Skip to main content

Morning Coffee Seminar – EU AI Act: Current Status and Developments

Join us for an informative and practical discussion aimed at helping you better understand the impact of the AI Act on the health technology sector. The session will be led by Leon Doorn, CEO and Co-Founder of MedQAIR, who will share his expertise and insights on navigating this evolving regulatory landscape. The seminar will be 1.5 h long. This time all the spots are taken. We will record the seminar and add it to this page.

Date
29. August 2025, 09:00
Language
English
Location
Öpik Conference Center / Valukoja 8, Ülemiste City, Tallinn (Room: Universum)
Cost
Free
Status
Registration closed
Fully booked

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, CEO and Co-Founder of MedQAIR

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, CEO and Co-Founder of MedQAIR

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.

Contact

Contact

Sandra Ruul
Digitalisation Project Manager