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Brian Kaufman

Vice President, Quality And Regulatory

Mr. Kaufman has over 25 years of experience with translational product development from preclinical to IND, clinical phase progression, regulatory submissions for approval and commercial products.  His background includes a breadth of regulatory, GxP quality, CMC, clinical and nonclinical roles coupled with sales and marketing compliance responsibilities.  He has worked on NIAID funded programs and served as Chief Compliance Officer for public company Sarbanes-Oxley requirements.  His expertise has been applied to product development with U.S. and international corporate partners involving global clinical sites, CROs, CMOs and GxP quality matters to achieve business goals and contributing to successful regulatory submissions.