About the InForm to Argus Safety integration

Argus Safety is a pharmacovigilance platform that allows sponsors to procure clinically significant adverse event (AE) or serious adverse event (SAE) information on drug subjects. The InForm to Argus Safety integration automates the reporting of these events, enabling sponsors to reliably acquire relevant information for their studies.

Using the Central Designer data mapping feature, you define the data that is sent to Argus Safety as well as which changes trigger a follow up.

The InForm Publisher component monitors your InForm study database and sends adverse event information and other information such as medical history, concomitant medications, and labs to Argus Safety based on either the time frames you configure in InForm Publisher or the data entered into InForm.