Audit Preparation
Get audit-ready by centralizing policies, procedures, evidence, controls, definitions, corrective actions, and audit history in one place.
Get audit-ready by centralizing policies, procedures, evidence, controls, company definitions, corrective actions, and audit history in one place. Identify gaps against relevant standards, automate evidence collection and reminders, and give teams real-time visibility into what is complete, overdue, or at risk. The result is a faster, more organized path to compliance with less manual tracking and no last-minute surprises.
Capabilities
- Assemble audit evidence packets from ERP, QMS, MES, and supplier systems
- Surface gaps — missing signatures, expired certs, training lapses — before audit
- Map evidence to specific standard clauses (AS9100, ISO 13485, FDA QMSR, FSMA)
- Maintain continuous audit-readiness instead of quarterly reconstruction
Anchor use case
Customer audit evidence packet for parts ABC, lots 1001–1008
A medical device customer requests evidence that operators were trained on the current revision of a work instruction before building lots 1001 through 1008. Structify Industrial returns training records for the five operators, the effective date of the current work instruction revision, production dates, and signoff history — with three gaps surfaced: one operator trained two days after the first lot ran, one acknowledgment missing on second shift, and one supplier cert expired between PO and receipt. Your quality lead reviews the gaps, opens deviations where needed, and ships the packet.
Standards covered
Build timeline
2 to 3 weeks
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