This document is designed to help Swiss medical device manufacturers prepare for the regulatory scenarios they face with the renewal of the Mutual Recognition Agreement (MRA) uncertain before the new Medical Device Regulation (MDR) in the EU will apply from 26 May 2020. The solution finder will help you to identify the best solution for your business and the steps you should take now to ensure your product’s access to the EU market. This evaluation includes a 3-hour consultation with one of our specialists to answer your MRA/MDR questions and guide you through the evaluation process. The solution finder is ideal for manufacturers that are yet to prepare for the ‘third-country’ requirements.