Are you prepared for the new EU medical device regulation? Niels van Tienen, Factory Project Manager, will be presenting at the DIA Interactive Hands-on Workshop on European Medical Device Regulation - Change Management (29-30 November 2016, Vienna, Austria).
This workshop 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, and will learn you how to correctly apply the updates to your daily work. The course is designed for professionals heavily involved in the development and bringing to market of medical devices and combination products. Day 1 of the workshop will be dedicated to key updates to MDR. Day 2 will focus on developing skills to apply these regulation updates to attendees’ daily work by ways of hands-on application workshops.
Do you want to meet Niels at the congress? Contact him in advance.Visit event page