IVDR: Latest regulatory update - Part 1: General

The In-Vitro Diagnostics Medical Device Regulation 2017/746 updates the legal framework for all IVD medical devices intended to be placed on the European Single Market. This webinar will provide a general update on the status of implementation of the regulatory infrastructure required by the IVDR.  

Special focus will be placed on the recently published guidelines applicable to IVD manufacturers and on the implementation schedule up to the IVDR date of application. 


Date and time: Thursday, 11 November 2021, 9.30 am (CET)

Your speakers: Dr Andreas Stange | Vice-President
                              Marta Carnielli | IVD Technical Officer

Registration »