Getting started
Good clinical practice (GCP)
GCP is the agreed international standard for conducting clinical research.
Good Clinical Practice Training is required for researchers conducting Clinical Trials of Investigational Medicinal Products (CTIMPs). It ensures that the rights, safety, and wellbeing of trial participants are protected, and that the data generated is credible and reliable.
Everyone who works on delivering Clinical Trials of Investigational Medicinal Products (CTIMP) has to have an up-to-date GCP certificate.
Early Vasopressor in Sepsis (EVIS)
To be authorised to confirm eligibility and prescribe for the EVIS study, read the three slide-sets below and hold a current GCP certificate. Then email the ED Research Team to sign the delegation log.
CURLY
To confirm eligibility and prescribe for the Curly trial, review the two short slide-sets below, then email the Research Team to arrange being added to the delegation log.
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uDCD – Uncontrolled Donation After Circulatory Death
A feasibility study of uncontrolled donation after circulatory death. Complete the training presentation linked below, then email the Research Team to be added to the delegation log.
ASPECT – Aspirin in Pneumonia
Aspirin in patients with pneumonia for the prevention of cardiovascular events. A doctor must prescribe, but GCP is not required for this study. Training modules are on the ED SharePoint folder — your device must be logged into your nhs.net account to access them.
After completing the modules, follow the link in the folder to register on the online delegation log.
Contact the Team
The EuReCa team work Mon–Fri, 09:00–17:00. Once you've completed your training, get in touch to arrange signing the delegation log.