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On October 23rd, 2019 the MDR Support Panel will take place in the new sitem-insel building, Freiburgstrasse 3, 3010 Bern. The background to this event is the adoption of the new EU legislation in the field of medical devices (MDR), for which regulatory issues in particular have not yet been clarified.

The topic will be the regulation of third countries. As adoption of the framework agreement is not guaranteed, Swiss companies will have to develop a Plan B in order not to lose access to the EU internal market.

As a speaker, Hansjörg Riedwyl will present and discuss practical approaches to solutions with regard to possible coping strategies for Swiss industry. He will also take a stand on questions at the panel discussion.

Admission is free and registration is done with this form.

Further information can be found here.