QualityOS guided demo
See QualityOS in action
Walk the quality system end to end: a controlled document, a CAPA, a change order that creates training, and the trending view an inspector asks for.
Illustrative screens with sample data — no sign-up, nothing to install, and no real customer records. Share this link with anyone.
Step 1 of 6
The quality dashboard
Everything overdue, everything approaching a clock, in one view. Counters are live records — not a report someone assembled last Friday.
QualityOS / Dashboard
Quality system health
Open CAPAs
7
2 approaching due date
Documents in review
12
avg 4.1 days
Training compliance
96%
3 assignments overdue
Complaints open
4
1 reportability decision due
| Record | Owner | Due | Status |
|---|---|---|---|
| CAPA 26-014 — Sterile barrier defect | M. Okafor | in 3 days | On track |
| CMP 26-031 — Screw driver fracture | L. Nguyen | tomorrow | Escalated |
| NC 26-008 — Out of spec anodizing | R. Patel | overdue 2 days | Overdue |
What makes QualityOS different
The parts a generic document system or spreadsheet cannot do
Records that carry their own clocks
Complaints, CAPAs and nonconformances are numbered CMP/CAPA/NC 26-XXX with an automatic annual reset, and each one runs a due-date clock with escalation instead of a reminder someone has to remember to send.
Change orders that create the training
Approving a document change order generates the training assignments for every affected role, so effectivity and competence stay in step without a second system.
One click to an inspection pack
Document history, approvals, CAPA evidence and training matrices export as a single dated, signed inspection-readiness pack — the same artefact an FDA or notified-body auditor asks for.
Multi-framework by design
The same record satisfies FDA QSR/QMSR, EU MDR, UK MDR and Health Canada CMDR scope; you pick the frameworks per company and the checklists follow.
Validated, not 'validatable'
A completed URS/IQ/OQ/PQ software-validation package with version history ships with the product, so your CSV effort is a review rather than a project.
Answers, not a sales call
The ten questions everyone asks about QualityOS
Answered here in full. Anything else, ask below and you get an immediate answer.
Document control, CAPA, complaints, nonconformance, change orders, training, internal and supplier audits, equipment, risk management (ISO 14971), management review, post-market surveillance and lot release — all as linked records rather than separate trackers.
Ready to use QualityOS with your own records?
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