Jerome Bressi, Ph.D., is Senior Vice President of Regulatory Affairs & Quality at Fate Therapeutics, overseeing all aspects of regulatory and quality functions related to clinical development, CMC, and future commercialization. Previously, Dr. Bressi held the positions of Vice President of Regulatory Affairs & Quality and Executive Director of Regulatory Affairs at Fate Therapeutics. Prior to joining Fate, he served as President of BioPharma Regulatory Solutions, as well as played key regulatory roles at Hyperion Therapeutics and Mast Therapeutics. Dr. Bressi has more than 20 years of biotechnology and pharmaceutical industry experience in drug development within oncology, autoimmune, and inherited genetic disorder therapeutic arenas. He received his Ph.D. from the Department of Chemistry at the University of Washington and his B.S. from the Department of Chemistry at the University of California, San Diego.