Emily Andre

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, Emily has a robust background in regulatory submissions and collaborative project management. They earned their PhD in Neuroscience from the University of Virginia, where they focused on the huntingtin protein and its implications for health in Huntington’s disease models. Prior to their current role, Emily held various positions, including Regulatory Specialist at Technical Resources International, Inc., and Post Doctoral Fellow at Georgetown University Medical Center.