Our Publications
The EU AI Act
In-depth overview of the EU AI Act, focusing on its implications for medical device manufacturers. It details the Act’s risk-based classification of AI systems, key obligations for high-risk AI systems, and compliance strategies for manufacturers, including data governance and risk management. This essential guide helps manufacturers navigate the new regulatory landscape, ensuring their AI technologies are safe, effective, and compliant.
This guide partners well with our webinar: “Navigating the AI Regulatory Landscape” focused on the EU AI Act.
