23rd-24th October 2024 | Barcelona, Spain
The two-day conference curated by RAPS European Council (REC) is targeted at providing the attendees actionable insights in respect to the MDR and IVDR changes. The new requirements around clinical evaluation, post market surveillance and risk management continue to impact regulatory affairs domain in Europe and elsewhere.
By attending the conference, you will also get the opportunity to engage with partners, connect with decision makes as well demonstrate your expertise.
Speaker session
Topic: How to Conduct CDx Clinical Performance Studies in Compliance with IVDR 2017/746?
Wednesday, 23 October 2024 | 1:45 PM – 2:45 PM CEST
Piritta Maunu
Senior Manager, Regulatory Affairs, Medical Devices, Team Lead UK & Nordics
Register here: https://www.raps.org/eucrps/home
