This webinar will review the similarities and differences in the regulatory paths and requirements for drugs, biologics and medical devices. It will discuss the applicable FDA "Centers,鈥� the IDE and IND process, as well as 510k, PMA, NDA and BLA submission processes.
Regulatory Differences Between Biopharmaceutics and Medical Devices
8 August 2013, Palo Alto, United States
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ComplianceOnline
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Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
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