The EU AI Act: What It Means for Medical Technology Suppliers and How to Get Ready

DATE: 19th November

Time: 2pm-3pm

Location: Teams

Host: Orcha

AXREM Members only

This webinar is a practical guide to the EU AI Act’s implications for technology manufacturers, covering risk classification under the Act, obligations for high-risk AI systems, transparency and documentation requirements, and a clear roadmap for achieving compliance. This webinar is particularly relevant for AXREM members with EU market presence or ambitions.