Molly Follette Story, PhD is a Senior Advisor in Sanofi’s Medical Device Development Unit. She was formerly Senior Director of Sanofi’s Global Usability Engineering and Risk Management group. Before joining Sanofi, Dr. Story was Human Factors and Accessible Medical Technology Specialist at the U.S. Food and Drug Administration, Center for Devices and Radiological Health, Office of Device Evaluation, where she had an appointment to the Senior Biomedical Research Service. Dr. Story is an expert in human factors engineering of medical devices, with particular expertise in universal design of products and in the accessibility and usability of medical devices. 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 University of California, Berkeley.