Regulatory Affairs and Medical Devices Info Session

Interested in a career that combines biology, new technology, project management and discovery?

Join us for a brief overview of two high-demand industries—Regulatory Affairs and Medical Device Quality and Design.

You’ll meet Kiran Gulati, a medical device consultant with 30 years of experience who is also the chair of two exciting professional certificate programs: Regulatory Affairs and Medical Device Quality and Design. She’ll cover the skills and courses you can take to get going in these careers or what you need to know to pick up again after a pause in your career.

Learn the knowledge and skills you’ll need to excel in these industries and explore related career pathways. 

Upcoming Courses

• Medical Device Process Validation
• Mobile Health, SaMD, and AI/ML Devices (starts before the info session)
• Risk Management for Regulated Industries
• Foundations in Medical Devices: Developing Premarket U.S. Regulatory Strategies and Working in a Regulated Environment
• Communicating and Negotiating with the FDA
• Good Manufacturing Practices
• Post-Market Regulatory Obligations for Medical Devices
• Regulatory Submissions: Devices and Diagnostics

This event is hosted by UCSC Silicon Valley Professional Education.