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 This article was published on 2024-11-07
