Venue: Meeting room 1, 2nd floor, Meeting Center, Building 101 (Entrance A), Technical University of Denmark, Anker Engelunds Vej 1, Kgs. Lyngby
Time: 17:00 - 20:00
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?
MVA is happy to invite new and existing MVA and DANSK BIOTEK members interested in joining for the fourth network meeting where you will meet PCG Clinical Services, QAdvis, and SAXOCON, that will offer an overview of strategies to implement the new medtech regulations.