CR001 Establishing and Maintaining Investigator Site Files, Trial Master Files and Sponsor Files SOP Delegation of TMF form Document Checklist CTIMP Document Checklist non-CTIMP Document Checklist Medical Device
CR003 Suspected Serious Breaches CR003 Suspected Serious Breaches v5.0.pdf Suspected Serious Breach Report
CR004 Recording and Reporting Study Data SOP Source Data Plan Example Text for Medical Notes AWI Consent
CR005 Identifying, Recording and Reporting Adverse Events and Urgent Safety Measures for CTIMPs Identifying Recording and Reporting AEs and USMs for CTIMPs Cover Sheet and Return Receipt Pregnancy Notification Form CTIMP SAE Form AE Flowchart - Reporting AE Flowchart - Identifying Parent Child SAE form (CTIMP) CTIMP AE Log CTIMP SAE Follow Up Sign-Off
CR006 Identifying, Recording and Reporting Adverse Events and Urgent Safety Measures for Non-CTIMPs Identifying Recording and Reporting AEs and USMs for Clinical Trials not Involving IMPs Cover Sheet and Return Receipt Non-CTIMP SAE Form Adverse Event Flowchart - Reporting non-CTIMP AE log SAE non-CTIMP Follow-Up Sign-Off
CR007 Study Documents SOP CTIMP Protocol Template Non-CTIMP Protocol Template PIS & CF Template PIS & CF AWI Template PIS & CF Recovered Capacity Template GP Letter Template Site Signature & Delegation Log Subject Pre-screening Log Consent Subject Status Log Study Specific Training Record Data Only Protocol Template Qualitative Protocol Template
CR010 Management of Protocol and GCP Deviations and Violations SOP Protocol / GCP Violation Reporting Form Protocol / GCP Deviation Log
