ISO 17025 Training

Online Instructor-led (1 days)

Classroom (1 days)

Online Self-paced (8 hours)

ISO 17025 Foundation Training Course Outline

This course covers the following topics:

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

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Who should attend this ISO 17025 Foundation Course?

The ISO 17025 Foundation Course is designed to provide delegates with a foundational understanding of the ISO 17025 standard, which specifies the general requirements for the competence of testing and calibration laboratories. It can benefit a wide range of professionals, including:

  • Laboratory Technicians
  • Quality Assurance Professionals
  • Laboratory Managers and Supervisors
  • Quality Control Specialists
  • Regulatory Compliance Officers
  • Auditors
  • Training and Development Specialists

Prerequisites of the ISO 17025 Foundation Training Course

There are no formal prerequisites for this ISO 17025 Foundation Course.

ISO 17025 Foundation Training Course Overview

ISO 17025 Foundation Training provides a comprehensive introduction to the principles and requirements of ISO/IEC 17025, focusing on the general aspects of laboratory testing and calibration. This international standard sets out the criteria for the competence of testing and calibration laboratories, ensuring reliability and accuracy in their results. Understanding ISO 17025 is crucial for laboratories seeking accreditation and for professionals involved in quality assurance and compliance.

To meet industry standards and regulatory requirements, professionals across various fields, including laboratory managers, technicians, and quality assurance personnel, should aim at mastering ISO 17025. This knowledge is essential for ensuring the reliability and accuracy of testing and calibration processes, ultimately enhancing the credibility of laboratory results.

This 1-day ISO 17025 Foundation Training provided by The Knowledge Academy, delves into the practical aspects of ISO/IEC 17025 implementation, offering real-world examples and case studies. Delegates will have the opportunity to engage in interactive discussions, gaining insights from experienced trainers who bring a wealth of practical knowledge to the session.

Course Objectives:

  • To comprehend the fundamental principles and requirements of ISO/IEC 17025
  • To identify the key elements of laboratory testing and calibration processes
  • To understand the importance of documentation and quality control in laboratories
  • To grasp the significance of competence, impartiality, and confidentiality in testing and calibration
  • To learn how to implement ISO 17025 standards in a laboratory setting
  • To prepare for accreditation and compliance audits effectively

Upon completion of this course, delegates will gain a solid understanding of ISO/IEC 17025 and its application in laboratory settings. Armed with this knowledge, they will be better equipped to ensure the quality, reliability, and compliance of testing and calibration processes, thereby enhancing the overall efficiency and credibility of their laboratories.

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What’s included in this ISO 17025 Foundation Course?

  • World-Class Training Sessions from Experienced Instructors 
  • ISO 17025 Foundation Certificate
  • Digital Delegate Pack

Show moredown

Online Instructor-led (5 days)

Classroom (5 days)

Online Self-paced (40 hours)

ISO 17025 Lead Auditor Exam

ISO 17025 Lead Auditor Training Course Outline

Module 1: Introduction to ISO 17025

Module 2: Requirements of ISO 17025

Module 3: The Relationship between ISO 19011 and ISO 17025

Module 4: Scope

Module 5: Normative References

Module 6: Terms and Definitions

Module 7: General Requirements

  • Impartiality
  • Confidentiality

Module 8: Structural Requirements

Module 9: Resource Requirements

  • General
  • Personnel
  • Facilities and environmental conditions
  • Equipment
  • Metrological traceability
  • Externally provided products and services

Module 10: 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
  • Ensuring result validity
  • Reporting of results
  • Complaints
  • Nonconforming work
  • Control of data and information management

Module 11: Management System Requirements

  • Options
  • General
  • Option A
  • Option B

Module 12: Management System Documentation

Module 13: Control Management System Documents

Module 14: Control of Records

Module 15: Address Risks and Opportunities

Module 16: Improvement

Module 17: Corrective Actions

Module 18: Management Reviews

Module 19: Terminology – ISO 9000, VIM etc.

Module 20: Fundamental Audit Concepts and Principles

Module 21: Auditing Requirements and Assessment: ISO 17011:2004, ISO 19011:2011

Module 22: Recognition and Oversight of ILAC, IAAC, APLAC

Module 23: Test Reports, AB Symbols, Equipment Stickers, Certificates

Module 24: Clauses 4, 5, and 6 Review

  • Case studies on clauses 4, 5 and 6

Module 25: Clauses 7 and 8 Review

  • Case studies on clauses 7 and 8

Module 26: Guidelines for Auditing: ISO 19011

Module 27: GUM (Uncertainty), PT/ILC, Traceability

Module 28: Opening and Closing Meeting Activities

Module 29: Auditing Technical Methods

Module 30: Reporting Audit Results

Module 31: Audit Checklists and Audit Reports

Module 32: Review of Standards and Internal Auditing Issues

Module 33: Introduction to Lab Management System (LMS)

