1. UK-wide study (lead R&D office in other UK nation)
Applicant submits R&D application to other UK nation eg. to NIHR CSP Unit via IRAS
CSP Unit forwards IRAS R&D Form promptly to Permissions CC, along with global documents available at that time
Lead CLRN collates global documents and carries out global governance checks
Permissions CC contacts study contact promptly to recommend submitting to Scotland (via Permissions CC) in parallel, as well as remind about Scottish SSI Forms for local Scottish PI(s)
If ‘No’
If ‘Yes’
Permissions CC waits for global documents and Governance Report from Lead CLRN
Follow process as if lead R&D office is in Scotland
[no documents/CofC need be forwarded
to other UK nation(s)]
Mini-generic Review for Scotland
Local Review(s) Scottish sites
Certificate of Compliance
For each Scottish Health Board: Local management permission letter