United States Nuclear Regulatory Commission - Protecting People and the Environment

Molly Follette Story

Molly Follette Story, PhD is Human Factors and Accessible Medical Technology Specialist at the U.S. Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of Device Evaluation (ODE), where she has an appointment to the Senior Biomedical Research Service. Previously, she served as a Senior Program Officer at the National Research Council of The National Academies. Before that she was Principal of Human Spectrum Design and Co-Director of the Rehabilitation Engineering Research Center on Accessible Medical Instrumentation. Dr. Story is an expert in universal design of products and in the accessibility and usability of medical instrumentation, has been granted six utility patents, and has served as a research and design consultant to a variety of companies. Dr. Story received a BSE from Princeton University, a MS from Stanford University, and a MS and a PhD from the School of Public Health at the University of California, Berkeley.

Page Last Reviewed/Updated Wednesday, April 16, 2014