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ISO 13485 Documentation Explained: From QMS Basics to Audit Readiness

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This practical blog explains what ISO 13485 documentation includes, why it matters for certification, and how proper document control ensures consistent processes, audit readiness, and regulatory compliance across the medical device lifecycle. https://13485certificationprocedures.wordpress.com/2025/12/22/iso-13485-documentation-basics-a-practical-introduction-for-medical-device-organizations/

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