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