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 pre- and post-market clinical requirements in the New Medical Device Regulation

Joris Bannenberg, MD, PhD

Factory - CRO for Medical Devices, Netherlands

Chief Medical Officer

注册方法

Registration fee includes refreshment break and delegate material.