Do you want to know what the rules and regulations entail when introducing a medical device into the market? Apply for this hybrid seminar course held by specialists from academia and industry with 10 different seminar topics:
- Introduction to the Medical Device Regulation
- Risk Management
- Clinical Evaluation
- Software for medical devices
- Medical devices in the field
- Quality Management
- 3D-Printing in Medical Engineering & Artificial Intelligence
- Other Countries, Other Customs
- Usability Engineering
- Systematic MDR-Compliant Medical Product Development
Registration open until 25.09.2025