Regulatory Affairs Info Session
Lead regulatory strategy in the evolving medical device industry.
As global regulations become increasingly complex, professionals who can navigate FDA, EU, and international requirements are in high demand. Learn how to design and execute regulatory strategies, manage premarket submissions using tools like the FDA’s eSTAR, leverage AI-driven platforms for regulatory intelligence, and ensure compliance across device lifecycles.
Speaker
Join Kiran Gulati, chair of the UCSC Silicon Valley Extension Regulatory Affairs program, for a detailed overview of how our courses provide practical, hands-on training and industry-aligned skills to advance your career in regulatory affairs, quality assurance, and medical device compliance.
Start exploring
Check out our Regulatory Affairs certificate program page for a closer look at upcoming courses and offerings.
