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Judith Jones

Principal Consultant, Pharmacovigilance, Epidemiology, and Risk Management
Dr. Jones is a clinical pharmacologist/pharmacoepidemiologist trained in geriatrics and internal medicine with a longstanding interest in the study of adverse drug reactions, drug utilization, and drug development and regulation. She received her medical training at Baylor College of Medicine, followed by clinical training in internal medicine, a fellowship in clinical pharmacology, and a Ph.D. in developmental pharmacology at University of California, San Francisco. She was head of Postmarketing Drug Safety at FDA from 1978-85, then founded The Degge Group, Ltd. in 1988 to provide Safety consulting and epidemiology studies. In 2018 she sold this group to Pharmalex, LLC USA & is a consultant with them. She serves on a CIOMS & USAN panel.