Median Technologies achieves ISO 13485:2016 certification for eyonis® Medical Device Quality Management System
• Certification of a robust and compliant Quality Management System for AI-based Software as Medical Devices, as per internationally recognized medical device regulatory standards
• Pledge of quality to support the industrialization, scaling, and deployment of Median’s eyonis® Software as a Medical Device portfolio
• Key milestone to pursue future regulatory approvals for the eyonis® portfolio and to deliver safe, reliable, and clinically meaningful oncology solutions
Sophia-Antipolis, France : Median Technologies (FR0011049824, ALMDT, “Median” or the “Company”), developer of eyonis®, a suite of artificial intelligence (AI)-powered Software as a Medical Device (SaMD) solutions for early cancer diagnosis, and a globally leading provider of AI-based image analyses and central imaging services for oncology drug developers, today announced it has achieved the globally recognized ISO 13485:2016 certification for its Quality Management System (QMS) applicable to AI-based Software as Medical Devices.