October 23, 2024 - October 24, 2024
/ Europe
Date: 23 and 24 October 2024
Location: Barcelona, Spain
Language: English
Introduction
The MDR and IVDR changes have added new requirements around clinical evaluation, risk management, and post-market surveillance, which continue to impact the regulatory affairs profession in Europe and elsewhere. Attending this conference will provide regulatory affairs professionals in medical devices with actionable solutions for these three pillars.
Keith Morel will host the 'Combined Postmarket Session' (11:45 AM – 12:45 PM CEST) on October 24th 2024.
For more information about the conference and to register, please visit the RAPS event website.
Qserve Attendee