Daniel Krietlow, MA

Dan provides technical, regulatory, and strategic support in pharmacology and toxicology activities. His experience in nonclinical safety and development allows him to review, analyze, and interpret study reports and author nonclinical sections for regulatory submission. Dan has significant experience as a Study Director in contract research organizations and has conducted a large number of nonclinical safety studies in different species, using multiple routes of administration for a wide variety of pharmaceutical and biologic agents. Dan provides expert services for the planning, conduct, monitoring, and reporting of nonclinical studies to ensure that they are performed as per current industry standards, GLP and animal welfare regulations. He also serves as a contributing author of nonclinical sections of documents intended for submission to regulatory authorities. Dan has an M.A. in Educational Leadership from the University of Nevada.