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Overview

Alison Mulry focuses her practice on FDA regulatory, compliance and legal matters affecting pharmaceutical, biotechnology, and medical device companies. She provides counseling on business decisions spanning the entire pharmaceutical product life cycle, from research and development to product launch and commercialization.

Prior to beginning her regulatory practice, Ali gained significant experience handling patent litigation matters for branded pharmaceutical clients.

Education

  • Indiana University, B.S., Neuroscience, with High Distinction.
  • University of Virginia School of Law, J.D., Editorial Board, Technology Editor, Virginia Journal of Law and Technology

Bar Admissions

  • New York