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Tina Kiang, PhD
Division Director, CDER
U.S. Food and Drug Administration
Tina Kiang, Ph.D. currently serves as the Director of the Division of Regulation and Guidance in the Office of Policy for Pharmaceutical Quality in the Office of Pharmaceutical Quality in CDER/FDA. She has over 20 years of combined regulatory and leadership experience at the FDA. Tina spent over 16 years in the Center for Devices and Radiological Health as a medical device reviewer and leader. In her current role, Tina has led and supervised the development and finalization of guidance and regulations on a variety of topics within pharmaceutical and manufacturing quality, including for novel areas such as advanced manufacturing and platform technologies. She received her Bachelor of Engineering in chemical engineering from The Cooper Union in New York and her Ph.D. in Biomedical Engineering from The Johns Hopkins University School of Medicine.
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