High Risk AI under European AI Act: Must know strategies for Medical Device Companies

Описание к видео High Risk AI under European AI Act: Must know strategies for Medical Device Companies

In this 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

https://matrixreq.com/blog/ai-act-med...

Комментарии

Информация по комментариям в разработке

Похожие видео