About me
Rhonda Hearns-Stewart, MD, is a Senior Physician. She joined the FDA as a Medical Officer in the Office of New Drugs (OND) within the Center for Drug Evaluation and Research (CDER) in 2013. As a senior clinical reviewer in the Division of Bone, Reproductive, and Urologic Products (DBRUP), Dr. Hearns-Stewart was responsible for reviewing the majority of Assisted Reproductive Technology (ART) and infertility products. In 2017, she joined the Drug Trials Snapshot Team in the Division of Professional Affairs and Stakeholder Engagement (PASE) within CDER’s Office of the Center Director. In 2019, Dr. Hearns-Stewart joined the OND Immediate Office as the Associate Director of Implementation for the Integrated Assessment of Marketing Applications.
