16 October 2025 | Blog postMDR made simple: Why device classification shapes everything that follows
The EU Medical Device Regulation (MDR) sets a high standard for demonstrating the safety, performance, and compliance of medical devices. To support manufacturers in meeting these requirements, DNV launched the MDR Made Simple webinar series, a four-episode programme offering practical insights into classification, documentation, clinical evaluation, and quality management systems, the essential foundations of MDR compliance.