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 is uniting medical device giants and innovative start-ups to share case studies and best practices in advancing and maintaining compliance of innovative software.

We will be shining 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, join 70+ CTOs, Heads of Software, Product, RA, and QA to harmonise cross-functional objectives, accelerate time to market, and optimise updates to legacy devices.

Event link here.