Tony Horton has had a distinguished career in the pharmaceutical industry spanning more than thirty five years with such companies as BenVenue, Mylan Laboratories, Gensia Sicor Pharmaceuticals, Fujisawa and Baxter Labs. His extensive background includes hosting regulatory agency manufacturing site inspections with the FDA, EMEA, JP, MCA/MHRA, German Regulatory Agency, Australian Regulatory Agency, and ENVISA. Mr. Horton has led successful PAI’s and GMP re-certification inspections for more than fifteen products. His last fifteen years have focused on working with companies under regulatory stress. During that time, Mr. Horton guided companies through four consent decrees and one fraud policy, devising response plans and leading them through corrective actions and ultimate resolution. A highly regarded quality assurance expert, he has presented his work at several national and international scientific symposia and conferences. Mr. Horton is a graduate of Western Carolina University.