Management system guidance

4.0 Context of the Organization

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4.3 Determining the scope of the environmental management system

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Defining the scope of your environmental management system is a key early step. The scope sets out the physical and organizational boundaries the EMS applies to: which sites, which activities, products and services, and which parts of the organization. Your organization has freedom to choose its boundaries. It can apply the EMS across the whole organization or only to specific parts of it, provided top management for those parts has the authority to establish an EMS.

When setting the scope, your organization must consider the external and internal issues from 4.1, the compliance obligations from 4.2, its organizational units, functions and physical boundaries, its activities, products and services, and how far it has the authority and ability to control and influence them across their life cycle. Once the scope is set, everything the organization does within those boundaries must be covered by the EMS.

What changed in ISO 14001:2026

Item e) now expressly links control and influence to the life cycle of your activities, products and services, so the scope decision should reflect a life cycle perspective (see 3.3.3 Life cycle). The scope must now be ‘available as documented information’ rather than ‘maintained’, and it must still be available to interested parties. Annex A clarifies that this availability requirement applies once your organization claims conformity with the standard.

Considering boundaries and applicability

From a review of your operations, products and services, the natural boundaries of the EMS are usually apparent from the processes and controls already in place. Points to consider include:

  • The sites, buildings, land and remote or temporary locations involved;
  • The range of activities, products and services provided;
  • Externally provided processes, products and services, such as contract manufacturing, transport or waste management;
  • Support provided by centralized functions or a parent company, such as purchasing, HR or design;
  • Where your products are used and how they are treated at end of life.

If your organization relies on a corporate or regional office for key functions such as resource allocation or decision-making, think about how that relationship affects what you can realistically control within the scope.

Control and influence across the life cycle

You must decide how much control or influence you have over each stage of the life cycle, from raw materials and purchased goods through your own operations to distribution, use and disposal. You will usually have full control over activities on your own site, partial control over contractors working there, and only influence over suppliers, customers and end users. A life cycle perspective does not require a formal life cycle assessment; careful thought about each stage is sufficient. Record your conclusions, as they also feed into the determination of environmental aspects in 6.1.2 and the controls over externally provided processes in 8.1.

Credibility of the scope

The credibility of the EMS depends on the boundaries chosen. The scope should be a factual and representative statement of the operations included and must not be used to leave out activities, products, services or facilities with significant environmental aspects, or to avoid compliance obligations. Certification auditors will challenge a scope that appears to exclude a site with a waste treatment plant, a high-impact process or an area with environmental permits. Unlike ISO 9001, ISO 14001 has no concept of excluding requirements that are not applicable; all requirements apply to everything within the scope.

Documenting the scope

The scope must be available as documented information, usually in your environmental manual or a scope statement, and it must be available to interested parties who ask for it, for example on your website or on request. A good scope statement names the sites covered and summarizes the activities, products and services. The certificate wording is normally shorter. For example:

‘The design, manufacture and distribution of corrugated packaging products at the Northfield site, including associated warehousing and transport activities.’

‘The provision of commercial cleaning and facilities management services from the head office and regional depots, including services delivered at client premises.’

Review the scope when there are significant changes, such as new sites, acquisitions, new product lines or changes in compliance obligations, and plan the change as described in 6.3. Agree the certification scope with your certification body early in the process. If you need a template to help document your scope, see our environmental manual template.

You should seek and record evidence that your organization has determined the boundaries and applicability of the EMS after considering its context, compliance obligations, organizational units, functions, physical boundaries, activities, products and services, and its control and influence over their life cycle; that no activities with significant environmental aspects have been inappropriately excluded; and that the scope is available as documented information and to interested parties.

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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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