Medical Technology: Regulatory Affairs 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.

Agenda & Registration: https://www.eventbrite.com/e/medical-technology-regulatory-affairs-workshop-tickets-302574597767

Login-Details will be sent to the registered attendees.

Presentation: Medidee Services

Moderation: Ida Scholz & Sebastian Meuer

Language: English

Supported by the Ministry of Science, Research and the Arts Baden-Württemberg

The Go-To-Market Academy is an online seminar series from Innovation In Health. All seminars are held by experts in their field and are free of charge!