Audit Readiness Intelligence
Continuous audit readiness, not last-minute scrambles.
An FDA inspection is announced. The compliance team has 48 hours to assemble evidence across quality systems, deviation records, CAPA logs, and training documentation.
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-70% Audit Prep Time
-45% Finding Reduction
The Problem
Audit readiness in regulated industries is typically a reactive, high-stress exercise. Evidence is scattered. Documentation gaps are discovered late. Compliance teams scramble to assemble what should have been continuously maintained.
The Transformation
OpsIQ Audit Readiness Intelligence maintains a continuous state of audit readiness by automatically assembling evidence lineage, generating trust receipts, and surfacing compliance gaps before auditors arrive.