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Category: Management systems

A management system is the documented set of policies, processes and records an organisation uses to run one aspect of its business and prove it is under control. ISO publishes them for quality, information security, environment, occupational health and safety, business continuity, IT service management and more.
Since ISO adopted the Annex SL high-level structure, they share a common skeleton: clauses 4 to 10, covering context, leadership, planning, support, operation, performance evaluation and improvement. Clause 4 has the same shape whether you are reading ISO 9001, ISO 14001 or ISO 45001.
That shared structure is what makes an integrated management system practical. Rather than three sets of policies, three internal audit programmes and three management reviews, you run one system that satisfies several standards at once. Organisations that integrate typically cut audit time and eliminate the contradictions that appear when parallel systems drift apart.
The guides below cover integrated and unified management systems, and the individual standards for environment (ISO 14001), occupational health and safety (ISO 45001), business continuity (ISO 22301), IT service management (ISO 20000) and sector-specific quality standards for medical devices, automotive and food safety.

Business Continuity Plan — guide from Governance Docs

Business Continuity Plan: What ISO 22301 Requires It to Contain

Governance Docs13th August 2026

What a business continuity plan must contain under ISO 22301 clause 8.4: response structure, triggers, warning and communication,…
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Business Impact Analysis — guide from Governance Docs

Business Impact Analysis: How to Do One That Holds Up

Governance Docs13th August 2026

How to run a business impact analysis under ISO 22301 clause 8.2: prioritized activities, MTPD, RTO and RPO,…
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ISO 22301 Mandatory Documents — guide from Governance Docs

ISO 22301 Mandatory Documents and Records, Clause by Clause

Governance Docs13th August 2026

Every document and record ISO 22301:2019 requires by name, clause by clause, plus the ones no clause names…
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ISO 22301 Certification — guide from Governance Docs

ISO 22301 Certification: How the Process Actually Works

Governance Docs13th August 2026

ISO 22301 certification explained: the two audit stages, why the exercise programme decides the outcome, realistic timings, and…
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ISO 45001 Gap Analysis — guide from Governance Docs

ISO 45001 Gap Analysis: What to Check Before You Certify

Governance Docs13th August 2026

How to run an ISO 45001 gap analysis before certification: what to score, how to weight the gaps,…
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ISO 45001 Implementation — guide from Governance Docs

How to Implement ISO 45001: A Ten-Step Plan

Governance Docs13th August 2026

A practical ISO 45001 implementation plan in ten steps, with realistic timings, who needs to be involved, and…
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ISO 45001 Internal Audit Checklist — guide from Governance Docs

ISO 45001 Internal Audit Checklist: Clause 4 to 10

Governance Docs13th August 2026

A clause-by-clause ISO 45001 internal audit checklist, how to build a risk-based audit programme under 9.2, and the…
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ISO 45001 Risk Assessment — guide from Governance Docs

ISO 45001 Risk Assessment: Hazard Identification That Holds Up

Governance Docs13th August 2026

How ISO 45001 risk assessment works under clause 6.1.2: hazard identification, the scoring method you must document, and…
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ISO 45001 Mandatory Documents — guide from Governance Docs

ISO 45001 Mandatory Documents and Records, Clause by Clause

Governance Docs13th August 2026

Every document and record ISO 45001:2018 requires by name, clause by clause, plus the ones that are not…
Read More
ISO 45001 Certification — guide from Governance Docs

ISO 45001 Certification: How the Process Actually Works

Governance Docs13th August 2026

ISO 45001 certification explained end to end: the two audit stages, a realistic timeline, what drives the cost,…
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ISO 13485 Risk Assessment Template — ISO 13485:2016 medical device quality management

ISO 13485 Risk Assessment Template: What It Must Contain

Governance Docs13th August 2026

What an ISO 13485 risk assessment template needs to contain to satisfy clause 7.1 and ISO 14971: the…
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ISO 13485 Internal Audit — ISO 13485:2016 medical device quality management

ISO 13485 Internal Audit: Checklist and Programme Guide

Governance Docs13th August 2026

How to plan and run an ISO 13485 internal audit: a risk-based programme, a clause 4 to 8…
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