When the EU MDR and IVDR were published in 2017 these regulations elevated the role of two critical economic operators; distributor and importer. Subsequent to the release of the EU regulations Brexit (UK) and Swixit (Switzerland) happened, introducing new, country-specific requirements for medical

Brief overview of Swiss importer and CH-REP requirements for medical device and IVD manufacturers by Edgar Kasteel, Co-Founder of MedEnvoy

Edgar Kasteel, Managing Director of MedEnvoy Global, sits down (virtually) with Monir El Azzouzi from Easy Medical Device to talk about the EU Importer role under the MDR.

Edgar Kasteel, Managing Director of MedEnvoy, goes over the details of how to ensure you are meeting the importer requirements of the EU MDR.

Rene van de Zande, a Partner with MedEnvoy, talks to Jon Speer from Greenlight Guru about the role of the EU importer.