Course Detail

GCP001 - Good Clinical Practice for Labs

This course will refresh and update the knowledge of those working on Clinical Trials of Medicinal Producsts (CTIMPs/drug trials) of Good Clinical Practice and Clinical Trial Regulations and how to apply in their role. This course is available for at staff who work for Queen Mary’s University of London and Barts Health NHS Trust, and who will not be charged . Delegates must register before the course and will be issued a certificate upon completion of the course.

For those who are working on Clinical Trial of Medicinal Products (CTIMPs/drug trials) who have previously attended GCP training but need to refresh and update their knowledge, then they are required to take this GCP Refresher Course. TThis course is mandatory for all researchers working on CTIMPs every two years.

The course will refresh clinical trial research staff’s knowledge of:

- Clinical Trial Regulations and Amendments
- The Requirements to comply with the Protocol, Agreements and Approvals
- Informed Consent
- Compliance with the Data Protection Act and Human Tissue Act
- Safety Reporting
- Maintaining Essential Documents
- Maintaining Data quality
- Reporting requirements
- Lessons learnt from MHRA inspections


Provided by: Joint Research Management Office


Date: Tuesday 18 June 2019

Venue: Scape 1.04, Scape, Mile End

Time: 09:30 - 14:00


  • Mrs M Good