Business Brunch – MDR: Focus on distributors and importers
Business Brunch with Miriam Schuh & Saskia Wittbrodt on 30 November 2018 in Düsseldorf
The much discussed European regulations for the medical devices industry have been in force now for over a year. As from May 2020 and 2022 respectively, the MDR and the IVDR will be applicable to the manufacture, placing on the market and monitoring of medical devices.
For importers and distributors in particular, the regulations bring new statutory obligations. At our business brunch we will be discussing the newly defined requirements and providing information about what it is that importers and distributors definitely need to pay heed to in view of the applicable regulations when designing their contracts with manufacturers.