NEU!! Entwickelt SxMDs mit einem strukturierten eQMS, einschließlich auditfähriger SxMD-Vorlagen, die an EU- und US-Standards angepasst sind. Mehr Erfahren!
High Risk AI under the European AI Act:
Must know strategies for Medical Device Companies to Achieve Regulatory Excellence.
In this on-demand webinar, you will learn:
What qualifies as high-risk AI under the AI Act.
The AI Act’s Regulatory Framework with insights into compliance requirements and reporting obligations.
Discover effective strategies for conducting risk assessments on AI technologies in medical devices.
How to future-proof your Regulatory Approach to stay ahead of the curve.
Who should attend:
Medical Device companies with AI
Head of RAQA
Head of R&D
Software as a Medical Device companies
C Suite & Cofounders