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Rebecca Stanbrook | Speaker | Fleming
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Rebecca Stanbrook

GCP Expert
Switzerland
Rebecca Stanbrook BPharm (hons), MRPharmS, FFRPS, DipRQA, FRQA
Rebecca Stanbrook has worked in the pharmaceutical industry, as a regulator at the MHRA and at various pharmaceutical companies for over 30 years. For 11 years she worked at the MHRA, latterly as Group Manager, Inspections, GCP, GLP and Pharmacovigilance. Her group was responsible for writing the Good Clinical Practice Guide, aka the Grey Guide,
She is a pharmacist by profession and holds a Diploma in Research Quality Assurance.
Rebecca is thrilled to be a member of the ICH E6(R3) Expert Working Group.

Events/Masterclasses Rebecca Stanbrook is currently speaking at

Pharma

Digital Quality in Clinical Trials
22 – 23 April 2026
Vienna, Austria
With the increasing complexity of today’s clinical trials, as well as the speed of technological innovation and AI tools utilization, unique issues remain especially around clinical trials and the use of electronic systems.
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Rebecca Stanbrook
GCP Expert
Switzerland
Rebecca Stanbrook BPharm (hons), MRPharmS, FFRPS, DipRQA, FRQA
Rebecca Stanbrook has worked in the pharmaceutical industry, as a regulator at the MHRA and at various pharmaceutical companies for over 30 years. For 11 years she worked at the MHRA, latterly as Group Manager, Inspections, GCP, GLP and Pharmacovigilance. Her group was responsible for writing the Good Clinical Practice Guide, aka the Grey Guide,
She is a pharmacist by profession and holds a Diploma in Research Quality Assurance.
Rebecca is thrilled to be a member of the ICH E6(R3) Expert Working Group.
Rebecca Stanbrook
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