How do you ensure innovation keeps pace with regulation? AI, software as a medical device, lifecycle management, post-market monitoring, clinical evidence, and real-world testing are no longer niche topics. They are central to the future of health technology.
The Developing Health Technology track at the Medtech Compliance Forum by Aurevia & RAPS brings together leading experts to discuss:
• MDR, IVDR and AI: navigating the regulatory landscape
• Governance and post-market monitoring of healthcare AI
• AI drift and lifecycle management
• Real-world testing and clinical evidence for AI devices
• MDSW Rule 11 and software compliance challenges
• EHDS requirements and software design implications
• Cybersecurity and SBOMs in medical device software
• AI in clinical practice: opportunities and lessons learned
Join experts from organisations including FIMEA, BioSciPons, SGS, Philips and Axon Lawyers as they share insights on how manufacturers can navigate a rapidly evolving regulatory landscape while continuing to innovate.
Explore the scientific programme
📍 Helsinki, Finland
📅 11-12 February 2027