Medical Technology: Regulatory Affairs Workshop
Basics of Regulatory Affairs for Start-ups in Medical Technology – a two days workshop
How can start-ups in Medical Technology ensure future success? By acquiring regulatory know-how as early as possible! Why is regulation so important for medical technology products? Why should regulatory requirements be addressed as early as possible? What is important?
Among others, 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.
Register now for free!
Presentation: Peter Hartung, Leiter der Business Unit Consulting Seleon GmbH
Moderation: Ida Scholz & Sebastian Meuer
Language: English
Supported by the Ministry of Science, Research and the Arts Baden-Württemberg
