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Akosua’s experience involves working with life science companies on a wide range of FDA-related issues. Her practice focuses on product development and approval, clinical trials, and risk management, in addition to strategic FDA regulatory and compliance advice. Akosua’s advice in this area encompasses pharmacovigilance, Current Good Manufacturing Practice (cGMP), Good Clinical Practice (GCP), advertising and promotion, and Risk Evaluation and Mitigation Strategies (REMS). 

Credentials

  • The George Washington University Law School, 2021, J.D.
  • Wake Forest University, 2016, B.A., magna cum laude

  • District of Columbia

  • Food and Drug Law Institute (FDLI)