Tuesday 23.09.2025 | 09:00 - 17:00 | Microsoft Teams
AI offers huge opportunities for medical technology, but also lots of unanswered questions. How do I incorporate AI safely into my product? What do I have to consider with the AI Act, the MDR and data protection? And how does it all fit into my existing processes?
In our interactive seminar, hosted by Medical Mountains and together with seleon and our experts Rainer Duda and Jens Achenbach, you will get the answers. Concrete, understandable and practical.
- What does the AI Act require and how does it complement the MDR?
- How do you validate AI models in a comprehensible and secure way?
- What needs to be considered in data management, risk analysis and GDPR?
- How do you uncover and close gaps in your processes?
Who is it for?
For everyone who works in companies that develop medical devices with software and AI - e.g. in Regulatory & Quality Affairs, Risk Management, Requirements Engineering, Project or Product Management and Software Engineering.
Our goal:
You go out with a clear plan on how to get AI projects technically and regulatory on track in your company. Efficient, secure and future-proof.