Group IVDR Manager
Unilabs
Marta specialises in EU regulatory field under Regulation (EU) 2017/746 (IVDR). Background in In-Vitro Medical Device industry from the manufacturers side from more than 10 years and currently working for a private leading international provider of laboratory diagnostic services. Marta is leading all the work of compliance of in-house tests and software developed across all laboratories in Europe in compliance with Article 5(5) of the IVDR.
Disclosure information not submitted.
Experience Gain From Implementing Article 5(5) of the IVDR in a Network of European Laboratories
Wednesday, May 8, 2024
14:00 – 15:00 CEST