Navigating AI in Medical Devices & Healthcare – From Hype to Harmonization!

Artificial Intelligence is rapidly transforming healthcare and medical technologies. While its potential is immense, the complexity it introduces poses real challenges for manufacturers and Notified Bodies alike. 

This 𝐃𝐐𝐒-𝐡𝐨𝐬𝐭𝐞𝐝 𝐰𝐞𝐛𝐢𝐧𝐚𝐫 offers a focused deep dive into the 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐃𝐞𝐯𝐢𝐜𝐞 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐢𝐨𝐧 (𝐌𝐃𝐑) 𝐚𝐧𝐝 𝐭𝐡𝐞 𝐧𝐞𝐰 𝐄𝐔 𝐀𝐫𝐭𝐢𝐟𝐢𝐜𝐢𝐚𝐥 𝐈𝐧𝐭𝐞𝐥𝐥𝐢𝐠𝐞𝐧𝐜𝐞 𝐀𝐜𝐭 — shedding light on their overlaps, critical gaps, and upcoming obligations. More than just an information session, it’s a dynamic exchange designed to align DQS with our customers and prospects, bringing clarity to the evolving regulatory landscape. Gain direct insights from industry experts, including Notified Body representatives, as we explore how AI impacts not only product design but also key supporting processes such as QMS, risk management, cybersecurity, and usability.