sitem-insel AG

3/19 MDR Support Panel: Third Countries Regulation


October 23, 2019


sitem-insel AG
Auditorium Ground Floor
Freiburgstrasse 3
3010 Bern


Free admission

The MDR Support Panel presents and discusses various solutions for the implementation of the MDR concerning Third Countries Regulation.


By e-mail to until October 18, 2019



The adoption of the new EU legislation on medical devices (MDR) and in-vitro diagnostics (IVDR) has a direct impact on Swiss manufacturers, suppliers, importers, authorities, hospitals and patients. In particular, regulatory issues are unresolved or unknown for many market participants. To achieve pragmatic solutions, sitem-insel and Swiss Medtech host the MDR Readiness Day and the MDR Support Panel.



During the MDR Readiness Day, topic-specific questions from representatives of SMEs will be dealt with, while consultants and Notified Bodies will take a stand on the questions in the MDR Support Panel and point out possible solutions.