The remit of the NREC-CTs is to review the submission of ethics applications related to Clinical Trials of Investigational Medicinal Products (CTIMP). This includes interventional studies and low-interventional studies involving medicinal products for human use.
Two NREC-CTs will run in parallel – NREC-CT A and NREC-CT B – with each committee meeting monthly.
The NREC-CTs will initially run concurrently with many local recognised RECs to review CTIMP ethics applications for a defined transition period. This approach will collectively support this important area of research and ensure a smooth transition ahead of the EU Clinical Trial Regulation.
For further information related to the NREC-CT, please contact the National Office – firstname.lastname@example.org
If you plan to submit a CTIMP application for ethics review, please visit Apply NREC-CT.
If you are interested in the underlying processes and management of the NREC-CT, please download our Operational Framework.