  • Standards and regulatory frameworks
  • Laboratory management systems
  • Laboratories and accreditation fundamental principles
  • Testing and calibration concepts
  • Implementation of LMS
  • Understanding the organisation
  • Analysing existing systems

Module 34: Planning LMS Implementation

  • Leadership and LMS project approval
  • Scope of LMS
  • Laboratory policies
  • Organisational structure
  • Document management process

Module 35: Implementing an LMS

  • Design of controls
  • Drafting of specific policies and procedures
  • Communication planning
  • Training and awareness planning
  • Resource management
  • Customer management
  • Operations management

Module 36: LMS Monitoring, Measurement, and Continuous Improvement

  • Monitoring, analysis, and evaluation
  • Treating problems and nonconformities
  • Continual improvement
  • Accreditation preparation
  • Implementers evaluation

Module 37: Planning an ISO 17025 Audit

  • Audit approach
  • Preparing the ISO 17025 Audit
  • Conducting an opening meeting

Module 38: Conducting the ISO 17025 Audit

  • Communication during audit
  • Audit procedures
    • Observation
    • Document review
    • Interview
    • Sampling techniques
    • Technical verification
    • Corroboration and evaluation
  • Audit test plans
  • Formulation of audit findings
  • Documenting nonconformities

Module 39: Concluding and Follow-Up of ISO 17025 Audits

  • Audit documentation
  • Quality review
  • Closing meeting
  • Evaluation of corrective action plans
  • ISO 17025 surveillance audits
  • ISO 17025 internal audit management program

Show moredown

Who should attend this ISO 17025 Lead Auditor Course?

The ISO 17025 Lead Auditor Course is a course designed to provide professionals with the knowledge to lead and conduct audits of testing and calibration laboratories in accordance with the ISO 17025 standards. This course can be beneficial to a wide range of professionals, including:

  • Lead Auditors
  • Quality Managers
  • Laboratory Managers
  • Quality Assurance Officers
  • Technical Experts
  • Auditors
  • Process Improvement Professionals
  • Consultants

Prerequisites of the ISO 17025 Lead Auditor Training Course

There are no formal prerequisites for this ISO 17025 Lead Auditor Course.

ISO 17025 Lead Auditor Training Course Overview

ISO 17025 Lead Auditor Training holds significant relevance in the context of international standards for testing and calibration laboratories. The ISO 17025 standard ensures that these laboratories maintain a high level of quality, competence, and consistency in their operations. With the increasing demand for reliable and accurate results across diverse industries such as healthcare, environmental monitoring, and manufacturing, adherence to ISO 17025 has become paramount. 

For professionals aiming to master ISO 17025, the importance lies in their ability to enhance and ensure the quality of laboratory processes. Individuals in roles such as Quality Managers, Laboratory Supervisors, and Auditors play a crucial role in upholding standards and compliance. This ISO 17025 Training enables them to conduct effective audits that identify areas of improvement, nonconformities, and potential risks.

The 5-day ISO 17025 Training by The Knowledge Academy equips delegates with essential skills to lead ISO 17025 audits effectively. Covering key concepts and audit techniques, it provides a comprehensive understanding of the standard, enabling professionals to contribute significantly to laboratory quality assurance. This course will be conducted by our highly experienced trainers.

Course Objectives:

  • To comprehend the fundamentals of ISO 17025 and its application in laboratory settings
  • To gain insights into auditing principles, techniques, and practices
  • To understand the role and responsibilities of a Lead Auditor
  • To learn how to plan, conduct, and report on ISO 17025 audits
  • To identify nonconformities and recommend corrective actions
  • To enhance communication and interpersonal skills for effective auditing

Upon completion of this course, delegates will possess the expertise to lead ISO 17025 audits, ensuring adherence to international standards and enhancing the overall quality and reliability of laboratory testing and calibration processes. This proficiency will open doors to career advancement and contribute to organisational excellence

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What’s included in this ISO 17025 Lead Auditor Course?

  • ISO 17025 Lead Auditor Examination
  • World-Class Training Sessions from Experienced Instructors 
  • ISO 17025 Lead Auditor Certificate
  • Digital Delegate Pack

Show moredown

ISO 17025 Lead Auditor Exam Information

To achieve the ISO 17025 Lead Auditor, candidates will need to sit for an examination. The exam format is as follows: 

  • Question Type: Multiple Choice  
  • Total Questions: 30 
  • Total Marks: 30 Marks 
  • Pass Mark: 50%, or 15/30 Marks 
  • Duration: 40 Minutes  
  • Open Book/ Closed Book: Closed Book

Show moredown

Online Instructor-led (3 days)

Classroom (3 days)

Online Self-paced (24 hours)

ISO 17025 Lead Implementer Exam

ISO 17025 Lead Implementer Training Course Outline

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?

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

Show moredown

Who should attend this ISO 17025 Lead Implementer Training Course?

