IVDR: Latest regulatory update - Part 1: Class D, novel Class C

Class D, CDx and novel Class C devices represent high-risk IVDs with additional requirements under the IVDR. This webinar will discuss the latest information regarding these additional requirements to enable manufacturers to prepare for their conformity assessment projects more effectively. As part of this webinar, we will cover the current information on the EMA consultation procedure for CDx devices, the transitional provisions for Class D devices and considerations for novel Class C devices. 


Date and time: Thursday, 11 November 2021, 10.30 am (CET)

Your speakers: James Hewitt | IVD Product Expert
                             Dr Eric Heilmann | IVD Clinical Reviewer

​​​​​​​Registration »