Emily Andre, PhD, RAC, is the Associate Director of Neurology Regulatory Affairs at MCRA, an IQVIA Business, where they develop and execute regulatory services for medical devices and biologics. With 13 years of experience, they have a strong background in regulatory submissions and effective communication across cross-functional teams. Emily earned a PhD in Neuroscience from the University of Virginia and has held various positions in regulatory affairs and research, including roles at Technical Resources International, Inc. and Georgetown University Medical Center. Prior to their current role, they served as Manager and Senior Associate in Neurology Regulatory Affairs at MCRA, developing regulatory submissions and ensuring compliance with FDA regulations.
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