Nonconformance Control

Nonconformance and CAPA management for GMP and BRCGS manufacturers

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Root Cause to Closure

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Verified CAPA Records

Nonconformance control that prevents recurrence — and satisfies BRCGS and ISO 22716 auditors on evidence and closure

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Structured Nonconformance Logging

Capture deviations, complaints, product failures, and process incidents consistently — with structured fields that ensure no critical information is missed at the point of logging.

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Root Cause Analysis Tools

Identify the underlying causes of nonconformances rather than treating symptoms — using structured root cause tools aligned to ISO 22716 and BRCGS corrective action requirements.

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Corrective and Preventive Actions

Manage corrective and preventive actions through controlled, approved workflows — with defined owners, due dates, and mandatory evidence before any CAPA can be closed.

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Evidence and Verification Control

Actions cannot be closed without supporting evidence and appropriate approval — ensuring every CAPA is genuinely effective, not just administratively complete.

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Trend Identification

Monitor recurring nonconformances across processes, products, and suppliers — identifying systemic weaknesses before they become audit findings or product safety risks.

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Inspection-Ready Records

Full nonconformance histories are structured, retained, and instantly accessible — providing the documented evidence trail that BRCGS and ISO 22716 auditors require.


Why it is important

Because repeated issues indicate system weakness

Cornerstone ensures every nonconformance leads to meaningful, verified corrective action and measurable system improvement — reducing repeat findings and demonstrating a functioning quality system to auditors.

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