Are you seeking a comprehensive guide for a smooth transition? The MDD to MDR gap analysis process helps identify differences between the requirements of MDD and the new Medical Devices Regulation (MDR) in the European Union. Our customizable template features three arrows, each representing a crucial topic in the transition process, making it a valuable asset to your toolkit. The MDD and MDR are regulatory frameworks governing the safety and efficacy of medical devices sold in the EU. Let our template help guide you through the transition and ensure compliance with MDR.
