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ISO 37301:2021(en)
ISO - Cover page
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Context of the organization
 4.1 Understanding the organization and its context
 4.2 Understanding the needs and expectations of interested parties
 4.3 Determining the scope of the compliance management system
 4.4 Compliance management system
 4.5 Compliance obligations
 4.6 Compliance risk assessment
5 Leadership
 5.1 Leadership and commitment
  5.1.1 Governing body and top management
  5.1.2 Compliance culture
  5.1.3 Compliance governance
 5.2 Compliance policy
 5.3 Roles, responsibilities and authorities
  5.3.1 Governing body and top management
  5.3.2 Compliance function
  5.3.3 Management
  5.3.4 Personnel
6 Planning
 6.1 Actions to address risks and opportunities
 6.2 Compliance objectives and planning to achieve them
 6.3 Planning of changes
7 Support
 7.1 Resources
 7.2 Competence
  7.2.1 General
  7.2.2 Employment process
  7.2.3 Training
 7.3 Awareness
 7.4 Communication
 7.5 Documented information
  7.5.1 General
  7.5.2 Creating and updating documented information
  7.5.3 Control of documented information
8 Operation
 8.1 Operational planning and control
 8.2 Establishing controls and procedures
 8.3 Raising concerns
 8.4 Investigation processes
9 Performance evaluation
 9.1 Monitoring, measurement, analysis and evaluation
  9.1.1 General
  9.1.2 Sources of feedback on compliance performance
  9.1.3 Development of indicators
  9.1.4 Compliance reporting
  9.1.5 Record-keeping
 9.2 Internal audit
  9.2.1 General
  9.2.2 Internal audit programme
 9.3 Management review
  9.3.1 General
  9.3.2 Management review inputs
  9.3.3 Management review results
10 Improvement
 10.1 Continual improvement
 10.2 Nonconformity and corrective action
Annex A (informative) Guidance for the use of this document
Bibliography
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International

Standard

ISO 37301
Compliance management systems — Requirements with guidance for use
Systèmes de management de la conformité — Exigences et recommandations pour la mise en oeuvre
Reference number
ISO 37301:2021(en)
First edition
2021-04
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ContentsPage

Foreword

ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the different types of ISO documents should be noted. This document was drafted in accordance with the editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of any patent rights identified during the development of the document will be in the Introduction and/or on the ISO list of patent declarations received (see www.iso.org/patents).
Any trade name used in this document is information given for the convenience of users and does not constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and expressions related to conformity assessment, as well as information about ISO's adherence to the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/iso/foreword.html.
This document was prepared by Technical Committee ISO/TC 309, Governance of organizations.
This first edition of ISO 37301 cancels and replaces ISO 19600:2014, which has been technically revised.
The main changes compared to ISO 19600:2014 are as follows:
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this document now contains requirements with additional guidance for use based on those requirements;
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this document follows ISO’s requirements for a harmonized structure for management system standards.
Any feedback or questions on this document should be directed to the user’s national standards body. A complete listing of these bodies can be found at www.iso.org/members.html.

Introduction

Organizations that aim to be successful in the long term need to establish and maintain a culture of compliance, considering the needs and expectations of interested parties. Compliance is therefore not only the basis, but also an opportunity, for a successful and sustainable organization.
Compliance is an ongoing process and the outcome of an organization meeting its obligations. Compliance is made sustainable by embedding it in the culture of the organization and in the behaviour and attitude of people working for it. While maintaining its independence, it is preferable that compliance management is integrated with the organization’s other management processes and its operational requirements and procedures.
An effective, organization-wide compliance management system enables an organization to demonstrate its commitment to comply with relevant laws, regulatory requirements, industry codes and organizational standards, as well as standards of good governance, generally accepted best practices, ethics and community expectations.
An organization’s approach to compliance is shaped by the leadership applying core values and generally accepted good governance, ethical and community standards. Embedding compliance in the behaviour of the people working for an organization depends above all on leadership at all levels and clear values of an organization, as well as an acknowledgement and implementation of measures to promote compliant behaviour. If this is not the case at all levels of an organization, there is a risk of noncompliance.
In a number of jurisdictions, courts have considered an organization’s commitment to compliance through its compliance management system when determining the appropriate penalty to be imposed for contraventions of relevant laws. Therefore, regulatory and judicial bodies can also benefit from this document as a benchmark.
Organizations are increasingly convinced that, by applying binding values and appropriate compliance management, they can safeguard their integrity and avoid or minimize noncompliance with the organization’s compliance obligations. Integrity and effective compliance are therefore key elements of good and diligent management. Compliance also contributes to the socially responsible behaviour of organizations.
One of the objectives of this document is to assist organizations to develop and spread a positive culture of compliance, considering that an effective and sound management of compliance-related risks should be regarded as an opportunity to pursue and take, due to the several benefits that it provides to the organization such as:
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improving business opportunities and sustainability;
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protecting and enhancing an organization’s reputation and credibility;
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taking into account expectations of interested parties;
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demonstrating an organization’s commitment to managing its compliance risks effectively and efficiently;
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increasing the confidence of third parties in the organization’s capacity to achieve sustained success;
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minimizing the risk of a contravention occurring with the attendant costs and reputational damage.
This document specifies requirements as well as provides guidance on compliance management systems and recommended practices. Both the requirements and the guidance in this document are intended to be adaptable, and implementation can differ depending on the size and level of maturity of an organization’s compliance management system and on the context, nature and complexity of the organization’s activities and objectives.
This document is suitable to enhance the compliance-related requirements in other management systems and to assist an organization in improving the overall management of all its compliance obligations.
Figure 1 provides an overview on common elements of a compliance management system.
Figure 1 — Elements of a compliance management system
graphic
In this document, the following verbal forms are used:
—
“shall” indicates a requirement;
—
“should” indicates a recommendation;
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“may” indicates permission;
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“can” indicates a possibility or a capability.
Information marked as “NOTE” is for guidance in understanding or clarifying the associated requirements.
Annex A provides guidance for the use of this document.
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International StandardISO 37301:2021(en)
Compliance management systems — Requirements with guidance for use

