The European market is capturing 30% of the global medical device field driven by rapid advances in innovative software, AI, and ML. But as medical device developers are met with tedious submission processes, ever-changing software patches, and red tape at every turn, it has never been more important to break out of cross-functional silos and stay two steps ahead of compliance guidelines.

Dedicated to unravelling a matrix of multi-layered European and global regulations, mitigating vulnerabilities in security, and managing updates to legacy devices, the 3rd Medical Device Software Development Summit Europe united medical device giants and innovative start-ups to share case studies and best practices in advancing and maintaining compliance of innovative software.

We shined the spotlight on:

• Working strategies shown through examples of documentation for AI enabled medical device software
• Implementing automation tools to establish feedback loops throughout the software development process
• Implementing rigorous data validation and cleansing processes to ensure reliability of training datasets for AI models
• Creating synergy between business and engineering through a unified data strategy

Uniquely positioned to share strategic guidance in optimising efficiency in regulatory submissions, streamlining development processes, and embedding compliant AI and ML in medical devices, 70+ CTOs, Heads of Software, Product, RA, and QA joined to harmonise cross-functional objectives, accelerate time to market, and optimise updates to legacy devices.