The new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you with this, in a two-part webinar series, starting on April 25.
Professor Herman Pieterse, Professor in Clinical Pharmacology at the University of Ghent and Iperion’s Managing Director, Frits Stulp, will explain on a high-level what the new regulations mean and provide you with insights on the business impact. The provided insights will allow you to understand the important changes and when it becomes effective, as well as the best ways to prepare for it.