[Federal Register Volume 59, Number 18 (Thursday, January 27, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-1702]
[[Page Unknown]]
[Federal Register: January 27, 1994]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Advisory Committees; Notice of Meetings
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: This notice announces forthcoming meetings of public advisory
committees of the Food and Drug Administration (FDA). This notice also
summarizes the procedures for the meetings and methods by which
interested persons may participate in open public hearings before FDA's
advisory committees.
MEETINGS: The following advisory committee meetings are announced:
Dermatologic Drugs Advisory Committee
Date, time, and place. February 16, 1994, 8 a.m., conference rms. G
through J, Parklawn Bldg., 5600 Fishers Lane, Rockville, MD.
Type of meeting and contact person. Open public hearing, 8 a.m. to
9 a.m., unless public participation does not last that long; open
committee discussion, 9 a.m. to 12 m.; Ermona B. McGoodwin or Valerie
M. Mealy, Center for Drug Evaluation and Research (HFD-9), Food and
Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-443-
5455.
General function of the committee. The committee reviews and
evaluates data on the safety and effectiveness of marketed and
investigational human drugs for use in the treatment of dermatologic
diseases.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Those desiring to make formal presentations should
notify the contact person before February 11, 1994, and submit a brief
statement of the general nature of the evidence or arguments they wish
to present, the names and addresses of proposed participants, and an
indication of the approximate time required to make their comments.
Open committee discussion. The committee will discuss new drug
application NDA 19-821, Soriatane (acitretin), Roche
Dermatologics, for treatment of psoriasis.
Joint Meeting of the Dermatologic Drugs and Nonprescription Drugs
Advisory Committees
Date, time, and place. February 16, 1994, 1 p.m., conference rms. G
through J, Parklawn Bldg., 5600 Fishers Lane, Rockville, MD.
Type of meeting and contact person. Open public hearing, 1 p.m. to
2 p.m., unless public participation does not last that long; open
committee discussion, 2 p.m. to 5 p.m.; Ermona B. McGoodwin or Lee L.
Zwanziger, Center for Drug Evaluation and Research (HFD-9), Food and
Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-443-
5455.
General function of the committees. The Dermatologic Drugs Advisory
Committee reviews and evaluates data on the safety and effectiveness of
marketed and investigational human drugs for use in the treatment of
dermatologic diseases. The Nonprescription Drugs Advisory Committee
reviews and evaluates available data concerning the safety and
effectiveness of over-the-counter (nonprescription) human drug products
for use in the treatment of a broad spectrum of human symptoms and
diseases.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committees. Those desiring to make formal presentations should
notify the contact person before February 11, 1994, and submit a brief
statement of the general nature of the evidence or arguments they wish
to present, the names and addresses of proposed participants, and an
indication of the approximate time required to make their comments.
Open committee discussion. The committees will discuss new drug
application NDA 20-310, ketoconazole 1% shampoo, Johnson and Johnson
Consumer Products, for treatment of dandruff.
National Mammography Quality Assurance Advisory Committee
Date, time, and place. February 17 and 18, 1994, 8:30 a.m.,
Ballroom, Holiday Inn Metro Center, 775 12th St. NW., Washington, DC.
Type of meeting and contact person. Open public hearing, February
17, 1994, 8:30 a.m. to 9:30 a.m., unless public participation does not
last that long; open committee discussion, 9:30 a.m. to 5 p.m.; open
committee discussion, February 18, 1994, 8:30 a.m. to 5 p.m.; Charles
K. Showalter, Center for Devices and Radiological Health (HFZ-240),
Food and Drug Administration, 1901 Chapman Ave., Rockville, MD 20857,
301-594-3311.
General function of the committee. The committee advises on
developing appropriate quality standards and regulations for
mammography facilities.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Those desiring to make formal presentations should
notify the contact person before January 31, 1994, and submit a brief
statement of the general nature of the evidence or arguments they wish
to present, the names and addresses of proposed participants, and an
indication of the approximate time required to make their comments.
