Medical Technology: Regulatory Affairs Workshop
How can start-ups in Medical Technology ensure future success?
The seminar will cover the following topics:
- Steps to CE Mark
- V&V and Technical Documentation
- Clinical Evidence
- US Market Access for Medical Devices
- Start-ups and Regulatory Affairs – Avoiding Pitfalls
This is your chance to acquire basic and some advanced regulatory know-how, that will help you to better understand the regulatory requirements of the health care market.
A joint event from Innovation in Health, Medidee Services, EIT Health RIH Germany-Switzerland and BadenCampus.