Keeping Medical Products Safe and Effective
The University of Washington's Master of Science in Biomedical Regulatory Affairs 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.
Prepare for Diverse Career Opportunities
The Master of Science in Biomedical Regulatory Affairs (BRAMS) is geared to those who want to launch or advance their career in the regulatory affairs field. With a uniquely broad focus on drugs, devices and biologics, our program prepares you for roles in manufacturing, compliance, marketing, quality assurance and more.
Explore Careers Gain Practical Experience
Students benefit from the program's close ties to the Seattle-area biotechnology, medical device and biomedical industries. During the program practicum, you’ll gain crucial on-the-job experience in regulatory affairs at a Seattle-area company or institution.
Learn About Practicum Take Convenient Evening Classes
We designed the Master of Science in Biomedical Regulatory Affairs program with working professionals in mind. In the part-time option, all courses meet in the evenings on the Seattle campus, so you can conveniently fit your studies around your work schedule.
"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
UW BRAMS Graduate
Quality and Regulatory Specialist, Stanford Department of Pediatrics, Stem Cell and Gene Therapy Clinical Trials Office
Read Ali's story