Supported by: Federal Ministry of Education and Research

Seminar series

What steps are required for an idea or invention from research to find its way into application? What framework conditions and regulatory requirements need to be considered and which partners may be needed to get closer to the goal of "application"? The seminar series will provide an overview of these questions and also address specific topics in the individual life science fields.

The event dates will be announced in time.

Between MDR and AI act: current EU regulations in medical device development

16.06.2025 13:00 Uhr -14:50 Uhr
Online
Free of charge

Vorträge:

MDR leicht gemacht – Ein praxisnaher Einstieg in die EU-Medizinproduktverordnung
Dr. Özlem Weiss, Expertants GmbH

EU AI Act: Knackpunkte zum rechtskonformen Einsatz von Künstlicher Intelligenz
Jonas Puchelt, FPS Law