Areas of Expertise:
Nina M. LaValley, MSc
Nina LaValley is a clinical development and regulatory affairs professional, providing regulatory and technical support in the healthcare product industry. She assists in authoring clinical documents, such as Clinical Study Reports, Investigator Brochures, protocols, and electronic common technical document sections required for INDs and NDAs. She also processes, publishes, and performs quality control review of electronic regulatory submissions for filing to the U.S. Food and Drug Administration (FDA). Nina has prepared client-specific standard operating procedures according to regulations, guidelines, and appropriate stage of drug development. Nina has a B.S. in Biology from the College of William and Mary and an MSc in Biomedical Sciences from Wake Forest University.