The New Medical Device Regulation Information Day

This Information Day is designed for regulatory professionals (e.g. medical device industry, pharma industry, trade associations, notified bodies, authorities etc.), who would like to be updated on the changes and implications of the new EU Medical Device Regulation.

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Speaker(s)

Changes in vigilance and post-market requirements in the New Medical Device Regulation

Reinhard Berger, DrSc, MSc

Consulting-Advising, Austria

Regulatory Affairs Medical Devices

注册方法

Registration fee includes refreshment break and delegate material.