A forum for expert exchange in medical device regulation
In a regulatory environment that continues to evolve, the exchange of information and experience remains an important basis for informed decision-making. Professionals working in medical device sector are required to stay up to date with regulatory developments while maintaining a structured approach to compliance and quality.
We think that direct dialogue is an essential element of effective knowledge sharing. For this reason, we would like to invite you to the Consultation Day Medical Devices 2026 at the TÜV NORD site in Essen.
The event offers consultants and regulatory affairs specialists involved in medical device technology, regulatory affairs, quality management, and topics such as MDR and IVDR the possibility to connect and discuss all the relevant topics. Participants will also receive insights into medical device certification and conformity assessment from the perspective of TÜV NORD as a Notified Body.
Participation is free of charge, but places are limited. Therefore, we recommend registering early if you would like to join the event and exchange with other professionals.
