During the Barcelona Health Innovation Week, Asphalion hosted an insightful workshop on “Regulatory Tips for AI & Software-Based Medical Technologies.” Experts from diverse backgrounds came together to delve into the regulatory landscape of AI in medical devices.
Among the speakers was Asphalion’s own Medical Device Associate Director, Josefa Güiles Muñoz. She shared her extensive knowledge on the regulatory processes and roadmaps essential for AI-based medical devices.
In this video, she goes through the regulatory pathway of Medical Devices, specially now that these are evolving at a high speed due to materials, incorporation of new technologies, algorithms, etc.
Furthermore, the EU new regulation have brought many changes and it is essential to adopt them asap.
Watch this short clip of her detailed insights on regulatory compliance in AI-based medical technology and key learnings from the workshop here: AI WORKSHOP
If you need any assistance with your medical devices, please contact us at: [email protected]
