After training as a pharmacist, Mary’s first role was in clinical trial supplies at British Biotech where she set up a new clinical trials packaging and labelling department which managed the packaging and labelling and supply of investigational medicinal products for the company. These included phase I to phase III clinical studies.
Mary moved into GCP compliance at British Biotech in December 1997. Her experience extended to conducting various clinical audits including site, database, clinical study report and system audits. She also developed GCP and SOP training programmes for the clinical team. Her role as QA Manager also encompassed development and implementation of quality management systems, in accordance with GMP, GLP and GCP requirements.
Over the past 10 years, Pharma-QA has provided QA consultancy services globally for a wide range of pharmaceutical companies, including many of the services detailed on this website.
A full range of references are available, upon request.
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