Guy leads AIQ’s software development and technical strategy, overseeing the design and delivery of clinical-grade software for regulated healthcare environments.

With extensive experience in full lifecycle development of FDA-regulated medical device software, Guy has led the architecture, development, and validation of complex systems across both industry and academic settings. He played a central role in AIQ’s FDA 510(k) clearance, including the development of the company’s software quality systems, clinical-grade technology and cybersecurity.

His background includes leadership roles in software architecture, product development, and process design, with experience spanning medical devices and other highly regulated industries.