Notice: Meetings: Food and Drug Administration and FDA Alumni Association

55910 Federal Register / Vol. 70, No.
184 / Friday, September 23, 2005 / Notices
(4) Increase information provide further opportunity for Dated: September 19, 2005.
dissemination and training, and stakeholder comment and discussion. Jeffrey Shuren,
(5) Improve coordination across the FDA will provide an opportunity for Assistant Commissioner for Policy.
radiological health community. comment during the public comment [FR Doc. 05–19077 Filed 9–20–05; 3:31 pm]
period for individuals and/or
II. Agenda BILLING CODE 4160–01–S
organizations on October 31, 2005. In
On October 31, 2005, FDA is addition, the agency will provide an
providing the opportunity for a number opportunity to present individual DEPARTMENT OF HEALTH AND
of stakeholder organizations to discuss viewpoints during the concurrent HUMAN SERVICES
how they can assist FDA in discussion sessions on November 1,
implementing the program and in 2005. FDA reserves the right to limit the Food and Drug Administration
addressing important public health time of speakers during the public
problems. FDA and its stakeholders will comment periods. [FDA 225–04–8000]
discuss the following aspects of the
radiological health plan overview: III. Registration Memorandum of Understanding
• Standards—Discussion will Participants must register for the Between the Food and Drug
consider the following topics: Increased meeting by October 17, 2005. Administration and the Food and Drug
reliance by FDA on consensus radiation Acceptance will be on a first-come, first- Administration Alumni Association
safety performance standards, the role of served basis. There will be no onsite
national and international standards, registration and unregistered AGENCY: Food and Drug Administration,
and the role of State regulations in participants will not be added to the HHS.
assuring product safety and proper use. program. Please register online at http://
• Monitoring the Use of Radiation— ACTION: Notice.
www.fda.gov/cdrh/meetings/
Discussion will consider the following 120303.html. Persons without Internet
topics: The shift of CDRH’s focus from SUMMARY: The Food and Drug
access may register for the onsite
products to users, patients, and Administration (FDA) is providing
meeting by calling 301–594–3309 by
consumers; adverse event reporting; notice of a memorandum of
October 17, 2005.
State program roles in ensuring If you need special accommodations understanding (MOU) between FDA and
appropriate use of radiation; facility due to a disability, please fax the Food and Drug Administration
quality assurance programs; and the information regarding those needs to Alumni Association, Inc. The purpose
establishment of a voluntary patient Kaye Chesemore at 301–594–3306, at of this MOU is to establish a greater
radiation dose reporting system for least 7 days in advance of the meeting. collaboration between FDA and the
diagnostic imaging procedures that use Food and Drug Administration Alumni
ionizing radiation. This system could be IV. Request for Suggestions, Association, Inc., regarding FDAs 2006
used to monitor national exposure Recommendations, and Materials Centennial Observance.
trends and provide a basis for FDA is particularly interested in DATES: The agreement became effective
establishing diagnostic reference levels receiving suggestions from stakeholders July 28, 2004.
of patient dose for use in facility quality related to the topics listed previously in
improvement programs. this document. Send suggestions or FOR FURTHER INFORMATION CONTACT:
• Monitoring the Industry— recommendations to the Division of Mary Hitch, Senior Advisor, Office of
Discussion will consider the following Dockets Management (see ADDRESSES). External Relations (HF–10), 5600
topics: The shift of FDA emphasis from FDA will place an additional copy of Fishers Lane, Rockville, MD 20857,
testing products, to inspecting any material it receives in the docket for 301–827–4406.
manufacturers to assure quality this document (2005N–0375). SUPPLEMENTARY INFORMATION: In
manufacturing and products; the Suggestions, recommendations, and accordance with 21 CFR 20.108(c),
reduction of reporting requirements; materials may be seen at the Division of which states that all written agreements
and the development of electronic Dockets Management between 9 a.m. and MOUs between FDA and others
reporting methods. and 4 p.m., Monday through Friday (see shall be published in the Federal
• Education—Discussion will ADDRESSES). Register, the agency is publishing notice
consider education and training for of this MOU.
manufacturers, regulators, and users. V. Transcripts
On November 1, 2005, FDA will hold Following the meeting, transcripts Dated: September 8, 2005.
concurrent discussion sessions will be available for review at the Jeffrey Shuren,
throughout the day on the Standards, Division of Dockets Management (see Assistant Commissioner for Policy.
Monitoring, and Education topics to ADDRESSES). BILLING CODE 4160–01–S
VerDate Aug<31>2005 15:21 Sep 22, 2005 Jkt 205001 PO 00000 Frm 00096 Fmt 4703 Sfmt 4703 E:\FR\FM\23SEN1.SGM 23SEN1
Federal Register / Vol. 70, No. 184 / Friday, September 23, 2005 / Notices 55911
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55912 Federal Register / Vol. 70, No. 184 / Friday, September 23, 2005 / Notices
EN23SE05.069</GPH>
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55914 Federal Register / Vol. 70, No. 184 / Friday, September 23, 2005 / Notices
[FR Doc. 05–19016 Filed 9–22–05; 8:45 am] SUMMARY: The Office of Rural Health activities under the second annual
BILLING CODE 4160–01–C Policy (ORHP), in cooperation with the Border Binational Health Week (October
Office of Global Health Affairs (OGHA), 10–16, 2005).
Office of Minority Health (OMH), Office FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND on Women’s Health (OWH), and Centers Elizabeth Rezai-zadeh, Office of Rural
HUMAN SERVICES for Disease Control and Prevention Health Policy, Room 9A–55, 5600
(CDC) will award a one year single Fishers Lane, Rockville, MD 20857.
Health Resources and Services
Administration source award to the U.S.-Mexico Border Telephone: 301–443–4107. E-mail:
Health Association (USMBHA) to erezai@hrsa.gov.
[CFDA 93.223] identify and promote best practices in SUPPLEMENTARY INFORMATION:
border communities. As defined in the
Cooperative Agreement for Border La Paz Agreement, the border region is Intended Recipient of the Award
Health Best Practices 100 km north and south of the U.S.-Mexico Border Health
AGENCY: Office of Rural Health Policy, international boundary line between the Association in El Paso, TX.
HRSA, DHHS. United States and Mexico. Funds will
be used on both sides of the U.S.- Amount of the Award
ACTION: Notice of Single Source Award.
Mexico border for the development of
EN23SE05.071</GPH>
$383,000.

Notice: Meetings: Food and Drug Administration and FDA Alumni Association

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Notice: Meetings: Food and Drug Administration and FDA Alumni Association

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55910 Federal Register / Vol. 70, No.

184 / Friday, September 23, 2005 / Notices

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