Robyn E. Shaw

Ms. Shaw has 20+ years of experience in the contract research industry with a broad perspective in research toxicology, immunology, and infectious diseases. She has extensive knowledge in preclinical studies in acute, subacute, and chronic toxicity in GLP environments. She also is knowledgeable of regulatory documents including The Guide for the Care and Use of Laboratory Animals, The Animal Welfare Act, Public Health Service Policies, the AVMA Guidelines, and the US FDA’s GLPs. Prior to joining Noble, she was the Director of Preclinical Services at Spring Valley Laboratories, Inc.