Webinar: Navigating the EU AI Act – Key Impacts on MedTech

From August 2027, the EU AI Act will apply to devices undergoing conformity assessment
under MDR and IVDR.

Join us for an insightful webinar where we’ll discuss the EU Artificial Intelligence (AI) Act and its impact on medical device and IVD manufacturers, and don’t miss the chance to get ahead of the changes and prepare for the future of AI in medical technologies.

Webinar Details:
📅 Date: 2025-06-10
🕒 Time: 12:30 - 13:00 CET
📍 Location: Online (link provided upon registration)

Agenda:

✅Introduction to PharmaRelations and the Medical Device Team
✅ Understanding the EU AI Act – Overview of the Regulation and its Key Provisions
✅ Implications for Medical Device and IVD Manufacturers
✅ Compliance Strategies
✅ Q&A Session

This webinar is essential for anyone involved in regulatory affairs, quality, software engineering, or product leadership within the MedTech industry.

Register to the webinar

📩 Reserve your spot today! 
Let’s prepare for the future of AI in MedTech—see you there!