

MedEnvoy
Events & Updates
- Full length webinar - watch on YouTubeWATCH NOWWhen 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
- 7 MinutesWATCH NOWBrief overview of Swiss importer and CH-REP requirements for medical device and IVD manufacturers by Edgar Kasteel, Co-Founder of MedEnvoy
- 30 minutesWATCH NOWEdgar 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.
- 20 MinutesON YOUTUBEEdgar Kasteel, Managing Director of MedEnvoy, goes over the details of how to ensure you are meeting the importer requirements of the EU MDR.
- 35 MinutesLISTEN NOWRene van de Zande, a Partner with MedEnvoy, talks to Jon Speer from Greenlight Guru about the role of the EU importer.
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