6^th Annual European Medical Device and Diagnostic Clinical Evidence Strategy Conference

"Well-organised, interesting and well-balanced agenda."

"Valuable insights were offered on the most critical changes in MDR, and it was useful to learn how IIS can be used for regulatory purposes. It was a great opportunity to interact with fellow industry members."

“Very well organised. Great variety of related topics and good interaction opportunities.”

"Networking is a good way to get another external opinion."

"A small group, but very consistent in profile - medical devices & clinical studies. Exchange was promoted, there were good speakers, and the presence of NB representatives in active discussions was a very good addition."

"Having experts from the industry, Notified Bodies, and Authorities is of great value because it provides a forum for an open discussion on requirements, interpretations & implementation."