The MDR Support Panel presents and discusses first experience with the impelmentation of MDR.
To register please fill out this Form until January 9, 2020
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.