Quality software for regulated manufacturing

Evidence you can hand to an auditor.

Three systems for aerospace and regulated manufacturers: investigate the cause, prove the measurement, control the record. Every consequential decision carries a named human, a date, and evidence that survives a review.

Built around AS9100 · AS9102 · ISO 17025 · Nadcap workflows

OK to useCAL 2027-01-15
One spine, three systems

A finding is only closed when all three are true.

Most quality software owns one of these and gestures at the others. Each of ours owns its part completely and hands off a record the next one can stand on.

  1. 01

    Investigate the cause

    CauseProof

    Guided analysis that challenges weak causality and refuses to close a problem on a cause nobody verified.

  2. 02

    Prove the measurement

    GageProof

    Scan a gage before you measure. When one comes back out of tolerance, the record already knows which jobs it touched.

  3. 03

    Control the record

    QMSProof

    Document control, CAPA and audit readiness in one authoritative place, so every corrective action has a permanent home.

The portfolio

Three products. One standard of proof.

CauseProof

Solve the right problem. Prove the cause.

Root-cause investigation for quality teams. Guided analysis that challenges weak causality and links every corrective action to a cause that was actually verified — approvals, customer SCAR commitments and effectiveness checks on one dated, auditable record.

  • Human approval mandatory
  • Dated audit trail
  • SCAR commitments
Open CauseProof →

GageProof

Know the gage was good.

Calibration and gage control at the point of use. Scan before you measure and get OK TO USE or DO NOT USE. When an instrument comes back out of tolerance, the record already knows every job it touched since its last good calibration.

  • QR scan at point of use
  • Out-of-tolerance recall
  • Certificate review
Open GageProof →

QMSProof

Audit-ready. Always.

The controlled quality management system. Owns the CAPA record end to end — document control, compliance tracking and continuous audit readiness — so every corrective action has one authoritative home.

  • Document control
  • CAPA of record
  • Continuous audit readiness
Open QMSProof →
What an auditor sees

A record, not a report.

Every controlled decision is written server-side with the person who made it, the moment they made it, and the evidence it rested on. Nothing consequential can be edited from a browser.

  • AS9100
  • AS9102 / FAIR
  • ISO 17025
  • Nadcap
  • ISO 9001
  • 8D / CAPA
Controlled recordimmutable
Problem
PRB-2041 · Bushing bore oversize
Verified cause
Reamer wear beyond control limit
Corrective action
CA-118 · Tool-life ceiling reduced
Approved by
M. Carter · Quality Manager
Effectiveness
30-day check · 0 recurrence
Gage at time of use
INST-100 · in tolerance
Next step

Twenty minutes, your process, no slides.

Bring a real finding — a customer SCAR, a failed audit item, an out-of-tolerance gage. We will walk it through the system and you will see exactly what the record looks like at the end.