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
Introduction
Sponsorship & supporting organisations
ComplianceOnline
Venue
Online Event
Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
Contact information
Mr Referral
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email
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