IVDR & Immunoassays Mini-Symposium
Surely you have heard about it: the IVD, the new In Vitro Diagnostic Medical Devices Regulation. Published in May 2017, it replaces the In Vitro Diagnostic Medical Devices Directive (IVDD) and brings new requirements for manufacturers. The good news is: there is a five-year transition period. But do you know how this affects you, and how you will make sure you are fully compliant by 2022?
At MEDICA we organized the first IVDR & Immunoassays Mini-Symposium together with Qarad and Tüv Süd.