MDR

Last changed on 20 September 2023 - 14:57

The European Union Medical Device Regulation (EU MDR) is a comprehensive regulatory framework that aims to strengthen patient safety and ensure the effectiveness of Medical Devices marketed in the EU.
In force since May 2021, the EU MDR replaces the Medical Devices Directive (MDD) and the In-Vitro Diagnostic Medical Devices Directive (IVDD), bringing significant changes and implications for various stakeholders, including distributors.