Mr. Purdue is a Registered Quality Assurance Professional in GLPs (RQAP-GLP) and has over 25 years of experience in performing GLP audits of facilities and studies to comply with U.S. FDA, EPA, European, and Japanese GLP regulations. He has 10 years’ experience in GMP Quality Assurance production of active pharmaceutical ingredients (APIs), kilo lab to small pilot plant scale. He also has cGMP experience in solid oral dosage manufacturing, lead QA experience in process change control, deviation and OOS resolution and CAPA reporting. Mr. Purdue has a Bachelor of Science in Chemistry from Wright State University. He is 28 year member of SQA and a member in GLP, GMP, and Scientific Archiving specialty sections. Mr. Purdue is currently a QA Compliance Analyst V in the Quality & Records Management group for Boehringer Ingelheim Pharmaceuticals Inc. at their U.S. Research and Development facility located in Ridgefield Connecticut.