TÜV SÜD Session – Ask us anything about Regulatory for Medical Device Software
TÜV SÜD - Ask us anything about Regulatory for Medical Device Software
December 10th, 2026
4:15 pm to 5:15 pm
CONFERENCE AREA 2
During this 1-hour session, you will be able to ask the speakers anything about your CE marking plans on your software. The 3 speakers will bring valuable insights from their own perspective and are:
- Marco Caproni, Global Director Software Products for TÜV SÜD
- Cyrille Michaud, Managing partner at MD101 Consulting
- A medical device software manufacturer
About TÜV SÜD
TÜV SÜD Medical Health Services provides testing, certification and regulatory expertise services to MedTech companies throughout the medical device lifecycle, with global laboratories and 30+ years of experience, we enable manufacturers to demonstrate compliance with applicable regulatory requirements and optimized access to global markets, TÜV SÜD’s testing and certification services are independent of each other and delivered by separate testing laboratories and certification bodies.
To access this session, you must be registered for MedFIT
To access this session, please register here
Sponsors
- 2026 Silver sponsor
