Study setup & management
Register protocols with phase, indication, sponsor and enrollment targets, then track them from startup to close-out.
Platform capabilities
Register protocols with phase, indication, sponsor and enrollment targets, then track them from startup to close-out.
Investigator of record, geography, activation milestones and enrollment capacity across the whole site network.
De-identified screening and subject registry with randomization arm, screen failures and withdrawals.
Protocol visit schedules with window tolerance, completion capture and out-of-window escalation.
Initiation, interim and close-out visits with source data verification findings and query resolution burden.
Adverse event severity, seriousness and causality assessment beside categorized protocol deviations.
IRB and ethics approvals, 1572s, contracts and IND submissions with expiry and pending-status alerts.
Every create, update and delete captured automatically with actor and timestamp for inspection readiness.
Portfolio-level enrollment against target, safety signal counts, query burden and regulatory exposure in a single dashboard.
Visit-by-visit findings, source data verification outcomes and open queries by site, with escalation for out-of-window visits.
Fast participant registration and visit capture for site staff; complete, filterable change history for quality and inspection teams.
Sign in with your organization account to reach the operational workspace.
Sign in to MedValue Clinical Trials Pro