Key Benefits:
Sponsor/CRO
- Integrated electronic data capture and retention system
- Integrated adverse event entry with endpoint adjudication
- Increase retention through IRB approved SMS messaging
Clinical Site
- Central document management capabilities for capturing source documentation
- Floating data entry hints within all Case Report Forms
- Manage all enrolled subjects within a central visit scheduler
Key Features:
Visit Scheduling & CRF Completion
- Complete visits and CRF data entry within an intuitive interface
Configurable Entity Workflow
- Customize subject, visit, adverse event and form workflows to comply with the study protocol and industry best practices
Adverse Events
- Capture events with built-in support for SAE reporting to the FDA