Chrissy J. Cochran, PhD is Director of the Office of Bioresearch Monitoring Operations at the FDA, and is responsible for working with each of FDA’s product centers to establish and manage the BIMO program. She previously led the Division of Enforcement and Postmarketing Safety in CDER, led the good laboratory practice compliance program in CDRH, monitored clinical trials at a large clinical research organization, and performed laboratory research at the Veteran’s Administration. Dr. Cochran has a PhD and Masters of Science in Toxicology, and a Bachelor of Science in Biochemistry.