Subject Management (EDC)

Key Benefits:


  • 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