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Required steps to get your medical device on the market
We are so honored to be invited to collaborate with MVA, Medicon Village Alliance to participate in their next event in Denmark on June 11th.
Over the coming years new medtech regulations – Medical Device Regulations (MDR 2017/745) and in-vitro Diagnostic Regulations (IVDR 2017/746) – come into effect and everyone that wish to have a medical device or an in-vitro diagnostic device on the market needs to relate to these requirements. Do you have a strategy for your MDR- and IVDR-transformation?
Date: 11th of June, 2018
Time: 17.00- 20.00
Hosts: Medtech Innovation and SAXOCON
Venue: Meeting room 1, 2nd floor, Meeting Center, Building 101 (Entrance A), Technical University of Denmark, Anker Engelunds Vej 1, Kgs. Lyngby – Map