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Tag: serious adverse events

28Dec

Serious vs Non-Serious Adverse Events: When to Report in Clinical Trials

Posted by Kimberly Vickers — 13 Comments
Serious vs Non-Serious Adverse Events: When to Report in Clinical Trials

Learn how to correctly classify and report serious vs non-serious adverse events in clinical trials. Understand the 6 FDA criteria for seriousness, avoid common mistakes, and meet reporting deadlines to keep trials compliant and patients safe.

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