10 likes | 122 Views
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.
E N D
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