Fusing Knowledge from Software, QA, RA & Product Teams to Align Innovation in Software with Evolving Process, Cybersecurity & Global Regulatory Frameworks

27th-29th January, 2025 | Munich, Germany

Welcome to the 3rd Medical Device Software Development Summit Europe

Integrating Expertise from Software Development, Quality Assurance, Regulatory Affairs, & Product Teams to Drive Innovation in Alignment with Global Regulatory Guidelines, AI & ML Enabled Software, Cybersecurity, & Agile Methodologies

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.

Snapshot of the Expert Speaker Faculty:

Testimonials From Past Participants Across our Medical Device Series:

"Overall knowledge/quality of the presenters and the presentation topics were current and super relevant. Interactive Q&A at end of each presentation, and opportunity to network with presenters during breaks."

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Baxter

"Really high quality of speakers and talks were exceptional."

"Three extraordinary days of fantastic expert discussions created an exceptional, software-focused conference."

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