FDA Small Business Regulatory Education for Industry (REdI): Generic Drugs Forum 2016
For slides from this event, click here
This two-day FDA-led forum offered you the opportunity to interact with FDA subject matter experts as we discussed various topics along the dynamic continuum of the generic drug approval process.
Keynote Speaker: Kathleen Uhl, M.D. Director, Office of Generic Drugs, CDER, FDA
Topics include:
- Communication with Industry
- Current Trends in Labeling and Best Practices
- GDUFA Regulatory Science
For more information on
(866)-405-5367 | (301)-796-6707 | CDER Small Business and Industry Assistance CDERSBIA@fda.hhs.gov