FDA discusses pharmaceutical quality and new innovations in regulatory science. Includes responses to audience in a question-and-answer panel.
Presenters, from OPQ, and presentations include:
Emerging Technology Program 2.0
Sau “Larry” Lee
Addressing the Advanced Manufacturing Regulatory Framework
Adam Fisher, PhD
Q&A Panel (Includes all above presenters)
For slides and additional information: [ Ссылка ]
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FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.
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Email - CDERSBIA@fda.hhs.gov
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