sitem-insel AG

3/19 MDR Support Panel: Third Party Country Requirements

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DATE

October 23, 2019

PLACE

sitem-insel AG
Auditorium Ground Floor
Freiburgstrasse 3
3010 Bern

The MDR Support Panel presents and discusses various solutions for the implementation of the MDR concerning third party country requirements.


REGISTRATION

To register please fill out this Form until October 18, 2019

 

BACKGROUND

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.

 

CONCEPT

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.