Keeping Medical Products Safe and Effective
The University of Washington's Master of Science in Biomedical Regulatory Affairs program trains professionals to manage the process of bringing new medical products to market. In this two-year, part-time or full-time program, you'll develop expertise in the regulations governing medical product development and learn how to lead every step of the regulatory process.
Faculty and alumni describe how the UW Master of Science in Biomedical Regulatory Affairs program prepares future leaders in the regulatory affairs field.
Launch or Advance Your Career
With a uniquely broad focus on drugs, devices and biologics, our program prepares you for roles in manufacturing, compliance, marketing, quality assurance and more.
Gain Practical Experience
During the program practicum, you’ll gain crucial on-the-job experience at a Seattle-area company or institution in the biotechnology, biomedical or medical device field.
Study While You Work
Courses meet in the evenings on the Seattle campus, so you can conveniently fit your studies around your work schedule.
Learn from Experts
Our instructors are regulatory affairs practitioners in the Seattle area. Get insights on how to be successful in this industry and grow your professional network.
"I feel my opportunities are a direct result of the education I received from the Master of Science in Biomedical Regulatory Affairs program."
— Ali Bouge
Quality and Regulatory Specialist, Stanford Department of Pediatrics, Stem Cell and Gene Therapy Clinical Trials Office