Document and Export Adverse Events
TrialPath | Enterprise
Adverse events are unfavorable, unintended signs, symptoms, or diseases that may or may not result from the clinical trial. In TrialPath, you can document adverse event details in a participant record. If applicable, you can also enter a protocol defined event to trigger associated charges in Finance. In TrialPath, you can view and export adverse events for a participant or study. To view and export adverse events at the network level, use Enterprise.
Click the options below to open guides and video tutorials.
