Area of Expertise:
Sara Price, MA
Sara provides technical, scientific, and regulatory support for pharmacology, pharmacokinetics, and toxicology studies, as well as strategic nonclinical development support for drugs, biologics, and combination products/devices for a variety of indications, including cardiovascular, renal, medical imaging, and neurology. She has experience in outsourcing support including study monitoring, nonclinical project management, conducting gaps analysis, and authoring development plans. Sara also lends her expertise in scientific authoring, reviewing, and management of nonclinical regulatory submissions including INDs, NDAs, BLAs, nonclinical study waiver requests, special protocol assessments, meeting requests, and briefing packages, as well as participation in meetings with regulatory agencies. She also has expertise in impurity, excipient, metabolite, and chemical safety assessments using industry standard approaches, Standard for Exchange of Nonclinical Data (SEND) submission requirements, and authoring product safety data sheets. Prior to joining SciLucent, Sara conducted behavioral research with animal models and worked in the field of research compliance and ethics. Sara has a B.S. in Neuroscience/Behavioral Biology from Emory University and an M.A. in Cognitive Sciences from Georgia State University. Sara is an active member of the American College of Toxicology and Society of Toxicology.