Getting a CE Mark for a traditional medical device is challenging enough, but the complexity multiplies when Artificial Intelligence is involved. This episode of MedTech Global Insights breaks down the intricate process of securing a CE Mark for AI-powered medical devices under the stringent EU Medical Device Regulation (MDR) and the new EU AI Act.

Imagine developing a groundbreaking AI algorithm that predicts patient outcomes with incredible accuracy, only to be stopped by a wall of regulations. Your training data is questioned for bias, the 'black box' nature of your AI concerns regulators, and the dual documentation requirements of the MDR and AI Act seem insurmountable. This is a common nightmare for MedTech pioneers, where brilliant innovation is at risk of being grounded by regulatory hurdles.

Key Takeaways:

* How is an AI-enabled medical device classified under the EU MDR, and why is this the most critical first step?

* What specific documentation is required for the algorithm's design, data validation, and risk management?

* How do you prove the safety and performance of a 'learning' algorithm that changes over time?

* What are a Notified Body's biggest concerns when assessing AI medical devices?

* How does the new EU AI Act intersect with the MDR, and what does it mean for your compliance strategy?

* What are the best practices for managing the clinical data used to train and test your AI?

* How can you build a robust Quality Management System that is fit for an AI-powered device?

For more information, contact us at [email protected] or visit https://pureglobal.com/.