Marianne Frost

SVP, Regulatory Affairs at Biohaven Pharmaceuticals

Ms. Frost has over 20 years of drug development experience with 18 years in various roles within Regulatory Affairs. She joined Biohaven after 11 years at Bristol-Myers Squibb, 5 years at CuraGen Corporation, and 5 years at Wyeth working in the therapeutic areas of neuroscience, virology, immunology, oncology and women’s health. Her experience spans all phases of drug development from preclinical research through Phases 3 and marketed products. Her numerous successful health authority interactions globally include approval of a new drug application for Daklinza and several Abilify sNDAs in the U.S. Ms. Frost has a B.A. in psychology from Northeastern University and a M.A. in behavioral neuroscience from the University of Connecticut.

Timeline

  • SVP, Regulatory Affairs

    Current role

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