Sarah Tanveer, PhD

Sarah Tanveer is a Postdoctoral Research Fellow with PORTAL. Her research focuses on issues related to FDA decision-making, assessment of benefits and harms of pharmaceutical products, and evidence synthesis methodology.

Sarah completed her PhD in Pharmaceutical Health Services Research at the University of Maryland, Baltimore, and her MA from Johns Hopkins Bloomberg School of Public Health. Her dissertation focused on the causality assessment of adverse drug events. Sarah served as an ORISE fellow at the FDA’s Center for Drug Evaluation and Research where she contributed to high-priority research topics for both the Office of Surveillance and Epidemiology and the Office of New Drugs. Sarah also completed a postdoctoral fellowship with the Meta-Research Innovation Center at Stanford (METRICS) prior to joining PORTAL.