Course Detail

GCP002A - Good Clinical Practice GCP Full course Split over two half days

This course is suitable for all new researchers conducting trials of a medicinal products (drug trials). If you have not previously attended a GCP course and you are currently or likely to be working on one or more Clinical Trials of Investigational Medicinal Products (CTIMPS/drug trials) then you are required to take the GCP (Full Course).

If you are expecting to be working on both CTIMP and non-CTIMP studies this is also the appropriate course for you, as it covers the general guidance and principles that apply to both types of research. However, if you are not expecting to work on any CTIMPs now or in the future, you may find the Research Governance Framework Course more applicable to your research.

All CTIMPs carried out in the UK are governed by the Medicines for Human Use (Clinical Trials) Regulations (Statutory Instrument 1031-2004). All staff working on CTIMP studies must be trained in the Principles of Good Clinical Practice and the Regulations and their application to research.
This course provides the attendee with an explanation of why Clinical Trials Regulations were introduced, a short description of the regulations and what constitutes Good Clinical Practice.
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.


Provided by: Joint Research Management Office


Day 1

Date: Thursday 7 March 2019

Venue: John Ellis Lecture Theatre, Dental Hospital Basement, Whitechapel

Time: 13:00 - 16:30

Day 2

Date: Friday 8 March 2019

Venue: Clark Kennedy Lec Theatre, W, Queen Mary Innovation Centre, Whitechapel

Time: 13:00 - 16:00


  • Mrs M Good