The
Division of Drug Information (DDI) is CDER's focal point for public
inquiries. We serve the public by providing information on human drug
products and drug product regulation by FDA.
On July 25, 2013, from 11:00AM-12:30PM (EDT), FDA will present a webinar on a new draft guidance entitled "Draft Guidance For Industry On Rheumatoid Arthritis - Developing Drug Products For Treatment; Availability."
The webinar will provide an
opportunity to learn about the guidance from individuals involved in
its preparation. It is also intended to encourage the submission of
questions or comments while the guidance is still in draft form.
Questions may be submitted online
during the webinar and will be addressed as time permits. All questions
should also be submitted to docket so that they can be formally
processed by FDA.
DRAFT GFI:
FR NOTICE
http://www.gpo.gov/fdsys/pkg/ FR-2013-05-31/pdf/2013-12922. pdf
For more information please visit: FDA Webinar
For more information please visit: FDA Webinar
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