As part of EU reforms in recent years, the Medical Device Directive (MDD) has been upgraded to the Medical Device Regulation (MDR), which significantly increases the requirements for safety, performance, clinical evaluation and life cycle of medical devices. TÜV Rheinland, one of the world’s leading providers of testing and certification services, offers manufacturers and distributors of medical devices to check their products for MDR conformity.
MEdizinprofukt