1Scope

This document specifies requirements and provides guidelines for establishing, developing, implementing, evaluating, maintaining and improving an effective compliance management system within an organization.
This document is applicable to all types of organizations regardless of the type, size and nature of the activity, as well as whether the organization is from the public, private or non-profit sector.
All requirements specified in this document that refer to a governing body apply to top management in cases where an organization does not have a governing body as a separate function.

2Normative references

There are no normative references in this document.

3Terms and definitions

For the purposes of this document, the following terms and definitions apply.
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
—
ISO Online browsing platform: available at https://www.iso.org/obp
—
IEC Electropedia: available at http://www.electropedia.org/
3.1
organization
person or group of people that has its own functions with responsibilities, authorities and relationships to achieve its objectives (3.6)
Note 1 to entry: The concept of organization includes, but is not limited to, sole-trader, company, corporation, firm, enterprise, authority, partnership, charity or institution, or part or combination thereof, whether incorporated or not, public or private.
Note 2 to entry: If the organization is part of a larger entity, the term “organization” refers only to the part of the larger entity that is within the scope of the compliance management system.
3.2
interested party (preferred term)
stakeholder (admitted term)
person or organization (3.1) that can affect, be affected by, or perceive itself to be affected by a decision or activity
3.3
top management
person or group of people who directs and controls an organization (3.1) at the highest level
Note 1 to entry: Top management has the power to delegate authority and provide resources within the organization.
Note 2 to entry: If the scope of the management system (3.4) covers only part of an organization, then top management refers to those who direct and control that part of the organization.
Note 3 to entry: For the purposes of this document, the term “top management” refers to the highest level of executive management.
3.4
management system
set of interrelated or interacting elements of an organization (3.1) to establish policies (3.5) and objectives (3.6) as well as processes (3.8) to achieve those objectives
Note 1 to entry: A management system can address a single discipline or several disciplines.
Note 2 to entry: The management system elements include the organization’s structure, roles and responsibilities, planning and operation.
3.5
policy
intentions and direction of an organization (3.1), as formally expressed by its top management (3.3)
Note 1 to entry: A policy can also be formally expressed by an organization’s governing body (3.21).
3.6
objective
result to be achieved
Note 1 to entry: An objective can be strategic, tactical, or operational.
Note 2 to entry: Objectives can relate to different disciplines (such as finance, health and safety, and environment). They can be, for example, organization-wide, or specific to a project, product, service or process (3.8)).
Note 3 to entry: An objective can be expressed in other ways, e.g. as an intended result, a purpose, an operational criterion, as a compliance (3.26) objective, or by the use of other words with similar meaning (e.g. aim, goal, or target).
Note 4 to entry: In the context of compliance management systems (3.4), compliance objectives are set by the organization (3.1), consistent with the compliance policy (3.5), to achieve specific results.
3.7
risk
effect of uncertainty on objectives (3.6)
Note 1 to entry: An effect is a deviation from the expected – positive or negative.
Note 2 to entry: Uncertainty is the state, even partial, of deficiency of information related to, understanding or knowledge of, an event, its consequence, or likelihood.
Note 3 to entry: Risk is often characterized by reference to potential “events” (as defined in ISO Guide 73) and “consequences” (as defined in ISO Guide 73), or a combination of these.
Note 4 to entry: Risk is often expressed in terms of a combination of the consequences of an event (including changes in circumstances) and the associated “likelihood” (as defined in ISO Guide 73) of occurrence.
3.8
process
set of interrelated or interacting activities that uses or transforms inputs to deliver a result
Note 1 to entry: Whether the result of a process is called output, product or service depends on the context of the reference.
3.9
competence
ability to apply knowledge and skills to achieve intended results
3.10
documented information
information required to be controlled and maintained by an organization (3.1) and the medium on which it is contained
Note 1 to entry: Documented information can be in any format and media, and from any source.
Note 2 to entry: Documented information can refer to:
—
the management system (3.4), including related processes (3.8);
—
information created in order for the organization to operate (documentation);
—
evidence of results achieved (records).
3.11
performance
measurable result
