Suzanne Thornton-Jones has a Ph.D. in Pharmacology and Toxicology from the Medical College of Virginia/Virginia Commonwealth University. In her current role GTP, she leads the Global Regulatory Affairs department who are responsible for developing the global regulatory strategy including engagement of Health Authorities throughout the nonclinical research, clinical trial, and registration processes.  In addition to her regulatory responsibilities, she also leads the Compliance group, Good Laboratory Practice (GLP) Quality Assurance Unit, which is responsible for auditing nonclinical studies used to support Health Authority regulatory filings.