Bev Dixon joined Contineum Therapeutics as a consultant in 2020 and as a full time employee in September 2023. As the Senior Director of Quality Assurance, she brings a broad range of Quality experience covering GMP, GCP and GLP areas. Her experience in this capacity comes primarily from her role as Director of Quality/Regulatory Affairs at Molecular Biosystems in San Diego, CA and subsequently as a consultant for a diverse group of small and large pharmaceutical companies requiring her expertise in Quality Management. She has supported non clinical and clinical development and approval of products in the United States, Canada, Mexico and a consolidated approval in the European Union. As a consultant, she has worked with primarily early-stage companies who were developing and sustaining their respective products with the support of an effective Quality Management System, appropriate for their stage of development. Her areas of expertise include Computer Science, Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs, Validation, Document Control, Quality Control and Quality Assurance. She holds a bachelor’s degree in Psychology from the University of Delaware and a Masters of Science Degree in Quality Assurance from California State University, Dominguez Hills.