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Meeting Notice
Amended
Changes in the Agenda portion of the meeting.
| Center | Date | Time | Location |
|---|---|---|---|
| CDER | November 18, 2003 November 19, 2003 |
8 a.m. - 5 p.m. 8 a.m. - 12 noon |
Holiday Inn |
Agenda:
On November 18, 2003:
the committee will discuss the assessment and management of risk related to
QTc prolongation by Droperidol (Inapsine) Akorn, Inc., indicated for nausea
and vomiting in surgical and diagnostic procedures, premedication, and neuroleptanalgesia.
Background material and meeting information will become available no later than the day before the meeting (Simply select the appropriate committee link).
Closed Committee Deliberations:
On November 19, 2003, from 8 a.m. to 12 noon, the meeting will be closed to
permit discussion and review of trade secret and/or confidential information
(5 U.S.C. 552b(c)(4)).
Procedure:
On November 18, 2003, the meeting is open to the public. Interested persons
may present data, information, or views, orally or in writing, on issues pending
before the committee. Written submissions may be made to the contact person
by November 10, 2003. Oral presentations from the public will be scheduled between
approximately 1 p.m. and 2 p.m. Time allotted for each presentation may be limited.
Those desiring to make formal oral presentations should notify the contact person
before November 10, 2003, 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 requested to
make their presentation. Persons attending FDA's advisory committee meetings
are advised that the agency is not responsible for providing access to electrical
outlets.
FDA welcomes the attendance of the public at its advisory committee meetings
and will make every effort to accommodate persons with physical disabilities
or special needs. If you require special accommodations due to a disability,
please contact John Lauttman at 301-827-7001, at least 7 days in advance of
the meeting.
Contact Person:
Johanna M. Clifford, Center for Drug Evaluation and Research (HFD-21), Food
and Drug Administration, 5600 Fishers Lane, (for express delivery, 5630 Fishers
Lane, rm. 1093) Rockville, MD 20857, 301-827-7001, Fax: 301-827-6776 or email:
cliffordj@cder.fda.gov, or FDA Advisory
Committee Information Line, 1-800-741-8138 (301-443-0572 in the Washington,
DC area), code 12529. Please call the Information Line for up-to-date information
on this meeting.
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