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Q&A | Impact of the EU AI Act on Medical Device and IVD Manufacturers

The EU AI Act is a proposed regulation by the European Commission aimed at ensuring that AI systems used within the European Union are safe, transparent, and uphold fundamental rights. It classifies AI systems into different risk categories and imposes varying levels of regulatory requirements based on the potential impact of these systems.

AI is becoming an integral part of our daily lives, and its governance affects everyone from tech giants to individual users. The EU AI Act is set to become a benchmark for AI regulation globally, influencing policies in other regions as well. Staying informed about these regulations can help you navigate the changing landscape of AI technology responsibly and effectively.

Watch the Q&A with Software and AI Expert Coenraad Davidsdochter, diving into several top-asked questions about the EU AI Act.


Coenraad Davidsdochter, MSc
Date d'envoi: juillet 30, 2024
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