Universal Standards Assessment Forum

ISO/IEC 17021 – Management System Certification Bodies

Introduction

ISO/IEC 17021 is the internationally recognized standard that defines the requirements for bodies providing audit and certification of management systems. It ensures that certification bodies operate with competence, consistency, and impartiality when assessing organizations against standards such as ISO 9001, ISO 14001, ISO 45001, and others.

For an accreditation body such as Universal Standards Assessment Forum, ISO/IEC 17021 serves as the primary framework for evaluating and accrediting certification bodies. Accreditation to this standard demonstrates that a certification body has the capability to conduct audits in a reliable, transparent, and globally accepted manner, ensuring confidence in issued certificates.

The standard emphasizes impartial decision-making, auditor competence, structured audit processes, and effective management systems, forming the backbone of credible certification practices worldwide.

Key Requirements of ISO/IEC 17021

1. General Requirements

2. Structural Requirements

3. Resource Requirements

4. Information Requirements

5. Process Requirements

6. Management System Requirements

Accreditation Process for ISO/IEC 17021

For certification bodies seeking accreditation from Universal Standards Assessment Forum, the process typically includes:

  • Submission of application with scope of certification (e.g., ISO 9001, ISO 14001)
  • Provision of documented management system
  • Evaluation of policies, procedures, and records
  • Identification of gaps against ISO/IEC 17021-1 requirements
  • On-site or remote assessment of head office
  • Review of implementation of management system
  • Observation of certification body conducting an audit at client site
  • Evaluation of auditor competence and audit practices
  • Identification of nonconformities
  • Submission and verification of corrective actions
  • Independent review by accreditation committee
  • Granting of accreditation if requirements are fulfilled
  • Periodic surveillance assessments (usually annually)
  • Monitoring ongoing compliance
  • Full reassessment at defined cycle (typically every 3–5 years)

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