This course covers all of the information required for those who will be conducting research in a clinical laboratory or setting-up, overseeing or managing the analysis of clinical samples as part of clinical research.

During this two and a half hour course, delegates will be asked to consider the key principles of GCP and how quality systems can be developed and maintained to ensure that the rights, safety and wellbeing of clinical trial subjects are protected and that data is reliably and accurately reported.

By the end of this course you will:

  • Know what GCP is and how it applies to you
  • Understand the regulations which apply to clinical trials
  • Understand the requirements of study setup and oversight
  • Be familiar with trial documentation
  • Be aware of key requirements of GCP including subject safety, confidentiality and consent
  • Be aware of important aspects of study conduct
  • Understand what an MHRA inspector will look for when visiting a lab

Event Details

2 September 2025, 10:00am to 12:30pm

Via Teams

  • KCL Event
  • GSTT Event