As a member of the 2D-BioPAD Consortium, Evnia hosts a webinar to discuss the basics of European Regulations for medical devices and in-vitro diagnostics.
🗓️10 February 2025
⏱️15:00-17:30 pm CET
Join us in an open discussion for
📌MD/IVD development roadmaps
📌the main challenges/bottlenecks associated with the current requirements
📌the current status of the regulations’ implementation and their impact on healthcare innovation
📌an exchange of views on strategies for the lifecycle management of medical products
