Institute of Clinical Research (ICR) has won the contract to provide Good Clinical Practice (GCP) training for experienced staff working on the UK Clinical Research Network (UKCRN) portfolio of trials
In July 2005, the UKCRN launched its training and education programme for members of the clinical research team working on the UKCRN portfolio of trials.
Among other modules, the training programme incorporates courses which introduce staff to the principles of good clinical practice.
ICR won the contract following a competitive tendering process from suitably qualified organisations and individuals and the courses will now be run at a range of locations from the second half of 2006.
Martin Robinson, principal training consultant at ICR said: "This is great news for the ICR and further recognition of our ability to deliver quality training.
"The Institute is firmly committed to the provision of training opportunities for clinical researchers to complement their professional development and provides a wide range of cost effective training courses relevant to all aspects of clinical research, both as open and in-company courses".
The course provides a practical insight into the history and application of regulations within clinical research and is delivered via a blend of trainer input, group discussions and practical workshops.
Course content includes an outline of the history and purpose of GCP, roles and responsibilities in clinical research, essential documentation, the EU Directives and GCP in action.
All new clinical research personnel will find the course of immense benefit and will also receive a copy of the International Conference on Harmonisation (IHF) GCP guidelines and the EU Directives on Clinical Trials and GCP.
The latest announcement is a further addition to ICR's suite of training programmes which through its collaboration with Cranfield University offers members post-graduate certificates, diplomas, masters of science degrees and PhDs in clinical research and its own certificate and diploma exam.
