· 1 min read
Webinar: How to Deal with the New Post-Market Surveillance Requirements Under Regulation (EU) 2017/7
Industry expert Yue Li explains the new Medical Device Regulation 2017/745 that replaces the EU’s current Medical Device Directives (93/42/EEC and 90/385/EEC. She provides insights into how post-market surveillance is conducted, including an interface of PMS and technical documentation and a post-market clinical follow-up.
1 of 0