Resources

Information for research participants

If you are thinking about participating in a PRIMENT CTU study, or are already part of a study, you can find general information about taking part in research studies and PRIMENT CTU here: Priment CTU & research studies

Resources for researchers

PRIMENT CTU has developed a wide range of Standard Operating Procedures (SOPs) to guide chief investigators and other research staff through the process of conducting a successful trial. 

The following groups and organisations may be helpful resources for those interested in conducting a clinical trial. PRIMENT CTU assumes no responsibility for the content of these sites.

UCL Resources

• Institute of Clinical Trials and Methodology
• Research Department of Primary Care and Population Health (PCPH)
• Division of Psychiatry
• Department of Statistical Sciences
• Data Safe Haven

Research networks

• NIHR Mental Health Research Network
• NIHR Primary Care Research Network

Funding bodies

• NIHR Central Commissioning Facility
• Medical Research Council (MRC)

The Research Design Service (RDS London) supports researchers in developing and designing research proposals for submission to NIHR and other national, peer-reviewed funding competitions for applied health or social care research.

UK Regulatory Information

• The UK Clinical Research Collaboration (UKCRC)
• MHRA Good Clinical Practice (GCP)
• UK Research Governance Framework for health and social care
• EudraCT (European database of ongoing and completed clinical trials)