Patricia Brown is Vice President of Regulatory Affairs and Quality Assurance with over 30 years’ experience as a quality and regulatory professional in the pharmaceutical, biologics, medical device, and combination product industries. She spent the early part of her career working as a Consumer Safety Officer specializing in the pharmaceutical industry for the United States Food and Drug Administration. After 6 years with the FDA Patricia worked in regulated industry for various start-up and small companies including Eyetech Pharmaceuticals, Agilent Technologies Nuceleic Acid Solutions Division, Clovis Oncology, Array Biopharma, ArcherDx, and Aktiv Pharma Group building Quality Management Systems along with quality and regulatory teams. Patricia has successfully been part of management teams that have released clinical products and launched commercial products in the United States, Canada, European Union, United Kingdom, and Japan. Patricia joined VitriVax in January 2025 as the quality and regulatory lead tasked with developing phase-appropriate GMP and GLP infrastructures and regulatory processes.  She earned her BS in Microbiology from the University of Illinois, Urbana-Champaign.