Before the submission to IRAS for the relevant ethical and regulatory approvals, it is important to initiate the internal approvals process for teams that will be involved in the study. Some teams will have fed into the feasibility assessment, but they may not yet be aware that the study is to go ahead.
Depending on the nature of your study, the teams to contact at this stage are listed below. Please follow the links under key contacts for further details of service requirements.
Resources
| Type | Where to find |
|---|---|
| Key contacts | Pharmacy; Imaging; Pathology; ICTU; Research facilities; Tissue Bank; Information governance; New Interventions Committee |
| Useful links | NIHR Clinical Trials Toolkit - NIHR Clinical Trials Toolkit - |
| NIHR benchmark | Prior to NIHR 70-day benchmark |
| Process map links | This activity occurs in the work-up stage: > ³Ô¹ÏºÚÁÏ as sponsor > ³Ô¹ÏºÚÁÏ College Hospital NHS Trust as sponsor > Commercial organisation as sponsor > Non-commercial organisation as sponsor |