With the new version 10.4, the established medical device classifier is now also available for in vitro diagnostics and thus for the determination of risk classes A to D based on EU Regulation 2017/746 (IVDR). The new classifier can be found in the risk management plan under the additional menu item “Classification IVD”.

Our Expert:inn for the convenient generation of technical documentation for medical devices will show you the most important innovations in version 10.4 live on the system on January 26, 2022 from 11:00 to 12:00 and will be available to answer your individual questions.

Register now free of charge: