CAPA Report in QMS: The Complete 2026 Guide to Corrective and Preventive Action
16 min read
A CAPA report stands as the operational proof that your quality management system actually works. Within FDA-regulated facilities, medical device manufacturers, and pharmaceutical operations, the CAPA process determines whether discovered problems get fixed comprehensively or simply masked temporarily. Regulators, auditors, and customers no longer accept surface-level compliance. They expect evidence-based systems that identify root causes, […]
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