William T. Lee
Vice President
Regulatory Affairs
Cato Research
Israel
Biography
Dr. Lee has more than 25 years’ research and industrial experience in gene therapy, cellular immunology, and therapeutic vaccines, including 11 years in regulatory affairs. He has experience in the writing of patents and in the design and execution of preclinical studies, and he currently participates in the preparation and submission of various INDs, NDAs, and FDA meeting packages. Dr. Lee has experience in pharmacogenetics and the therapeutic areas of infectious diseases and oncology. Dr. Lee is regulatory affairs certified by the Regulatory Affairs Professionals Society. Dr. Lee has more than 25 years’ research and industrial experience in gene therapy, cellular immunology, and therapeutic vaccines, including 11 years in regulatory affairs. He has experience in the writing of patents and in the design and execution of preclinical studies, and he currently participates in the preparation and submission of various INDs, NDAs, and FDA meeting packages. Dr. Lee has experience in pharmacogenetics and the therapeutic areas of infectious diseases and oncology. Dr. Lee is regulatory affairs certified by the Regulatory Affairs Professionals Society.
Research Interest
Regulatory Affairs
