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.
๐๏ธ10 February 2025
โฑ๏ธ15:00-17:30 pm CET
Join us in an open discussion for
๐MD/IVD development roadmaps
๐the main challenges/bottlenecks associated with the current requirements
๐the current status of the regulations’ implementation and their impact on healthcare innovation
๐an exchange of views on strategies for the lifecycle management of medical products
