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,” 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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