How CNTW can support researchers
All research studies being conducted at CNTW need regulatory approvals. Different types of studies need approval from different regulatory bodies:
Health Research Authority (HRA)
Every research study taking place in the NHS in England and Wales, where service users, carers, or staff are taking part, needs HRA approval. That includes all research at CNTW, except some types of student research.
Research Ethics Committee (REC)
When a research project involves NHS participants, it must be approved by a Research Ethics Committee. These committees are entirely independent of sponsors, funders and people doing the study. This enables them to put participants at the centre of their review.
Confidentiality Advisory Group (CAG)
The Confidentiality Advisory Group (CAG) is an independent body. It provides expert advice on using confidential patient information appropriately. CAG protects and promotes the interests of patients and the public.
Medicines and Healthcare products Regulatory Agency (MHRA)
If your project is a Clinical Trial of an Investigational Medicinal Product (CTIMP) it will need Clinical Trial Authorisation from the MHRA. Use the MHRA’s algorithm to see if your project is a CTIMP.