Join us for our upcoming information meeting and get details on course curriculum, time commitments and more. Plus, a program rep will be on hand to answer any questions.
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This Info Meeting is For:
Learn about the role of a biomedical products regulatory affairs specialist and the dynamic nature of the field. Explore the regulatory jurisdiction of the U.S. Food and Drug Administration.
Develop a thorough understanding of the fundamental concepts and principles that guide the design and implementation of different types of clinical trials.
Learn the key aspects of taking a medical product — drug, device or biologic — from concept to market, including clinical trials and post-marketing surveillance.
To request disability accommodations, please contact the UW Disability Services Office as soon as possible at 206-543-6450 or firstname.lastname@example.org.
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