Webinar series - MDR made simple
A four-episode webinar series to help medical device manufacturers navigate MDR requirements with clarity and confidence.
The EU Medical Device Regulation (MDR) sets a high bar for demonstrating the safety, performance, and compliance of medical devices. For many manufacturers, the regulation’s scope and complexity can create uncertainty and leave critical compliance gaps unaddressed.
This MDR made simple webinar series is designed to bridge that gap. Across four focused sessions, our expert will guide you through the essential elements of MDR compliance, from classification and technical documentation to clinical evaluation and QMS alignment, providing practical steps you can apply immediately on your path to CE marking.
Watch the on-demand recording of four episodes to gain clear, actionable insights into classification, documentation, clinical evaluation, and QMS, the fundamental building blocks of MDR compliance.
