Templates to help you prepare study documents that meet current regulatory and research governance standards. Protocols CR007-T01 CTIMP Protocol Template v11.0CR007-T02 Non CTIMP Protocol Template v7.0 CR007-T19 Data Only Protocol Template v3.0CR007-T20 Qualitative Protocol Template v3.0CR007-T21 Qualitative UoE Protocol Template v2.0CR007-T23 Medical Device Protocol Template v2.0 PIS and consent CR007-T03 PIS and Consent Form Template v10.0 CR007-T03 PIS and Consent Form Template Two Column Layout v10.0 CR007-T04 PIS and Consent Form AWI Template v10.0CR007-T05 PIS and Consent Form Recovered Capacity Template v10.0 CR007-T22 Qualitative UoE PIS and Consent Form Template v3.0CR007-T06 GP Letter Template v3.0 Pharmacovigilance CR008-T01 DSUR Template v3.0CR005-T01 CTIMP SAE Form v9.0CR005-T05 CTIMP AE Log v5.0 CR005-F02 Pregnancy Notification Form v10.0 CR006-T01 Non CTIMP SAE Form v7.0 CR006-T03 Non CTIMP AE Log v2.0CR012-T01 SAE CIMD Form v4.0 CR012-T02 Medical Device Deficiency Form v4.0 Global health GH001-T01 Global Health Non-CTIMP Protocol Template v2.0 GH001-T02 Global Health Data Only Protocol Template v2.0 GH001-T03 Global Health Qualitative Protocol Template v2.0 GH001-T04 Global Health PIS v2.0 Monitoring CR007-T12 Staff Signature and Delegation Log of Responsibilities v4.0 CR007-T13 Pre-Screening Log v3.0CR007-T14 Consent & Participant Status Log v3.0 CR007-T17 Study Specific Training Record v3.0 This article was published on 2025-03-17
