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Miah Jung

Miah Jung is a Pharmacologist in the Compliance Enforcement Branch, Office of Scientific Investigations, Center for Drug Evaluation and Research (CDER), FDA. She has been with FDA for six years, and serves as a subject matter expert in Good Clinical Practice (GCP) inspections to evaluate data integrity, quality, and subject safety in clinical studies for FDA’s Bioresearch Monitoring (BIMO) Program. Dr. Jung received her PharmD from University of Maryland and MS in biotechnology, regulatory affairs, from John Hopkins University. Prior to FDA, she has worked in academia coordinating clinical research studies.

My Speakers Sessions

Tuesday, June 25