HomeServicesTOTAL QUALITY MANAGEMENT (TQM) & BUSINESS EXCELLENCELaboratory Quality Management System ISO 17025:2017

Laboratory Quality Management System ISO 17025:2017

ISO/IEC 17025:2017

Duration: 1 Days

Ever Better Solutions (EBS) offers a structured and practical training program on ISO/IEC 17025:2017, the internationally recognized standard for the competence of testing and calibration laboratories. This standard is used globally by accreditation bodies to assess laboratory capability and ensure reliability of test and calibration results.

The 2017 revision introduced significant updates including risk-based thinking, alignment with modern quality management principles, improved process approach, and enhanced technical requirements. Our 2-day intensive program is designed to build strong understanding and practical implementation skills to help laboratories achieve and maintain accreditation.

Why ISO/IEC 17025:2017 Matters

ISO/IEC 17025:2017 strengthens laboratory credibility, enhances customer confidence, and improves operational control. It ensures:

  • Technical competence of laboratory personnel
  • Reliable and traceable test results
  • Effective risk management practices
  • Robust documentation and process control
  • International recognition through accreditation

Training Objectives

This training enables participants to:

  • Understand the structure and key requirements of ISO/IEC 17025:2017
  • Identify major changes from the 2005 version
  • Apply risk-based thinking in laboratory operations
  • Develop and structure laboratory documentation
  • Conduct effective internal audits
  • Prepare for accreditation assessments

Course Modules

1. Introduction & Background
  • Basic Concepts of Quality
  • National and International Importance of Accreditation
  • Evolution of ISO/IEC 17025
  • Key Changes in the 2017 Version
2. Standard Requirements Overview
  • Scope and Normative References
  • Terms and Definitions
  • General Requirements
3. Risk Management & Documentation
  • Risk Identification and Control Techniques
  • Quality Manual and Procedure Development
  • Control of Documented Information
4. Internal Audit & Accreditation Process
  • Types and Phases of Internal Audits
  • Audit Planning and Execution
  • Accreditation Process Overview
5. Technical & Management System Requirements
  • Structural Requirements
  • Resource Requirements
  • Process Requirements
  • Management System Requirements

Who Should Attend?

  • Laboratory Managers
  • QA/QC Managers
  • Technical Managers
  • Laboratory Personnel
  • Management Representatives
  • Documentation Officers
  • Internal Auditor Candidates
  • Laboratories transitioning from ISO/IEC 17025:2005 to 2017

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