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November 9-11, 2020 | Virtual Conference
CAPT Kiester is a Division Director in the Office of Process and Regulatory Operations in OPQ. His division is responsible for managing the assessments of all Abbreviated New Drug Applications. He is a graduate of Duquesne University, with a Bachelor of Science in Pharmacy and a Master of Science in Health Science from Trident University. He started his career with the FDA and United States Public Health Service in 2001 when he came to the Office of Generic Drugs as a Chemistry Project Manager. In addition, he has held positions as a Regulatory Review officer and a Microbiology Project Manager within the Office of Generic Drugs. In addition he has served as a Branch Chief in the Office of Product Quality, for the project management staff responsible for the review of the quality portion of original ANDA’s.