Pharmaceutical product development
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Lesley Chaplin

She has recently been Compliance Manager and Quality Assurance Manager at Antisoma Research where she implemented and managed the Quality Management System, GXP training plans, audit programmes and key performance indicators (KPIs) drawing on her practical application of Lean Six Sigma methodology and common sense. Lesley is a GMP Compliance auditor with a wide variety of global experience in Active Pharmaceutical Ingredient (API), Investigational Medicinal Product (IMP) and Clinical Supplies manufacturing sites. She is currently co-director of in2phase Limited a multi-disciplinary biotech consultancy group which specializes in supporting small biotech companies covering the areas of regulatory, QA, CMC, medical/PCV, and biometrics consulting.