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Category: Articles

ISO 13485 Certification — ISO 13485:2016 medical device quality management

ISO 13485 Certification Explained: A Clear, Essential Guide

Governance Docs13th August 2026

ISO 13485 certification explained: the audit stages, realistic timeline and cost drivers, what a notified body actually checks,…
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ISO clause 10 improvement explained — Annex SL harmonized structure

ISO Clause 10: Improvement Explained

Governance Docs13th August 2026

What clause 10 of the ISO harmonized structure requires, why the sub-clause numbers differ between standards, and correction…
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ISO clause 9 performance evaluation explained — Annex SL harmonized structure

ISO Clause 9: Performance Evaluation Explained

Governance Docs13th August 2026

What clause 9 of the ISO harmonized structure requires: monitoring and measurement, risk-based internal audit, and management review…
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ISO clause 8 operation explained — Annex SL harmonized structure

ISO Clause 8: Operation Explained

Governance Docs13th August 2026

What clause 8 of the ISO harmonized structure requires, and how far it expands in ISO 9001, ISO…
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ISO clause 7 support explained — Annex SL harmonized structure

ISO Clause 7: Support Explained

Governance Docs13th August 2026

What clause 7 of the ISO harmonized structure requires: resources, competence, awareness, communication and documented information.
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ISO clause 6 planning explained — Annex SL harmonized structure

ISO Clause 6: Planning Explained

Governance Docs13th August 2026

What clause 6 of the ISO harmonized structure requires: risks and opportunities, measurable objectives, and the 2021 addition…
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ISO clause 5 leadership explained — Annex SL harmonized structure

ISO Clause 5: Leadership Explained

Governance Docs13th August 2026

What clause 5 of the ISO harmonized structure requires: leadership and commitment, policy, and roles, responsibilities and authorities.
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ISO clause 4 context of the organization explained — Annex SL harmonized structure

ISO Clause 4: Context of the Organization Explained

Governance Docs13th August 2026

What clause 4 of the ISO harmonized structure requires: context, interested parties, scope and processes, including the 2024…
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ISO 14971 explained — medical device risk management

ISO 14971: The Risk Management File and Where Files Break

Governance Docs13th August 2026

What ISO 14971:2019 requires, the four places risk management files reliably break, and one widely repeated error about…
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Point-of-care testing governance under ISO 15189

Point-of-Care Testing Governance After ISO 22870

Governance Docs13th August 2026

ISO 22870 is withdrawn and point-of-care testing now sits inside ISO 15189. Deployment, operator authorisation at ward scale,…
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Critical value reporting in a medical laboratory

Critical Value Reporting: Getting the Result to Someone Who Can Act

Governance Docs13th August 2026

Building a critical value list that works, the read-back, escalation when nobody answers, and the one measure that…
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Pre-analytical errors — where laboratory mistakes actually happen

Pre-analytical Errors: Where Laboratory Mistakes Actually Happen

Governance Docs13th August 2026

What goes wrong before the examination starts, why the laboratory's controls are weakest exactly where the risk is…
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