Clinical and Regulatory Affairs

The Clinical and Regulatory Affairs team at Medo.ai ensures that the company's innovative ultrasound technologies meet stringent regulatory standards while providing exceptional clinical support. This team focuses on developing and implementing quality management systems, overseeing clinical education initiatives, and facilitating the necessary regulatory submissions. They also engage in the analysis and annotation of medical images to enhance product accuracy and compliance, ultimately aiming to optimize patient care and ensure the safe use of Medo's AI-driven diagnostic solutions.