The MDR Support Panel presents and discusses various solutions for the implementation of the MDR concerning third party country requirements.
To register please fill out this Form 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.