Management system guidance

7.0 Support

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7.5 Documented information

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Clause 7.5 sets out what documented information your OH&S management system must contain and how it must be controlled. Documented information means information that has to be controlled and maintained, together with the medium holding it. It can be in any format or media and from any source – procedures, risk assessments, permits, signs, labels, photographs, videos, databases and electronic forms all count. ISO 45001:2018 uses two phrases: to maintain documented information means keeping documents up to date (e.g. procedures, plans, registers), while to retain documented information as evidence means keeping records.

7.5.1 General

Your OH&S management system must include the documented information required by ISO 45001 plus whatever your organization decides is necessary for the system to be effective. The amount will vary depending on the size of the organization and its activities, the need to demonstrate that legal requirements and other requirements are fulfilled, the complexity of processes and the competence of workers. Keep it as simple as possible: a short, well-used safe system of work is better than a long procedure nobody reads. Consult workers on the documented information they need (see 5.4).

Documented information required by ISO 45001:2018

The following checklist shows the documented information the standard explicitly requires, by clause:

  • 4.3 – the scope of the OH&S management system (available as documented information);
  • 5.2 – the OH&S policy (available as documented information);
  • 5.3 – responsibilities and authorities for relevant roles within the OH&S management system (maintained);
  • 6.1.1 – risks and opportunities, and the process(es) and actions needed to determine and address them (6.1.2 to 6.1.4), to the extent needed for confidence that they are carried out as planned (maintained);
  • 6.1.2.2 – the methodology(ies) and criteria for assessing OH&S risks (maintained and retained);
  • 6.1.3 – legal requirements and other requirements, kept up to date when they change (maintained and retained);
  • 6.2.2 – OH&S objectives and the plans to achieve them (maintained and retained);
  • 7.2 – evidence of competence (retained);
  • 7.4.1 – evidence of communications, as appropriate (retained);
  • 7.5.1 – documented information the organization determines is necessary for an effective OH&S management system;
  • 7.5.3 – documented information of external origin needed for planning and operating the system, identified and controlled;
  • 8.1.1 – operational planning and control information, to the extent needed for confidence that processes have been carried out as planned (maintained and retained);
  • 8.2 – the process(es) and plans for responding to potential emergency situations (maintained and retained);
  • 9.1.1 – results of monitoring, measurement, analysis and performance evaluation, and records of maintenance, calibration or verification of measuring equipment (retained);
  • 9.1.2 – results of the evaluation of compliance (retained);
  • 9.2.2 – evidence that the audit programme has been implemented, and the audit results (retained);
  • 9.3 – results of management reviews (retained);
  • 10.2 – the nature of incidents or nonconformities and actions taken, and the results of action and corrective action including their effectiveness (retained; also communicated to relevant workers, workers’ representatives and other relevant interested parties);
  • 10.3 – evidence of continual improvement (maintained and retained).

Many organizations also keep documented information that the standard does not demand but which is useful, such as the results of the context and interested party analyses (4.1 and 4.2), records of worker consultation and participation, hazard identification records, contractor approval records, permits to work, inspection checklists and health surveillance records. Remember that national legislation may require additional records and set minimum retention periods.

7.5.2 Creating and updating

When documented information is created or updated, your organization must ensure that it has appropriate:

  1. identification and description – e.g. title, date, author or reference number;
  2. format and media – e.g. language, software version, graphics, paper or electronic;
  3. review and approval for suitability and adequacy before issue.

Format matters in OH&S: instructions should be in a language and style that the people using them understand, and pictorial work instructions or safety signs may work better than text on the shop floor.

7.5.3 Control of documented information

Documented information required by ISO 45001 and by your OH&S management system must be controlled so that it is available and suitable for use where and when needed, and adequately protected from loss of confidentiality, improper use or loss of integrity. As applicable, your process should address:

  • distribution, access, retrieval and use – e.g. risk assessments and emergency plans accessible at the point of work, read-only versus edit rights;
  • storage and preservation, including keeping records legible – e.g. back-ups, protection from damage in harsh environments;
  • control of changes – e.g. version control, revision history and withdrawal of obsolete copies so out-of-date safe systems of work cannot be used;
  • retention and disposition – e.g. retention periods based on legal requirements (some exposure and health surveillance records must be kept for decades), archiving and secure disposal.

