The MDR Support Panel presents and discusses various solutions for the implementation of the MDR concerning Combination Products.
Manufacturers of combination products will face many new challenges with the new MDR. Find out what you need to pay attention to in your products.
16:30 – Admission
17:00 – Presentations and panel discussion
18:30 – Reception
By e-mail to MDR@sitem-insel.ch until June 21, 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.
Please find further information here.
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.