U.S. Food and Drug Administration
Mirette Mina is a postdoctoral fellow at the U.S. Food and Drug Administration, with a Doctor of Pharmacy degree from University of Maryland Eastern Shore. She completed an internship at FDA in the Office of Clinical Pharmacology prior to her fellowship. Her internship consisted of reviewing approved drug labels to explore the effect of food on drug absorption in pediatrics. She also participated in pediatric review committee meetings for discussion of product applications. Her fellowship is within the Office of Research and Standards under the Office of Generic Drugs. Her primary research focuses on global harmonization of bioequivalence criteria for narrow therapeutic index drugs. Other research includes global distribution of FDA regulated products and their manufacturing sites to support generic drug development. Her work has been presented internally at FDA. Furthermore, she is a member of the American Society for Clinical Pharmacology and Therapeutics.