External documents your organization needs, such as legislation, approved codes of practice, manufacturers’ instructions and safety data sheets, must be identified and controlled. ISO 45001 also makes clear that workers, and any workers’ representatives, should be able to access the documented information relevant to them. Treat personal and medical information as confidential and limit access accordingly. Our health and safety management system templates include procedures and forms to help control documents and records.

You should seek and record evidence that your OH&S management system includes all the documented information required by ISO 45001:2018 and that your organization has determined is necessary; that documents are identified, reviewed and approved before issue; that current versions are available at the point of use and obsolete versions are withdrawn; that records are protected, legible, retrievable and kept for defined periods; that external documents are controlled; and that workers and their representatives can access the information relevant to them.

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More information on PDCA

Planning

Context

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
4.1 Organizational Context 4.1 Organizational Context 4.1 Organizational Context
4.2 Relevant Interested Parties 4.2 Relevant Interested Parties 4.2 Workers & Interested Parties
4.3 Management System Scope 4.3 EMS Scope 4.3 OH&S Management System Scope
4.4 QMS Processes 4.4 Environmental Management System 4.4 OH&S Management System

Planning

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
5.1 Leadership & Commitment 5.1 Leadership & Commitment 5.1 Leadership & Commitment
5.2 Quality Policy 5.2 Environmental Policy 5.2 OH&S Policy
5.3 Roles, Responsibilities & Authorities 5.3 Roles, Responsibilities & Authorities 5.3 Roles, Responsibilities & Authorities
    5.4 Consultation & Participation

Support

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
6.1 Risks & Opportunities (6.1.1–6.1.3) 6.1.1 Risks & Opportunities - General 6.1.1 Risks & Opportunities - General
6.2.1 Quality Objectives 6.1.2 Environmental Aspects 6.1.2 Hazard Identification & Assessment
6.2.2 Planning to Achieve Objectives 6.1.3 Compliance Obligations 6.1.3 Legal & Other Requirements
6.3 Planning of Changes 6.1.4 Risks & Opportunities 6.1.4 Planning Action
  6.1.5 Planning Action 6.2.1 OH&S Objectives
  6.2.1 Environmental Objectives 6.2.2 Planning to Achieve Objectives
  6.2.2 Planning to Achieve Objectives  
  6.3 Planning of Changes  
 

Doing

Support

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
7.1 Resources 7.1 Resources 7.1 Resources
7.2 Competence 7.2 Competence 7.2 Competence
7.3 Awareness 7.3 Awareness 7.3 Awareness
7.4 Communication 7.4.1 Communication - General 7.4.1 Communication - General
7.5 Documented Information 7.4.2 Internal Communication 7.4.2 Internal Communication
  7.4.3 External Communication 7.4.3 External Communication
  7.5 Documented Information 7.5 Documented Information

Operations

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
8.1 Operational Planning & Control 8.1 Operational Planning & Control 8.1.1 General
8.2 Customer Requirements 8.2 Emergency Preparedness & Response 8.1.2 Eliminating Hazards
8.3 Design & Development   8.1.3 Management of Change
8.4 Purchasing   8.1.4 Procurement
8.5 Product & Service Provision   8.2 Emergency Preparedness
8.6 Release of Products & Services    
8.7 Nonconforming Outputs    
 

Checking

Monitoring, measurement, analysis and evaluation

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
9.1 Monitoring & Measurement 9.1.1 Performance Evaluation 9.1.1 Performance Evaluation
9.2 Internal Audit 9.1.2 Evaluation of Compliance 9.1.2 Evaluation of Compliance
9.3 Management Review 9.2 Internal Audit 9.2 Internal Audit
  9.3 Management Review 9.3 Management Review
 

Acting

Improvement

ISO 9001:2026
ISO 14001:2026
ISO 45001:2018
10.1 Continual Improvement 10.1 Continual Improvement 10.1 Improvement - General
10.2 Nonconformity & Corrective Action 10.2 Nonconformity & Corrective Action 10.2 Incident, Nonconformity & Corrective Action
    10.3 Continual Improvement
 

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