As artificial intelligence (AI) continues to play an increasingly vital role in society, ensuring its reliability, safety, and ethical use has become paramount. This talk provides an overview of the standardized frameworks and methodologies used to evaluate and validate AI yechnology in medical devices. Attendees will gain a deeper understanding of the evolving landscape of AI certification and its implications for shaping the future of AI technology.
Modern in-vitro diagnostic processes rely heavily on features implemented in software. Improving the software quality is the way to improve the diagnostics results and also stay compliant with the upcoming IVDR regulations.