About the Oracle InForm to Oracle Argus Safety integration
With this integration, critical data about Serious Adverse Events (SAE) is automatically sent from Oracle InForm to Oracle Argus Safety.
Watch a video overview for this integration.
What does it do?
When a Serious Adverse Event (SAE) occurs during a clinical study, site users and sponsors usually have little time to process the case and report it to regulatory authorities, such as the FDA. In this short span of time, users need to enter AE/SAE data into Oracle InForm, fill out papers or generate a report, send the required documentation to the Safety team, and then Oracle Argus Safety users need to also enter the AE/SAE data in Oracle Argus Safety.
With this integration, AE/SAE data is sent directly from Oracle InForm to Oracle Argus Safety, eliminating the need for transcribing data into Oracle Argus Safety, thus enhancing the transparency of such data to sponsor Safety personnel, and reducing the challenges of reconciling multiple databases.
What products do I need for this integration?
- Oracle Life Sciences Central Designer
- Oracle InForm
- Oracle InForm Publisher
- Oracle Clinical One Digital Gateway
- Standard Services Solution for Argus
- Oracle Argus Safety
For information about the supported versions for each product, see the Oracle Health Sciences Product Compatibility Matrix, which is available for download as an attachment in My Oracle Support article ID 180430.1.
More information
To learn more about setting up this integration, see the Send InForm Safety Data to Argus Safety infographic, which guides you through the full setup process.
Parent topic: Oracle Life Sciences InForm to Oracle Argus Safety