Nouveauté ! Développez votre produit SxMD avec un eQMS structuré comprenant des modèles SxMD prêts à être audités et conformes aux normes EU et US. En savoir plus !
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
United States
United Kingdom
France
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Spain
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United Arab Emirates
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Uzbekistan
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Holy See (Vatican City State)
Venezuela
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Wallis and Futuna
Yemen
Zambia
ZimbabweClick this link to watch the webinar on demand.
