Training
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Training
We can provide training in order to aid you in running a research project.
We run the following courses:
- Good Clinical Practice (GCP) Full and Refresher training*
- Valid Informed consent training
- Investigator Site File set-up and maintenance
Other training is also available from the following resources:
- Health Research Authority (HRA) e-learning
- Learn NIHR (National Institute for Health Research)
- Standard Operating Procedures (SOPs)
- Medical Research Council (MRC)
*Note: It is mandatory to have GCP Training if you are a member of a research team conducting a Clinical Trial of Investigational Medicinal Product (CTIMP) or a medical device trial. GCP training needs to be renewed every 2 years by attending a ‘refresher’ course.