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