Register subjects in cubeCDMS by signing consent forms. View real-time consent data captured from cubeCDMS. Track subjects' understanding and participation responsibilities through structured consent processes.
Track symptoms and complete daily diaries for the clinical trial. Record patient-reported outcomes and submit responses securely. View study-related information and communicate with study staff through the .
Track study progress, view treatment schedules, and receive reminders for medication and appointments. Access study documents, report adverse events, and communicate with study coordinators. Monitor health metrics and view lab results.
