Ian has 22 years experience in all aspects of Quality Control and Quality Assurance for oral, solid dosage forms, powder dosage forms and non-sterile liquids, with experience in QC/QA aspects of formulation and development projects from phase I clinical supplies through to scale-up for commercial operations, as well as the monitoring of commercial operations.
Ian has been involved in the initiation and management of commercial importation projects for a range of sterile and non-sterile pharmaceutical dosage forms. He has advised clients in the EU requirements for QP certification of imported products, and has been an active participant in project teams involved in the launch of commercial imported products onto the EU market.
Ian has led the Almac Pharma Services audit team in EU and US regulatory inspections and routine customer audits. He is named on Almac Pharma Services Manufacturers Importers Authorisation as responsible for Quality Control on site, and has been a Qualified Person responsible for the release of batches to market, for the last twelve years.