Executive Director, NSF
Rachel has 30 years’ experience of pharmaceutical manufacture and quality management including nearly 11 years as a GMDP Inspector for the UK Competent Authority, the MHRA.
Rachel has wide ranging experience of inspecting against European Good Distribution Practice and Good Manufacturing Practice requirements in the UK, China, India and the US meeting the associated quality standards for medicines (non-sterile and aseptic production, including radio pharmaceuticals) and the blood industry. She delivers training, auditing and consultancy.
Rachel is Biochemist with a Masters degree in Industrial Pharmaceutical Studies, taken as part of her Qualified Person training and is a member of the Royal Society of Biology.