ISO 9001 focus

Structured around how ISO 9001 audits are conducted for manufacturing environments.

Audit readiness, plain English

The system organises evidence so auditors can trace requirements quickly: documented information with approvals, risks and objectives linked to actions, NCRs and CAPAs with effectiveness checks, and management reviews with decisions and follow-up.

Evidence stays controlled, with exportable packs aligned to manufacturing audit flows.

How it maps

Context and scope
Documented information
Risks and objectives
Internal audits
Nonconformities and corrective actions
Management review
Supplier control and incoming inspection

ISO certification depends on your implementation and audit results; the software supports organisation and control of evidence.