How CNTW can support researchers
Regulatory approvals are required for all research studies being conducted within CNTW. Different types of studies will need approval from different regulatory bodies:
Health Research Authority (HRA)
Every research study taking place in the NHS in England and Wales, where participants are service users, carers, or staff, 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 research sponsors, funders and investigators. 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 which provides expert advice on the use of confidential patient information. CAG protects and promotes the interests of patients and the public, while facilitating appropriate use of confidential patient information for research.
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.