Navigating the regulatory jungle: AI in MedTech between the AI Act and MDR

The complexity of the regulatory landscape is increasing and the need to navigate between the AI Act and the Medical Device Regulation (MDR) is becoming more complex. We want to shed light on specific requirements as well as solutions for the regulation of AI in different contexts.

13:45-14:00 Immersive AI in medical technology - practical example: How MedTech organisations and device manufacturers benefit from training with generative AI
Andreas Mose (Medverse)

14:00-14:15 More than just Precision, Recall & F1-Score: Governance & Responsible AI as important building blocks for safe and compliant AI systems in medical technology
David Mack (Philips) Veit Mengling (d-fine)

14:15-14:30 Intelligence meets (medical) technology: Use cases and safety aspects for the use of AI in medical technology
Radi Achkik (Xitaso)

 14:30-14:45 AI validation and quality assurance: Do you know what your AI is doing?
Konstanze Olschewski (Phnx Alpha GmbH) 

Please note: the lecutres will be held in German. The lectures will be translated into English via voice-to-text so that you can follow the lecture live in written form via a monitor.

Supported by: bitkom e.V.