Ms. Ajda Mihelčič

Deputy Manager

Publishing Department

SPEAKERS

Mr. Eric A. Klasen 

Obelis Chief Executive Officer CH 

Obelis GmbH

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Complying with the EU Market Regulations can be a daunting task to undertake on your own. Make sure you get all the information you need. 

We bring our experience and knowledge in the medical devices and in-vitro diagnostics industries, so don't miss the webinar!

33 YEARS OF QUALITY

SERVICE IN REGULATORY AFFAIRS

In this webinar, we will provide an overview of:​

• What EU/ Non-EU (non-Swiss based) companies need to do to enter the Swiss market with their medical devices? Timeline with no MRA in place & how Obelis Swiss as CH-REP can help you
• What Swiss companies need to do to enter the EU market? Timeline & how can Obelis help as EU AR  
• FAQ on the most important aspects of the new regulatory framework in Switzerland: Feedback from the Swiss Competent Authority to help manufacturers better understand how to comply

How MDR & lack of MRA update affect medical device trade? 

Webinar: EU- Swiss MRA Latest 

EU- SWISS MRA LATEST

FREE!