Priscilla Roy

Priscilla Roy possesses extensive experience in regulatory affairs and quality control within the pharmaceutical and biotechnological sectors. Currently serving as the Regulatory Affairs Deputy Manager at Inovet since August 2012, Priscilla has been involved in CMC writing for new generic and hybrid product dossiers. Previous roles at Inovet include Regulatory Affairs Coordinator, Regulatory Affairs Assistant, and Stability Studies Technician, where responsibilities encompassed stability testing, analysis coordination, and data interpretation. Before joining Inovet, Priscilla worked as a Quality Control Technician at MINAKEM and Bio-Rad Laboratories, focusing on the quality control of raw materials, semi-finished, and finished products while adhering to GMP standards. Priscilla's academic background includes a Licence in Organic Chemistry from Pierre and Marie Curie University and a DUT in Chemistry from the University of Lille 1 Sciences and Technology.