Bio

Kevin has over 40 years of FDA regulated industry experience that includes management positions at Wyeth and McNeil Pharmaceutical. He is considered a subject matter expert on risk-based systems validation conducted within QA, IT, Manufacturing, Operations, Clinical and R&D in FDA regulated environments. He was a member of the PhRMA Computer Systems Validation Sub-Committee, was the Core Team Secretary for the PDA Part 11 Task Group, former co-chair of GAMP Global, and was previously a chair on the GAMP Americas Steering Committee. He received his Bachelor's degree in Chemistry from Delaware Valley College of Science and Agriculture, and his Master's of Engineering from Penn State University.