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 who 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?
We are happy to invite new and existing MVA members interested in joining us for our fourth network meeting where you will meet PCG Clinical Services, QAdvis, and SAXOCON, who will offer an overview of strategies to implement the new medtech regulations.
Joining the network is free of charge and is limited to Medicon Valley Alliance members. However, non-member organizations and companies are welcome to attend one network event to evaluate if being part of the network is relevant. If so, becoming a member of Medicon Valley Alliance will automatically able you to join the medtech network.