QMS
Spec-driven quality, from inspection to CAPA.
Overview
QMS-1800 is the quality spine of the platform. Every product carries a versioned specification: acceptance limits, sampling plans, test methods and reference standards. Nothing is inspected against a spec that isn't in force.
Inspections are scheduled from the spec, executed on tablet or terminal, and land immediately on the NC board when they fail. Non-conformances flow through a CAPA lifecycle — containment, root cause, corrective action, verification — with role gates at every step.
Dashboards summarize first-pass yield, NC rate by product and by line, and CAPA effectiveness. Every artifact is exportable as CSV or signed PDF for auditors.
Versioned product specifications, scheduled inspections, non-conformance boards and full CAPA lifecycle — with dashboards, exports and role-based approvals. Designed around HACCP, BRC and ISO 9001 realities.
Capabilities
Every spec is a first-class, versioned artifact bound to the product and its packaging variants. Inspections always reference the active version.
Time-based, batch-triggered and event-triggered inspections, delivered to the right operator at the right station with the right method.
A drag-and-drop non-conformance board flowing into a full CAPA workflow with role separation, e-signatures and verification by qualified auditors.
First-pass yield, defect rate, NC cycle time, CAPA effectiveness — all sliced by product, line, shift and customer.
Signed PDF certificates of conformance, CSV extracts, and API endpoints for BI tools and customer portals.
Operator, inspector, quality engineer, auditor and admin — five roles, strict separation of duties, full audit log.
Modules included
Specifications
Where it fits
- Food manufacturers under HACCP, BRC or IFS certification
- Pharmaceutical and medical-device makers requiring 21 CFR Part 11
- Contract manufacturers needing per-customer quality certificates
- Multi-plant quality organizations with shared spec libraries