ClinicalOS guided demo
Preview — in developmentSee ClinicalOS in action
Run a clinical investigation: sites, subjects, monitoring visits, deviations and queries — with a free portal for investigational sites.
Illustrative screens with sample data — no sign-up, nothing to install, and no real customer records. Share this link with anyone.
Step 1 of 5
Study dashboard
Enrolment, data quality and site performance in one place, refreshed from the operational records themselves.
ClinicalOS / Studies / TITAN-PS-001
Prospective post-market study — 12 sites
Subjects enrolled
184 / 240
77% of target
Open queries
23
avg age 4.2 days
Deviations
6
1 major
Monitoring visits
3 due
next in 8 days
What makes ClinicalOS different
The parts a generic document system or spreadsheet cannot do
A free portal for investigational sites
Sponsors invite coordinators into a no-cost, de-identified site workspace — sites never need a licence, which removes the usual barrier to clean data capture.
Datasheets in, structured data out
Upload an existing Excel or CSV datasheet and the importer recognises ODI, VAS, age, visit windows and more, with a field-mapping preview before anything is committed.
Physician-grade instruments
Validated outcome instruments (ODI, VAS, EQ-5D and friends) score themselves, with change-from-baseline computed at each visit.
ISO 14155 safety workflow
Adverse-event and device-deficiency capture follows ISO 14155 with reportability timers and sponsor escalation built in.
HIPAA-aware by construction
PHI access is logged, de-identification is the default for site users, and exports carry the audit trail with them.
Answers, not a sales call
The ten questions everyone asks about ClinicalOS
Answered here in full. Anything else, ask below and you get an immediate answer.
Yes. It is built to ISO 14155 and 21 CFR Part 11 expectations: controlled visits, queries, monitoring, eTMF, safety reporting, audit trail and electronic signature.
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