Megan DoyleDirector, Global Regulatory and R&D Policy at Amgen
Megan Doyle is an attorney and policy professional with nearly 15 years of experience in the regulation of drugs, medical devices, combination products, and in vitro diagnostics. She received her law degree from Georgetown University Law Center and her master’s degree in public health from Johns Hopkins University. After seven years in the medical device practice at Hogan Lovells, she joined Amgen as a Senior Counsel for Health Regulatory. For four years, she counseled Amgen on drug, device, combination product, digital health, and diagnostic matters. She also advised on the co-development process for teams developing targeted therapies that require a companion diagnostic. Currently, she is a Director in Amgen’s Global Regulatory and R&D Policy group, where she is the Global Policy Lead for Diagnostics, Digital Health, and Oncology.