(c), which
states that all written agreements and MOUs between FDA and others
shall be published in the Federal Register, the agency is publishing
notice of this MOU.
Dated: September 8, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
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[FR Doc. 05-19016 Filed 9-22-05; 8:45 am]
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