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Sandra Milligan, MD, JD, currently serves as Vice President, Global Regulatory Affairs, Therapeutic Area Head for Inflammation, Infectious Disease and Ophthalmology for Genentech/Roche where she develops and directs global strategic regulatory plans to facilitate and optimize product development, regulatory approval, and commercialization. She previously served at Amgen for 10 years in various roles, including Global Regulatory Therapeutic Area Head for the Bone franchise, as Head of Regulatory Communications Strategy & Operations, and as Senior Counsel, for the Development, Regulatory & Compliance Law Group, where she provided legal strategy for development, regulatory and safety groups. In addition to serving on the DIA Board of Directors, Sandra has served as the Chair of the 2013 DIA Annual Meeting (Boston), as DIA Annual Meeting session chair and as co-chair of the Public Policy/Health Care Compliance/Regulatory Law Annual Meeting track. Sandra is a graduate of The George Washington University School of Medicine and Health Sciences, and of the Georgetown University Law Center.