Review of organisational structures in relation to Quality Management; design and rermediation of Quality Systems in the pharmaceutical arena to ensure regulatory compliance, business continuity and quality risk management; design and delivery of customised training courses to the pharmaceuticla sector in best practice standards and requirements; interpretation of legislative and best practice requirements and standards for the pharmaceutical industry.
Specialties: Development, evaluation and remediation of Quality Systems in all areas of the pharmaceutical arena (GMP, GDP, GLP, GCP etc); training in best practice standards in the pharmaceutical industry; interpretation and application o...
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complianceoperationseuropeexcipientrisk assesmentpharmaceuticalsgood manufacturing practicegdpsupply chainbiopharmaceuticalsintegritygmpgood distribution practice
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