COCIR, together with MedTech Europe and five other associations, developed a joint position paper highlighting how the Medical Devices Regulation (MDR) and the In Vitro Diagnostics Regulation (IVDR) simplification proposal provide a more proportionate approach to life-cycle oversight.
Europe needs a regulatory system that protects patients while supporting innovation and competitiveness. The proposed simplification of the MDR and IVDR offers a more proportionate and efficient approach to life cycle oversight.