Clinical Trial Lite Manager
Protocol tracking, enrollment logs, and essential-document checklists sized for a 1-3 study site.
The problem it solves
A small investigator-initiated trial doesn't need a full CTMS, but it still needs real enrollment tracking, adverse-event logging against a real reporting clock, and essential-document checklists — and those usually end up split across email, a shared drive, and someone's memory.
How it works
- 1Track the study and its essential-document checklist in one place.
- 2Log enrollment by coded participant ID only — no name or date of birth is captured.
- 3Log adverse events against a 15-day reporting-clock computation, with a sponsor-report attestation step.
Who it’s for
Investigator-initiated trial coordinators running 1-3 active study sites.
Is this sized for a large multi-site trial?
No — it's deliberately scoped for a small, investigator-initiated trial with a handful of sites, not a full sponsor-run CTMS workload.