Note 1 to entry: Performance can relate either to quantitative or qualitative findings.
Note 2 to entry: Performance can relate to managing activities, processes (3.8), products, services, systems or organizations (3.1).
3.12
continual improvement
recurring activity to enhance performance (3.11)
3.13
effectiveness
extent to which planned activities are realized and planned results are achieved
3.14
requirement
need or expectation that is stated, generally implied or obligatory
Note 1 to entry: “Generally implied” means that it is custom or common practice for the organization (3.1) and interested parties (3.2) that the need or expectation under consideration is implied.
Note 2 to entry: A specified requirement is one that is stated, e.g. in documented information (3.10).
3.15
conformity
fulfilment of a requirement (3.14)
3.16
nonconformity
non-fulfilment of a requirement (3.14)
Note 1 to entry: A nonconformity is not necessarily a noncompliance (3.27).
3.17
corrective action
action to eliminate the cause(s) of a nonconformity (3.16) and to prevent recurrence
3.18
audit
systematic and independent process (3.8) for obtaining evidence and evaluating it objectively to determine the extent to which the audit criteria are fulfilled
Note 1 to entry: An audit can be an internal audit (first party) or an external audit (second party or third party (3.30)), and it can be a combined audit (combining two or more disciplines).
Note 2 to entry: An internal audit is conducted by the organization (3.1) itself, or by an external party on its behalf.
Note 3 to entry: “Audit evidence” and “audit criteria” are defined in ISO 19011.
Note 4 to entry: Independence can be demonstrated by the freedom from responsibility for the activity being audited or freedom from bias and conflict of interest.
3.19
measurement
process (3.8) to determine a value
3.20
monitoring
determining the status of a system, a process (3.8) or an activity
Note 1 to entry: To determine the status, there can be a need to check, supervise or critically observe.
3.21
governing body
person or group of persons that has the ultimate responsibility and authority for an organization’s (3.1) activities, governance and policies (3.5) and to which top management (3.3) reports and by which top management is held accountable
Note 1 to entry: Not all organizations, particularly small organizations, will have a governing body separate from top management.
Note 2 to entry: A governing body can include, but is not limited to, a board of directors, committees of the board, a supervisory board or trustees.
3.22
personnel
individuals in a relationship recognized as a work relationship in national law or practice, or in any contractual relationship that depends on its activity from the organization (3.1)
3.23
compliance function
person or group of persons with responsibility and authority for the operation of the compliance (3.26) management system (3.4)
Note 1 to entry: Preferably one individual will be assigned to the oversight of the compliance management system.
3.24
compliance risk
likelihood of occurrence and the consequences of noncompliance (3.27) with the organization’s (3.1) compliance obligations (3.25)
3.25
compliance obligations
requirements (3.14) that an organization (3.1) mandatorily has to comply with as well as those that an organization voluntarily chooses to comply with
3.26
compliance
meeting all the organization’s (3.1) compliance obligations (3.25)
3.27
noncompliance
non-fulfilment of compliance obligations (3.25)
3.28
compliance culture
values, ethics, beliefs and conduct (3.29) that exist throughout an organization (3.1) and interact with the organization’s structures and control systems to produce behavioural norms that are conducive to compliance (3.26)
3.29
conduct
behaviours and practices that impact outcomes for customers, employees, suppliers, markets and communities
3.30
third party
person or body that is independent of the organization (3.1)
Note 1 to entry: All business associates are third parties, but not all third parties are business associates.
3.31
procedure
specified way to carry out an activity or a process (3.8)
[SOURCE: ISO 9000:2015, 3.4.5]
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Bibliography
[1]
ISO 9000, Quality management systems — Fundamentals and vocabulary
[2]
ISO 9001, Quality management systems — Requirements
[3]
ISO 14001, Environmental management systems — Requirements with guidance for use
[4]
ISO 19011, Guidelines for auditing management systems
[5]
ISO 22000, Food safety management systems — Requirements for any organization in the food chain
[6]
ISO 26000, Guidance on social responsibility
[7]
ISO/IEC 27001, Information technology — Security techniques — Information security management systems — Requirements
[8]
ISO 31000, Risk management — Guidelines
[9]
IEC 31010, Risk management — Risk assessment techniques
[10]
ISO 37000, Guidance for the governance of organizations
[11]
ISO 37001, Anti-bribery management systems — Requirements with guidance for use
[12]
ISO 37002, Whistleblowing management systems — Guidelines
[13]
ISO Guide 73, Risk management — Vocabulary
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ICS 03.100.01; 03.100.02; 03.100.70
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