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.

Day 1 (Thuesday 14.06.2022)

9:30 Opening & Welcome

9:45 - 12:00 Workshop Part 1

12:00 Q&A

Day 2 (Wednesday 15.06.2022)

9:30 Opening & Welcome

9:45 - 12:00 Workshop Part 2

12:00 Q&A

Register now for free!

Login-Details will be sent to the registered attendees.

Presentation: Medidee Services

Moderation: Ida Scholz & Sebastian Meuer

Language: English

To register click here

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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!

Next seminar: "From the idea to the successful medical device - learning from the mistakes of others" will take place on 20.06.2022.