How to Read the MDR

Understanding the EU MDR can feel overwhelming, especially when navigating the different Articles and Annexes. In this video, we break down how to read and interpret the Medical Device Regulation (MDR), including the structure of the regulation and where to find key requirements related to compliance, technical documentation, clinical evaluation, post-market surveillance and more. Whether you’re new to MDR or looking for a clearer way to navigate the regulation, this overview will help simplify the process.