European Medical Device Regulation Workshop: Change Management 2016

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 split into small groups based upon key interest areas and work through practical application scenarios of the new updates with key subject matter experts. At the conclusion of each interactive workshop session, teams will reunite with the full conference to share out learnings and recommendations. Attendees can select a morning and an afternoon session from the specific topic areas highlighted below: - Clinical - Post-Marketing - Gap Assessment