About the Oracle InForm to Oracle Argus Safety integration
Oracle 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 Oracle InForm to Oracle Argus Safety integration automates the reporting of these events, enabling sponsors to reliably acquire relevant information for their studies.
Using the Oracle Central Designer data mapping feature, you define the data that is sent to Oracle Argus Safety as well as which changes trigger a follow up.
The Oracle InForm Publisher component monitors your Oracle InForm study database and sends adverse event information and other information such as medical history, concomitant medications, and labs to Oracle Argus Safety based on either the time frames you configure in Oracle InForm Publisher or the data entered into Oracle InForm.
For more information, see: