IVDR state of play with a specific focus on companion diagnostics (CDx)

The In Vitro Diagnostics Medical Device Regulation 2017/746 (IVDR) updates the legal framework for all IVD medical devices intended to be placed on the European Single Market.

In this Deep Dive session, we will give you a general update on the state of play of the IVDR, specifically focusing on the experience with the EMA consultation procedure for CDx devices.

Date and time: Thursday, 27 October 2022, 4.00 pm (CEST) / 10.00 am (EDT)​​​​​​​

Your speakers: Marta Carnielli, IVD Technical Director

James Hewitt, Business Line Manager (IVD) & Senior Specialist (CDx)​​​​​​​

Register for free »