They will gain understanding:
- Recent developments around the AI Act
- Understand the applicable requirements
- Receive insight in the upgrade requirements for Technical Documentation and Quality Management Systems
Speaker
Leon Doorn has been working in the field of medical devices for over 15 years, focusing on quality and regulatory affairs. He holds a master’s degree in Life Sciences. For the last 10 years, he has been involved with Artificial Intelligence techniques implemented in medical devices. In 2024, he founded MedQAIR, a regulatory, quality, and information security consulting firm. Additionally, he serves as the chair of the Dutch working group on AI/ML-enabled medical devices, which is part of the Dutch JTC 21 & JTC1 SC standardisation committees.
EU AI Act: Current Status and Developments
- Recent developments around the AI Act
- Understand the applicable requirements
- Receive insight in the upgrade requirements for Technical Documentation and Quality Management Systems
Leon Doorn has been working in the field of medical devices for over 15 years, focusing on quality and regulatory affairs. He holds a master’s degree in Life Sciences. For the last 10 years, he has been involved with Artificial Intelligence techniques implemented in medical devices. In 2024, he founded MedQAIR, a regulatory, quality, and information security consulting firm. Additionally, he serves as the chair of the Dutch working group on AI/ML-enabled medical devices, which is part of the Dutch JTC 21 & JTC1 SC standardisation committees.