This Information Day will give clear and practical updates on how to develop a medical device and how to identify the correct development path under the new Medical Device Regulation.

You will get an overview of the EU device legislative changes. This Information Day will provide an insight of the essential changes in various fields, such as the role of notified bodies and requirements in clinical or post-market requirements.

Who Should Attend

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.