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April 30, 2019 - May 3, 2019
Actionable insights on these topics and more:
FDA Mock Inspection: Knock Knock! Guess Who’s at Your Door
Center Director Corner: Strategic Priorities for 2019 and Beyond
EU MDR: Successful Practices for Procedural Hurdles
The Business and Innovation of Digital Health
FDA Office of Medical Device and Radiological Health Operations Update and Strategic Priorities
Beyond MDSAP and ISO 13485 and the Impact of the New EU Regulations
Follow the Defect: Case of the Missing Cavity
Getting Your Product on the Market: Premarket Approval is Only the Beginning
Successfully Navigate the Medical Device Recalls Process: An Interactive Case Study