Introduction to Collecting and Reporting Adverse Events
- This short course provides a general introduction and overview of Adverse Events and how to deal with them when they occur. This course is suitable for everyone involved in clinical research.
Data Safety Monitoring Boards for Clinical Trials
- This course outlines the role of a Data Safety and Monitoring Board (DSMB) during a clinical trial. Appointed by the trial's sponsors, the DSMBs are responsible for assessing the overall progress of the trial and focusing in particular on analysing the safety and efficacy data.