Dr. Harrington is a Principal Consultant with DPS based in Ireland, who has been working in the Pharmaceutical Industry since 1992. Aidan has worked in QA, Validation and Engineering roles in both manufacturing and capital project environments for the pharmaceutical industry and is an expert in US FDA and EU cGMP regulations. He has extensive regulatory inspection exposure experience; EMA, FDA and HPRA. Aidan has played significant roles on the planning and implementation of Commissioning and Qualification programs for large capital projects including implementation of Quality Risk Management principles from concept design phases to product Process Validation for sterile and biologics drug substance manufacturing facilities. Aidan offers consultancy to a range of clients in areas such as concept design for cGMP compliance, risk reviews, inspection pre-audits, technology transfers, new technology assessments and contamination investigations.