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SESSION 12: EU: PUBLIC DISCLOSURE IN UPCOMING NEW EU MEDICAL DEVICE REGULATION (MDR) AND IN-VITRO DIAGNOSTIC MEDICAL DEVICES REGULATION (IVDR)
Session Chair(s)
Matthias Zerm, PHD
Lead Expert, Clinical Trial Disclosure and R&D Processes
Germany
Speaker(s)
The Practical Side of Entering Data in the New MDR Eudamed
Ronald Boumans
EMERGO, Netherlands
Senior Global Regulatory Consultant
New Clinical Trial Disclosure Requirements for Medical Devices Trials
Erik Vollebregt, JD, LLM
AXON Lawyers, Netherlands
Partner