Global Director Software Product Assessment
TÜV SÜD, Emilia-Romagna, Italy
Marco Caproni joined TÜV SÜD in 2018 as Product Specialist for active medical devices and he is the Senior Product Specialist for Software and AI. He is subject matter expert for all software-related products, including artificial intelligence technologies. He is also Global Director for Software Product Assessment team, leading the software, cybersecurity and AI experts in TÜV SÜD for medical devices and IVDs. In these roles, he leads comprehensive technical assessments, develops regulatory strategies, and authors guidance documents in alignment with the MDR/IVDR and relevant state-of-the-art standards. He has 15+ years of professional experience in the design and development of medical devices, in the area of software, extracorporeal circulation devices (such as dialysis) and has worked as software- and active medical devices-focused certification Lead Auditor and Technical Documentation Assessor.
Pre-Conference Workshop: Technical Documentation Assessment of MDSW-a Notified Body Perspective
Tuesday, May 5, 2026
08:30 - 16:00 WEST
Implementing the EU AI Act in Practice – A Catchbox Session
Wednesday, May 6, 2026
14:30 - 15:30 WEST