Duration: 35-45 minutes to complete
A certificate is issued once a minimum of 80% is achieved in the final quiz section.
Upon completion of this course, you will have an understanding of:
The importance of collecting, recording and reporting adverse events;
The definition for the different categories of adverse events;
The mechanisms used for identifying these events, how they are evaluated when they occur and how follow-up may be carried out;
The necessity of assessing a causal relationship between the study intervention and the adverse event; and
What data is typically reported and who receives the reports.
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