Overview
This event will provide insight to the essential changes of the New Medical Device Regulation, such as the role of notified bodies and requirements in clinical and post-market requirements. Day One will be dedicated to key updates to MDR (Information Day), and Day Two will focus on developing skills to apply these regulation updates to attendees’ daily work (Interactive Hands-on Workshop).
Day One: MDR Information Day – Attendees will learn from key experts on the differences and new requirements within the new MDR.
Day Two: Hands-On Application Workshops – Attendees will work through practical application scenarios of the new updates with key subject matter experts.
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