
As healthcare technology evolves, professionals who understand global regulatory standards, risk management, and quality systems are in high demand. Learn how to design, document, and validate medical devices, digital health solutions, and AI/ML-based devices while ensuring compliance with FDA, ISO, and EU MDR requirements.
Join Kiran Gulati, chair of the UCSC Silicon Valley Extension Medical Device Quality and Design program, for an inside look at how our courses provide hands-on training, practical case studies, and industry-relevant skills that prepare you for roles in quality engineering, regulatory compliance, and design assurance.
This winter info session is sponsored by the Medical Device Quality and Design certificate program.