DON'T USE - SUPERSEDED - Inspection Survival Guide: Being Prepared for an MHRA GCP Inspection

About

Statutory GCP inspections conducted by the Medicines and Healthcare products Regulatory Agency (MHRA) are an important part of the regulation of clinical trials in the UK. Anyone who sponsors, conducts or supports a clinical trial in humans involving an investigational medicinal product (cTIMP) or a medical device may find themselves face-to-face with an MHRA inspector. What an inspector will be looking for is evidence that trials have been conducted in compliance with applicable legislation and the principles of GCP. It is a daunting prospect for many, but an understanding of what to expect and how to prepare can help smooth the process and lead to a successful inspection outcome.

Tutor

James Gibson

Cost

  • Student = £40 (matriculation details required)
  • University of Edinburgh/NHS Lothian = £60
  • Other academic/NHS - £90

For industry rates, email education@edinburghcrf.ed.ac.uk.

There is a cancellation date of 02 November 2022. You will be charged if you cancel after this date.

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