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| Center | Date | Time | Location |
|---|---|---|---|
| CDER | March 4, 2003 | 8:30 a.m. - 3:30 p.m. | Center for Drug
Evaluation and Research |
Agenda:
The subcommittee will discuss pediatric labeling for oncology products.
Procedure:
Interested persons may present data, information, or views, orally or in writing,
on issues pending before the subcommittee. Written submissions may be made to
the contact person by February 24, 2003. Oral presentations from the public
will be scheduled between approximately 10 a.m. and 11 a.m. Time allotted for
each presentation may be limited. Those desiring to make formal oral presentations
should notify the contact person before February 24, 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 Thomas Perez at least 7 days in advance of the meeting.
Contact Person:
Thomas H. Perez, 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, 301-827-6758, or e-mail: PerezT@cder.fda.gov,
or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in
the Washington, DC area), code 12542. Please call the Information Line for up-to-date
information on this meeting.
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