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.