This training provides you with the basics of regulatory affairs in MedTech with the focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation). Get an overview of the regulatory landscape, hear about the basic concepts and principles and get insights into the necessary steps but also pitfalls when bringing a MedTech product to the market. Discuss with the experts.
- Researchers in the field of translational medicine
- Employees from spin-offs, start-ups and SMEs, who intend to bring a product to the market
- Employees from companies interested in getting an overview on regulatory affairs
- Investors in medical devices who would like to understand risks and opportunities regarding the evolving regulatory framework in EU
This workshop is free of charge.
Organizers & Partner