معرفی
Lynn Rose serves as an Affiliate Assistant Professor in the MS in Biomedical Regulatory Affairs (BRAMS) Program at the University of Washington School of Pharmacy and is a founding member of the UW Institute of Translational Health Sciences' Drug and Device Advisory Committee, advising academic investigators on regulatory requirements for biomedical product development.
Her educational background includes:
- PhD in Immunology from the University of Geneva, Switzerland
Dr. Rose possesses extensive expertise in regulatory strategy, clinical protocol design, and federal regulatory submissions, with deep research roots in immunology spanning autoimmunity, infectious disease, and immune-oncology. Her industry experience includes leading drug development teams that produced marketed therapies for cystic fibrosis and hemostasis, directly informing her academic focus on bridging translational research with regulatory pathways.
She teaches PHRMRA 536 (Skills for the Regulatory Affairs Professional) and PHRMRA 548 (Practicum), while her advisory role in the Drug and Device Committee provides critical guidance to researchers navigating complex FDA/EMA requirements for novel biomedical products.
