Invitation｜Strategies for MDR/IVDR Success

In recent years, the European Union has upgraded comprehensively regulations in the fields of medical devices and in vitro diagnostic devices. And how to meet the requirements of the new regulations has become a great challenge for Chinese medical device manufacturers. We sincerely invite you to attend the seminar “Strategies for MDR/IVDR Success” hosted by PYQ Lab and IMQ (Italian Notified Body CE-MDR NB0051), as well as co-sponsored by Suzhou Industrial Park Enterprise Joint Open Innovation (SIP ENJOI) in the afternoon of July 26th, 2024. It is aimed at navigating the new regulatory challenges for Chinese MedTech companies and speeding up the compliance process for successful CE marking.

The seminar is free of charge both online and offline, and we are looking forward to your active participation.