EvidenceOS guided demo
Preview — in developmentSee EvidenceOS in action
Build clinical evidence for orthopedic and spinal implants: registries, literature, appraisal and a defensible evaluation report.
Illustrative screens with sample data — no sign-up, nothing to install, and no real customer records. Share this link with anyone.
Step 1 of 4
Evidence dashboard
Every evidence source for a device family in one register — registries, literature, internal studies, post-market data.
EvidenceOS / Dashboard
Evidence position — TITAN-PS
Included studies
42
of 318 screened
Registry datasets
3
auto-synced
Appraised
38
4 pending
CER status
Draft v2
review due 2026-04-01
What makes EvidenceOS different
The parts a generic document system or spreadsheet cannot do
Registries you can stand up in a day
Implant, procedure and participant models are ready-made for orthopedic and spinal implants — no bespoke database build before first enrolment.
Auto-created from ClinicalTrials.gov
Paste an NCT ID and the study, sites and arms are pulled from the ClinicalTrials.gov v2 API and turned into a working registry.
Evidence that flows into regulatory work
Registry outputs feed clinical evaluation and PMCF sections directly, so post-market evidence and MDR reporting share one source.
Signed, inspection-ready exports
Every export is a dated package with signature manifest and audit trail rather than a loose spreadsheet.
Answers, not a sales call
The ten questions everyone asks about EvidenceOS
Answered here in full. Anything else, ask below and you get an immediate answer.
Real-world evidence: implant registries, participants, procedures, visits and safety events, plus literature appraisal feeding clinical evaluation.
Ready to use EvidenceOS with your own records?
Start a subscription, or ask us for a live walkthrough with your device portfolio.