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Ms. Flint comes to Cato Research from EPIX Medical, Inc., where she was Vice President of Regulatory Affairs and Clinical Operations. Ms. Flint has more than 25 years of experience in regulatory submissions and clinical trials.
Ms. Flint previously held the position of Director of Clinical Trials at Advanced Magnetics, Inc. and Director of Regulatory Affairs at Du Pont Pharmaceutical Company. She has filed numerous applications for INDs and 10 NDAs, along with several medical device applications. Ms. Flint is certified by both the Regulatory Affairs Professional Society and the Association of Clinical Research Professionals. She received her MS in pharmacology from Northeastern University. | 