Go-To-Market Academy

Generating and using evidence is one of the most important steps for medtech companies on their way to the market. And even when on the market, evidence remains an issue in terms of post market surveillance. This seminar provides you with an overview of the necessities of clinical studies. Our partners from Profil GmbH will cover regulatory and ethical requirements, share theoretical knowledge and their experience from the development phase of a medical device. Profil GmbH has been involved in several innovation processes and combines long-term clinical experience with the needs of innovation project consortia.

A joint event from Innovation in Health, Profil GmbH and EIT Health RIH Germany-Switzerland.