Clinical Engagement | Life Sciences Cloud Developer Guide

Adverse Events
Adverse Events data model helps you in managing and documenting any unfavorable or unintended signs, symptoms, or diseases that occur in participants during the research study. These adverse events can include a wide range of physical or psychological effects that varies from mild discomfort to serious health complications.

Participant Management
Participant Management data model helps you to streamline the recruitment and enrollment processes in clinical trials with advanced digital solutions. With this data model, you can store clinical trial data representing care programs and research studies. It’s USCDI and FHIR R4-aligned, which helps with your system's interoperability and compliance while managing participant data efficiently.

Site Management
The Site Management data model helps life sciences organizations identify suitable sites for conducting research studies. Study managers can search for the sites and investigators using the Criteria-Based Search and Filter, and send them assessments. From the assessment responses, study managers can assign scores to the sites, investigators, and their responses. They can also tag the sites and investigators for future site selection efforts.