On 21 May 2024, the EU Council approved the AI Act — a major of regulatory law that defines comprehensive rules on artificial intelligence and relevant technologies. The AI Act has a risk-based approach, ensuring the transparency, reliability and accountability of the technology, bringing the sector-specific requirements. Considering that the softwares as medical devices are becoming one of the brightest stars in medical device area, the new AI Act is clearly a new era and shall be evaluated to ensure the compliance with the regulations.


We look forward to seeing you in our free webinar on June 19, 2024 at 16.00 CET, to discuss what the new AI Act brings and effects on softwares as medical devices… The webinar will be held in English and delivered by Ozer Kircak. 

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