With over 25 years’ experience in the pharmaceutical industry, Ian is responsible for Quality Assurance and Laboratory operations for Almac Pharma Services across all sites, and achieved Qualified Person status in 1999. He has led the global audit teams in the management of regulatory inspections by EU, U.S. and multiple ROW regulatory authorities. Involved in the initiation and management of commercial importation projects for a range of sterile and non-sterile pharmaceutical dosage forms, Ian advises global clients in EU requirements for QP certification of imported products.
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