What is ISO 17025 Lead Implementer?
ISO/IEC 17025 is a critical international standard for testing and calibration laboratories, ensuring they operate competently and generate reliable results. Mastering this standard is essential for organisations seeking accreditation or striving for excellence in their laboratory operations. This training provides the tools and knowledge needed to implement and manage ISO 17025 effectively within an organisation.
Proficiency in ISO 17025 implementation is vital for laboratory managers, quality assurance professionals, and consultants who aim to enhance laboratory efficiency and maintain compliance with international standards. Professionals responsible for developing, implementing, or managing laboratory quality systems will benefit significantly from mastering the principles of ISO 17025.
This 3-day course offered by Oakwood International equips delegates with the practical knowledge and skills required to lead the implementation of ISO 17025 in laboratories. Through interactive sessions, real-world examples, and expert guidance, delegates will learn how to align laboratory practices with international standards, manage risks effectively, and achieve accreditation success.
Course Objectives:
- To understand the key requirements of ISO/IEC 17025
- To develop the skills needed to implement a laboratory management system
- To manage risks and ensure quality in laboratory operations
- To prepare for ISO 17025 accreditation assessments
- To create documentation and procedures aligned with ISO 17025
- To foster continuous improvement in laboratory practices
- To lead a team in adopting ISO 17025 principles effectively
Upon completion, delegates will receive a certification from Oakwood International, validating their expertise in ISO 17025 implementation. This credential enhances professional credibility and demonstrates the ability to lead laboratories towards operational excellence and compliance.
Course Outline
ISO 17025 Lead Implementer
Module 1: Introduction to ISO 17025
- ISO 17025
Module 2: Requirements of ISO 17025
- Overview
Module 3: ISO 19011 Relationship to ISO 17025
- ISO 19011
- ISO 17025
Module 4: Scope
- Overview
Module 5: Normative References
- Introduction to Normative References
Module 6: Terms and Definitions
- Overview
Module 7: General Requirements
- Overview
- Impartiality
- Confidentiality
Module 8: Structural Requirements
- Overview of Structural Requirements
Module 9: Resource Requirements
- Introduction
- General
- Personnel
- Facilities and Environmental Conditions
- Equipment
- Metrological Traceability
- Externally Provided Products and Services
Module 10: Process Requirements
- Introduction to Process Requirements
- Review - Requests, Tenders, and Contracts
- Selection, Verification, and Validation of Methods
- Sampling
- Handling Test or Calibration Items
- Technical Records
- Evaluation of Measurement Uncertainty
- Ensure Results Validity
- Reporting of Results
- Complaints
- Nonconforming Work
- Control of Data and Information Management
Module 11: Management System Requirements
- Options
- Option A
- Option B
- General
Module 12: Management System Documentation
- Overview
- Document Categories
Module 13: Control Management System Documents
- Overview
- Primary Document Control Requirements in the ISO 17025 Standard
Module 14: Control of Records
- Overview
Module 15: Address Risks and Opportunities
- Overview of Address Risks and Opportunities
Module 16: Improvement
- Overview of Improvement
Module 17: Corrective Actions
- Steps to Take Corrective Actions
Module 18: Internal Audit and Management Reviews
- Internal Audit
- Management Reviews
Module 19: Terminology – ISO 9000, VIM etc.
- ISO 9000 Terminology in English
- What is ISO 9000?
- Common ISO Definitions
Module 20: Fundamental Audit Concepts and Principles
- Overview
Module 21: Auditing Requirements and Assessment: ISO 17011:2017, ISO 19011:2018
- Auditing: ISO 17011:2017
- Auditing: ISO 19011:2018
Module 22: Recognition and Oversight of ILAC, IAAC, APAC etc.
- Description of ILAC
- ILAC’s Global Role
- Abbreviations
- ILAC Documents
- ILAC P10 Traceability Policy
Module 23: Test Reports, AB Symbols, Equipment Stickers, and Certificates
- AB Symbols
- Certificates
- Certificate Naming Convention
Module 24: Clauses 4, 5, and 6 Review
- Clause 4: General Requirements
- Clause 5: Structural Requirements
- Clause 6: Resource Requirements
Module 25: Clauses 7 and 8 Review
- Clause 7: Process Requirements
- Clause 8: Option
Module 26: Guidelines for Auditing: ISO 19011
- ISO 19011 Auditing Guidelines
- What is ISO 19011?
- Standard Facts of ISO 19011
- Who ISO 19011:2018 should be Used?
- What does ISO 19011:2018 Accomplish?
Module 27: GUM (Uncertainty), PT/ILC, and Traceability
- GUM (Uncertainty)
- PT/ILC
- Traceability
Module 28: Opening and Closing Meeting Activities
- Opening Meeting
- What Happens in an Opening Meeting?
- Closing Meeting
- What Happens in a Closing Meeting?
- What Happens in a Closing Meeting?
Module 29: ISO 19011 Relationship to ISO 17025
- ISO 19011
- ISO 17025
Module 30: Auditing Technical Methods
- Overview
Module 31: Reporting Audit Results
- Internal Audit Report
Module 32: Audit Checklists
- ISO 17025:2017 Audit Checklist for Laboratory Accreditation System Requirements
- Content of ISO/IEC 17025:2017 Audit Checklists
Module 33: Review of Standards and Internal Auditing Issues
- Review of Standards
- Internal Auditing Issues
Module 34: Introduction to Lab Management System (LMS)
- Standard and Regulatory Framework
- Laboratory Management System
- Laboratories and Accreditation Principles
- Testing and Calibration Concepts
- Identifying the Objective and Scope
- Understanding Organisation
- Analysing Existing System
Module 35: Planning LMS Implementation
- Leadership and LMS Project Approval
- Laboratory Policies
- Document Management Process
Module 36: Implementing LMS
- Design of Controls
- Drafting of Specific Policies and Procedures
- Communication Planning
- Training and Awareness Planning
- Resource Management
- Customer Management
- Operations Management
Module 37: Monitoring, Measurement, and Continuous Improvement
- Monitoring, Analysis, and Evaluation
- Treating Problems and Nonconformities
- Continual Improvement
- Accreditation Preparation
- Implementers Evaluation
Included
Included
- No course includes are available.
Offered In This Course:
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Video Content
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eLearning Materials
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Study Resources
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Completion Certificate
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Tutor Support
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Interactive Quizzes
Learning Options
Discover a range of flexible learning options designed to meet your needs. Select the format that best supports your personal growth and goals.
Online Instructor-Led Training
- Live virtual classes led by experienced trainers, offering real-time interaction and guidance for optimal learning outcomes.
Online Self-Paced Training
- Flexible learning at your own pace, with access to comprehensive course materials and resources available anytime, anywhere.
Build your future with Oakwood International
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Frequently Asked Questions
Q. What is the ISO 17025 Lead Implementer Course?
The course trains delegates to
implement and manage ISO/IEC 17025, an international standard for the
competence of testing and calibration laboratories.
Q. Who should attend this training?
This training is ideal for Laboratory
Managers, Quality Assurance Professionals, Consultants, and individuals
responsible for implementing ISO 17025 systems.
Q. Will I receive a certificate upon completion?
Yes, delegates receive a certificate
that validates their knowledge and skills in ISO 17025 implementation.
Q. Why is ISO 17025 important?
ISO 17025 ensures laboratory
competence, reliable results, and global recognition, making it essential for
laboratories aiming for accreditation.
Q. What skills will I gain from this course?
Delegates will learn to implement ISO
17025 systems, manage risks, ensure compliance, and lead teams towards
accreditation.