The European Commission’s In Vitro Diagnostic Regulation (IVDR) comes into full effect on the 26th of May, 2022. Genetic tests will now be classified as Class C, the second-highest class of devices, and health institution’s permissible use of laboratory developed tests (LDT) will change.

Speaker : Kim Rochat, Senior Partner at Medidee.

Join us for this webinar exploring how you need to adapt your wet lab and software to achieve compliance.

Register here