Open committee discussion. The committee will: (1) Discuss the
interim final standards for accreditation bodies and for facilities,
(2) receive status reports from FDA on activities related to
implementation of the Mammography Quality Standards Act of 1992 (Pub.
L. 102-539), and (3) discuss priorities for future standards.
Board of Tea Experts
Date, time, and place. February 24 and 25, 1994, 10 a.m., New York
Regional Laboratory, rm. 700, 850 Third Ave., Brooklyn, NY.
Type of meeting and contact person. Open public hearing, February
24, 1994, 10 a.m. to 11 a.m., unless public participation does not last
that long; open committee discussion, 11 a.m. to 4:30 p.m.; open
committee discussion, February 25, 1994, 10 a.m. to 4:30 p.m.; Robert
H. Dick, New York Regional Laboratory, Food and Drug Administration,
850 Third Ave., Brooklyn, NY 11232, 718-965-5730.
General function of the committee. The committee advises on
establishment of uniform standards of purity, quality, and fitness for
consumption of all tea imported into the United States under 21 U.S.C.
42.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee.
Open committee discussion. The committee will discuss and select
tea standards.
FDA public advisory committee meetings may have as many as four
separable portions: (1) An open public hearing, (2) an open committee
discussion, (3) a closed presentation of data, and (4) a closed
committee deliberation. Every advisory committee meeting shall have an
open public hearing portion. Whether or not it also includes any of the
other three portions will depend upon the specific meeting involved.
There are no closed portions for the meetings announced in this notice.
The dates and times reserved for the open portions of each committee
meeting are listed above.
The open public hearing portion of each meeting shall be at least 1
hour long unless public participation does not last that long. It is
emphasized, however, that the 1 hour time limit for an open public
hearing represents a minimum rather than a maximum time for public
participation, and an open public hearing may last for whatever longer
period the committee chairperson determines will facilitate the
committee's work.
Public hearings are subject to FDA's guideline (subpart C of 21 CFR
part 10) concerning the policy and procedures for electronic media
coverage of FDA's public administrative proceedings, including hearings
before public advisory committees under 21 CFR part 14. Under 21 CFR
10.205, representatives of the electronic media may be permitted,
subject to certain limitations, to videotape, film, or otherwise record
FDA's public administrative proceedings, including presentations by
participants.
Meetings of advisory committees shall be conducted, insofar as is
practical, in accordance with the agenda published in this Federal
Register notice. Changes in the agenda will be announced at the
beginning of the open portion of a meeting.
Any interested person who wishes to be assured of the right to make
an oral presentation at the open public hearing portion of a meeting
shall inform the contact person listed above, either orally or in
writing, prior to the meeting. Any person attending the hearing who
does not in advance of the meeting request an opportunity to speak will
be allowed to make an oral presentation at the hearing's conclusion, if
time permits, at the chairperson's discretion.
The agenda, the questions to be addressed by the committee, and a
current list of committee members will be available at the meeting
location on the day of the meeting.
Transcripts of the open portion of the meeting may be requested in
writing from the Freedom of Information Office (HFI-35), Food and Drug
Administration, rm. 12A-16, 5600 Fishers Lane, Rockville, MD 20857,
approximately 15 working days after the meeting, at a cost of 10 cents
per page. The transcript may be viewed at the Dockets Management Branch
(HFA-305), Food and Drug Administration, rm. 1-23, 12420 Parklawn Dr.,
Rockville, MD 20857, approximately 15 working days after the meeting,
between the hours of 9 a.m. and 4 p.m., Monday through Friday. Summary
minutes of the open portion of the meeting may be requested in writing
from the Freedom of Information Office (address above) beginning
approximately 90 days after the meeting.
This notice is issued under section 10(a)(1) and (2) of the Federal
Advisory Committee Act (5 U.S.C. app. 2), and FDA's regulations (21 CFR
part 14) on advisory committees.
Dated: January 21, 1994.
Jane E. Henney,
Deputy Commissioner for Operations.
[FR Doc. 94-1702 Filed 1-26-94; 8:45 am]
BILLING CODE 4160-01-F
