Manage patient enrollment, visit schedules, data collection, adverse event reporting, and regulatory submissions for clinical trials.
Interactive diagram showing apps, databases, and data flow. Hover over components to see connections. Click databases to view table schemas.
Participant Enrollment
Screen, consent, and enrol participants with eligibility verification and e-consent capture.
Visit Scheduler
Plan and track all study visits with automated reminders for participants and coordinators.
Data Collection Forms
Structured eCRF entry per visit with validation rules and query management.
Safety & Adverse Events
Log, grade, and escalate adverse events with automatic routing to the medical monitor.
Regulatory Dashboard
Track IRB submissions, protocol amendments, and compliance milestones.
Participants & Consent
Participant demographics, eligibility records, consent versions, and enrollment status.
Visits & eCRF Data
Visit schedules, completed forms, data queries, and investigator sign-offs.
Safety & Regulatory
Adverse event reports, protocol deviations, IRB submissions, and audit logs.
Configure the study protocol including visit schedule, eligibility criteria, and eCRF templates.
Add investigator sites, assign coordinators, and configure site-specific settings.
Upload IRB-approved consent documents and configure the e-consent workflow.
Walk coordinators and investigators through data entry, query resolution, and AE reporting.
Run a test enrollment end-to-end to verify all workflows before first patient first visit.
