Mr. Stock offers more than 27 years of process/operations and compliance experience in the pharmaceutical, biotech, and medical device industries. He has successfully started-up, commissioned and validated cell culture facilities, vaccine facilities, oral solids and liquids facilities, bulk chemical and medical device facilities. Mr. Stock has developed and presented training programs and seminars for cGMPs, Contamination Control, Commissioning and Validation, Project Management and Master Planning to U.S. and international industry groups (ISPE, PDA, Institute for Validation Technology,Pharmaceutical Sciences Group, Medical Device Manufacturers and the Center for Professional Advancement) and to individual companies.

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