MHRA Inspection - Training Seminars
Good Clinical Practice (GCP) Training
All researchers involved in a Clinical Trial of an Investigational Medicinal Product (CTIMP), i.e. a study which falls under the Medicines for Human Use (Clinical Trials) Regulations 2004, are legally obliged to conduct their research study in compliance with Good Clinical Practice (GCP).
It is a requirement that all members of a trial team identified on the Trial Delegation Log, not just the Chief Investigator/ Principal Investigator (CI)/ (PI), complete GCP training. GCP training should be renewed every two years.
CRC Cymru is one organisation that provides courses on GCP training. Please click here for a list of CRC Cymru training opportunities and dates.
GCP training is also available from other providers. When available, dates will be displayed below:
Cardiff and Vale NHS Trust Research and Development Office has organised three half day sessions for Clinical Researchers who require Good Clinical Practice and the EU Clinical Trails Directive training:
28th May 08:45 - 13:00
28th September 13:30 - 17:00
3rd December 08:45 - 13:00
Registration forms are available from Cardiff and Vale NHS Trust R&D Office:
Ground Floor, Radnor House
University Hospital of Wales
Cardiff, CF14 4XW
Tel: 029 2074 6986
Fax: 029 2074 5311
Online GCP training can be found at the following websites: