When a food safety management system receives certification, consumers, regulators, and business partners trust that the organization truly meets the required standards. But who ensures that the certification bodies themselves are competent, impartial, and consistent? That’s where ISO/IEC 17021:2006 comes in. This international standard sets rigorous requirements for bodies that audit and certify management systems, establishing a foundation of trust in the entire certification process.

Table of Contents

What is ISO/IEC 17021:2006?

ISO/IEC 17021:2006 is an international standard that specifies requirements for the competence, consistency, and impartiality of bodies providing audit and certification services for management systems. Whether it’s a quality management system under ISO 9001, an environmental management system under ISO 14001, or a food safety management system under ISO 22000, certification bodies must comply with this standard to ensure their certifications are credible and reliable.

The standard applies specifically to third-party conformity assessment bodies-organizations that provide independent certification services. These certification bodies do not need to offer all types of management system certification, but whatever certifications they do provide must meet the requirements outlined in ISO/IEC 17021:2006.

Core principles that build trust

ISO/IEC 17021:2006 is built on six fundamental principles that ensure certification bodies operate with integrity and inspire confidence in their work.

Impartiality

Certification bodies must remain independent and objective, avoiding any conflicts of interest that could influence their certification decisions. The standard recognizes that certification bodies receive revenue from clients seeking certification, which creates a potential threat to impartiality. To address this, certification bodies must identify and manage all risks to impartiality through documented procedures and organizational structures. They cannot provide both certification and consulting services to the same client for the same management system.

Competence

Certification bodies must employ auditors and personnel with appropriate education, work experience, audit training, and expertise for the management systems they certify. This ensures that when an auditor evaluates a food safety management system in a processing facility, they understand both the requirements of the standard and the specific operational context of food production. The standard requires systems for assessing, monitoring, and continuously improving personnel competence.

Responsibility

Certification bodies bear full responsibility for their certification decisions and audit results. They must clearly define the responsibilities and authority of all personnel involved in the certification process, from auditors conducting on-site evaluations to decision-makers granting certificates.

Openness

Transparency is essential for building confidence. Certification bodies must be open about their policies, procedures, and certification processes. Information about how certification works should be publicly accessible, helping organizations understand what to expect when seeking certification.

Confidentiality

While openness is important, certification bodies must also protect sensitive business information obtained during audits. Strict confidentiality procedures ensure that proprietary information, audit findings, and organizational data remain secure and are only accessed by authorized personnel.

Responsiveness to complaints

Effective complaint handling protects both the certification body and its clients. Certification bodies must have documented procedures for addressing complaints and appeals, ensuring that concerns are investigated fairly and resolved transparently. This provides an important safeguard against errors or unreasonable behavior.

Structural and organizational requirements

ISO/IEC 17021:2006 establishes specific requirements for how certification bodies must be structured and operated.

Certification bodies must be legally identifiable entities with clear contractual agreements that specify the responsibilities of all parties involved. They must have adequate liability coverage and financial resources to operate effectively and cover potential liabilities.

Management of impartiality

One of the most critical structural requirements is the establishment of an impartiality committee. This committee safeguards the objectivity of certification decisions by providing oversight and including balanced representation from various stakeholder groups-such as clients, customers of certified organizations, regulatory bodies, and industry associations. The committee reviews potential conflicts of interest and ensures that commercial or financial pressures do not compromise certification integrity.

Non-discriminatory conditions

Certification bodies must offer their services fairly to all applicants without discrimination. Access to certification should not depend on the size of the organization or its affiliations.

Resource requirements: competent personnel

The quality of certification depends heavily on the people conducting audits and making certification decisions. ISO/IEC 17021:2006 mandates that certification bodies have rigorous processes for selecting, training, and evaluating personnel.

Auditors must possess specific qualifications including relevant education, work experience in the field they’re auditing, formal audit training, and documented audit experience. For specialized areas like food safety, auditors need both technical knowledge of food production processes and understanding of applicable standards.

Certification bodies must maintain records of personnel competence and provide ongoing training to keep auditors current with evolving standards and industry practices. They must also monitor auditor performance through techniques such as witnessing audits and reviewing audit reports.

Outsourcing considerations

If certification bodies outsource any audit or certification activities, they remain fully responsible for those activities. They must ensure that outsourced personnel meet the same competence, impartiality, and confidentiality requirements as their own staff.

Process requirements: the certification journey

ISO/IEC 17021:2006 outlines specific requirements for the certification process itself, from initial application through ongoing surveillance.

Initial certification

The certification process typically begins with an application review where the certification body evaluates whether it has the competence to audit the organization’s management system. Initial certification involves a two-stage audit process.

Stage 1 focuses on reviewing the organization’s documentation and readiness for certification. Auditors assess whether the management system documentation meets standard requirements, review internal audit and management review processes, and plan the Stage 2 audit based on their findings.

Stage 2 is the comprehensive on-site audit where auditors evaluate whether the management system is effectively implemented and achieving its intended objectives. They examine processes, interview personnel, review records, and verify that practices align with documented procedures.

Certification decisions

After completing the audit, only designated personnel who were not involved in conducting the audit make certification decisions. This separation ensures objectivity. If nonconformities are identified, the organization must implement corrections and corrective actions before certification can be granted.

Maintaining certification

Certification is not a one-time achievement. Organizations must undergo surveillance audits throughout the certification cycle to ensure ongoing compliance. These audits assess whether the management system continues to meet requirements and verify that previous nonconformities have been effectively addressed. Certification bodies must also have procedures for suspending, withdrawing, or reducing the scope of certification when organizations fail to maintain compliance.

Management system requirements for certification bodies

In a requirement that exemplifies “practice what you preach,” ISO/IEC 17021:2006 requires certification bodies to implement their own management systems. These systems must include documented policies, procedures, and processes that support the consistent delivery of certification services.

The certification body’s management system should address document control, record keeping, management review, internal audits, corrective actions, and continual improvement. This ensures that certification bodies maintain the same level of systematic management they evaluate in their clients.

The impact on trust and international trade

ISO/IEC 17021:2006 has significant implications for global commerce and public confidence. By establishing internationally harmonized requirements, the standard facilitates recognition of certification bodies across borders. When a food manufacturer in one country receives certification from an accredited certification body, trading partners and regulators in other countries can trust that the certification meets consistent, rigorous standards.

The standard replaced earlier ISO/IEC Guides 62 and 66, distilling international consensus on best practices and incorporating guidance from the International Accreditation Forum. This harmonization helps increase awareness of and confidence in certification bodies, supporting international trade and reducing the need for multiple certifications in different markets.

Accreditation to ISO/IEC 17021:2006

Many certification bodies seek accreditation to demonstrate their compliance with ISO/IEC 17021:2006. Accreditation bodies assess certification bodies against the standard’s requirements through comprehensive evaluations including documentation review, office assessments, and witnessing of actual audits. This third-party verification provides an additional layer of assurance that certification bodies operate competently and impartially.

What do you think? How important is it to verify that your certification body is accredited to ISO/IEC 17021:2006? Does understanding the rigor behind certification processes change how you view management system certifications in your organization?

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References
  1. https://www.iso.org/standard/29343.html
  2. https://www.jasanz.org/stories/iso-iec-17021-1
  3. https://www.bsigroup.com/en-IE/products-and-services/standards/isoiec-17021-series-requirements-for-bodies-auditing-management-systems/

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Food Safety and Quality Management Systems

1 Introduction to Management systems

  1. Introduction to ISO 9001
  2. ISO 9000
  3. Introduction to ISO 14001:2004
  4. How to Use ISO 14001
  5. Introduction to OHSAS 18001:2007
  6. How to Use OHSAS 18001:2007
  7. Introduction to ISO/IEC 27001
  8. The PDCA Model

2 Auditing

  1. Clause 1 – Scope of the Standard
  2. Clause 2 – Normative References
  3. Clause 3 – Terms and Definitions
  4. Clause 4 – Principles of Auditing
  5. Clause 5 – Managing an Audit Program
  6. Clause 6 – Audit Activities
  7. Clause 7 – Competence and Evaluation of Auditors

3 Standardization and Accreditation

  1. International Accreditation Forum (IAF)
  2. International Laboratory Accreditation Cooperation (ILAC)
  3. Quality Council of India (QCI)
  4. National Accreditation Board for Testing and Calibration Laboratories (NABL)
  5. ISO/TS 22003:2007 Food Safety Management System
  6. ISO Guide 65: General Requirements for Bodies Operating Product Certification Systems
  7. ISO/IEC 17020:1998 General Criteria for the Operation of Various Types of Bodies Performing Inspections
  8. ISO/IEC 17021:2006 – Conformity Assessment-Requirements for Bodies Providing Audit and Certification of Management Systems
  9. ISO 17025:2005 General Requirements for the Competence of Testing and Calibration Laboratories

4 ISO 9001-2000 – An Overview

  1. ISO 9000
  2. Quality Management Principles
  3. ISO 9000:2005, Quality Management Systems: Fundamentals and Vocabulary
  4. ISO 9001:2000, Quality Management Systems: Requirements
  5. Steps for Implementing Quality Management Systems
  6. Benefits of ISO 9001:2000
  7. ISO 9004:2000, Quality Management Systems: Guidelines for Performance Improvements
  8. Relationship with ISO 9001:2000
  9. Self-assessment Model

5 ISO 9001-2000 – Structure

  1. Documentation Structure of ISO 9001:2000
  2. Quality Manual
  3. Mandatory Procedures
  4. Standard Operating Procedures (SOPs)
  5. Process Definition Documents
  6. Work Instructions
  7. Miscellaneous Documents
  8. Formats and Records
  9. ISO 9001:2000 Clauses

6 Clause wise interpretation of ISO 9001-2000

  1. Clause 1: Scope
  2. Clause 2: Normative Reference
  3. Clause 3: Terms and Definitions
  4. Clause 4: Quality Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Product Realization
  8. Clause 8: Measurement, Analysis and Improvement

7 ISO 9001-2000 – Case Studies

  1. Engineering Job Work Organisation
  2. Software Development Organisation
  3. Management Review in Engineering
  4. Customer-Related Processes in Software
  5. Internal Audits in Engineering
  6. Design and Development in Software
  7. Corrective and Preventive Actions in Software
  8. Customer Property Management in Engineering

8 ISO 22000-2005 – An Overview

  1. What Does ISO 22000 Bring to the HACCP Method?
  2. System Components
  3. Communication between Participants in the Food Industry
  4. ISO 22000: A Passport for Exporting?
  5. Why do Companies Commit themselves to an ISO 22000 Approach?
  6. Who Should Use ISO 22000:2005?
  7. Why Use ISO 22000:2005?
  8. ISO 22000 and HACCP
  9. Codex Alimentarius
  10. Key Elements and Benefits of ISO 22000

9 ISO 22000-2005 – Structure

  1. Economic Loss due to Food Borne Illness
  2. ISO 22000: 2005 Clauses
  3. FSMS Documentation Structure
  4. Food Safety Team Structure
  5. Food Safety Manual
  6. Mandatory Procedures
  7. Standard Operating Procedures (SOP)/Work Instructions
  8. HACCP Pre-steps Related Documents
  9. HACCP Principles Related Documents
  10. Miscellaneous Documents
  11. Formats and Records

10 Clause-wise interpretation of ISO 22000- 2005

  1. Clause 1: Scope
  2. Clause 2: Normative References
  3. Clause 3: Terms and Definitions
  4. Clause 4: Food Safety Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Planning and Realization of Safe Products
  8. Clause 8: Validation, Verification and Improvement of the FSMS

11 ISO 22000-2005-Case Studies

  1. Kick-off meeting
  2. Introduction to the standard
  3. Formation of food safety team
  4. Description of product and its intended use
  5. PRP (Pre-requisite programme)
  6. Flow diagrams, process steps and control measures
  7. Control measure assessment
  8. Verification of food safety management system
  9. Traceability system
  10. External communication
  11. Internal communication
  12. Management Reviews

12 An Overview and Requirements of ISO 17025

  1. Introduction to the ISO/IEC 17025 Standard
  2. Scope of ISO/IEC 17025
  3. Normative References
  4. Terms and Definitions
  5. General Requirements
  6. Structural Requirements
  7. Resource Requirements
  8. Process Requirements
  9. Management System Requirements

13 Requirements specific to Food testing laboratories – Physical and chemical Parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Chemical and Physical Testing Requirements of Food Products
  4. Laboratory Quality Management System
  5. Management Requirements (Clause 4 of ISO 17025)
  6. Technical Requirements (Clause 5 of ISO 17025)
  7. Traceability of Measurement
  8. Sampling
  9. Handling Test and Calibration Items
  10. Assuring the Quality of Test and Calibration Results

14 Requirements specific to Food testing laboratories – Biological parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Biological Testing Requirements of Food Products

15 General topics- related to Food testing laboratories

  1. Method Validation
  2. Ruggedness
  3. Uncertainty of Measurement
  4. International Accreditation Aspects

16 BRC Food and BRC/IOP Standards – An Overview

  1. BRC Global Standard – Food (Issue 5, January 2005)
  2. Introduction to BRC Food Standard
  3. Legislative Requirements
  4. Benefits of the BRC Global Standard – Food
  5. Principles of the BRC Global Standard – Food
  6. The Standard Technical Advisory Committee
  7. Scope of the BRC Global Standard – Food
  8. The Format of the BRC Global Standard – Food
  9. Application
  10. Structure and Interpretation of the Standard
  11. BRC / IOP Global Standard Issue 3 2001 (Food Packaging and Other Packaging Materials)
  12. IOP: The Institute of Packaging
  13. BRC/IOP Relationship
  14. Benefits of BRC/IOP Packaging Standard
  15. Principles of BRC/IOP Packaging Standard
  16. Application
  17. Structure of BRC / IOP Global Standard – Food Packaging and Other Packaging Materials

17 International Food Standard

  1. Background of the IFS
  2. Service Protocol of the IFS ISSUE 5
  3. Contractual Arrangements – Selection of Certifying Body
  4. Audit Notification
  5. Scope of the Audit
  6. Audit Flow – Preparing the Audit Plan
  7. Level Determination – KO, Major NC’s, NA
  8. Scores, Issuing the Audit Report and Certification
  9. Audit Frequency
  10. Audit Report
  11. Awarding of Certificate
  12. Distribution of the Audit Report
  13. Supplementary Action
  14. Appeal Procedure
  15. Complaints
  16. IFS – Catalogue of Requirements
  17. Management of Quality System
  18. Management Responsibility
  19. Resource Management
  20. Product Realization
  21. Measurements, Analysis and Improvements
  22. Requirements for Certification Bodies and Auditors
  23. Report

18 SQF 1000 And SQF 2000

  1. SQF 1000
  2. Interpretation of SQF 1000 Standard
  3. SQF 2000
  4. Interpretation of SQF 2000 Standard
  5. Let Us Sum Up

19 Global GAP and India GAP

  1. Potential Benefits and Challenges Related to Good Agricultural Practices (GAP)
  2. Description of the FAO/GAPs
  3. USDA GAP/GHP Programme
  4. Global GAP
  5. India GAP