The ISO 17025 Lead Implementer Course is designed to equip professionals with the knowledge and skills required to lead the implementation of a laboratory Quality Management System based on the ISO 17025 standard. This course can be beneficial to a wide range of professionals, including:

  • Laboratory Directors and Managers
  • Quality Managers
  • Technical Managers
  • Quality Assurance Officers
  • Procurement Managers
  • Compliance Officers
  • Internal Auditors
  • Consultants

Prerequisites of the ISO 17025 Lead Implementer Training Course

There are no formal prerequisites for this ISO 17025 Lead Implementer Course.

ISO 17025 Lead Implementer Training Course Overview

Among the ISO 17025 Training Courses, the ISO 17025 Lead Implementer Training is designed to provide delegates with a thorough understanding of the international standard for testing and calibration laboratories. This standard, ISO/IEC 17025, outlines the requirements for competence, impartiality, and consistent operation in laboratories, ensuring reliable results and data.

It is crucial for professionals to master ISO 17025 as it serves as a benchmark for demonstrating competence and reliability in laboratory operations. Laboratory Managers, Quality Assurance Personnel, and professionals responsible for ensuring accurate test and calibration results should aim to acquire in-depth knowledge of ISO/IEC 17025 to enhance their organisations' credibility and compliance with international standards.

This 3-day training by the Knowledge Academy aims to equip delegates with the essential skills and knowledge needed to implement and maintain ISO/IEC 17025 standards effectively. The course covers key aspects such as management system requirements, documentation, and auditing, providing a practical and hands-on approach to mastering the implementation of ISO 17025.

Course Objectives:

  • To understand the principles and requirements of ISO/IEC 17025
  • To gain insights into the documentation and management system requirements
  • To learn effective strategies for implementing ISO 17025 in a laboratory setting
  • To acquire auditing skills for assessing compliance with ISO 17025 standards
  • To identify potential challenges and best practices for successful implementation
  • To ensure delegates are well-prepared to lead ISO 17025 implementation efforts in their organisations

Upon completion of this course, delegates will be equipped with the knowledge and skills needed to implement ISO/IEC 17025 effectively, enhancing the quality and reliability of laboratory operations. They will be better positioned to lead their organisations in achieving and maintaining compliance with international standards, ultimately contributing to improved confidence in testing and calibration results.

Show moredown

What’s included in this ISO 17025 Lead Implementer Course?

  • ISO 17025 Lead Implementer Examination
  • World-Class Training Sessions from Experienced Instructors 
  • ISO 17025 Lead Implementer Certificate
  • Digital Delegate Pack

Show moredown

ISO 17025 Lead Implementer Exam Information

To achieve the ISO 17025 Lead Implementer, candidates will need to sit for an examination. The exam format is as follows: 

  • Question Type: Multiple Choice  
  • Total Questions: 30 
  • Total Marks: 30 Marks 
  • Pass Mark: 50%, or 15/30 Marks 
  • Duration: 40 Minutes  
  • Open Book/ Closed Book: Closed Book

Show moredown

Online Instructor-led (2 days)

Classroom (2 days)

Online Self-paced (16 hours)

ISO 17025 Internal Auditor Exam

ISO 17025 Internal Auditor​ Training Course Outline

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?

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

Show moredown

Who should attend this ISO 17025 Internal Auditor Training Course?

The ISO 17025 Internal Auditor Course is designed to provide delegates with a foundational understanding of the ISO 17025 standard, which is used to audit testing and calibration laboratories. It can benefit a wide range of professionals, including:

  • Laboratory Managers
  • Quality Managers
  • Laboratory Accreditation Specialists
  • Quality Control Specialists
  • Regulatory Compliance Officers
  • Internal Auditors
  • Consultants

Prerequisites of the ISO 17025 Internal Auditor Training Course

To attend this training course, delegates must have a foundational understanding of ISO 17025. For this knowledge, we suggest completing our ISO 17025 Foundation Course.

ISO 17025 Internal Auditor Training Course Overview

The ISO 17025 Internal Auditor Training focuses on developing the skills necessary to conduct internal audits in laboratories, ensuring they comply with the ISO/IEC 17025 standard. This standard outlines the general requirements for the competence of testing and calibration laboratories, emphasising the importance of quality management systems in these settings.

Professionals engaged in laboratory operations, quality assurance, or those responsible for ensuring compliance with ISO/IEC 17025 should aim at mastering this subject. A solid understanding of internal auditing is essential for maintaining the integrity and reliability of testing and calibration processes within laboratories.

The 2-day training by the Knowledge Academy provides delegates with the knowledge and practical insights required to perform effective internal audits in accordance with ISO/IEC 17025. The course covers key concepts, audit methodologies, and best practices, empowering delegates to contribute significantly to the enhancement of their laboratory's quality management system.

Course Objectives:

  • To comprehend the principles and requirements of ISO/IEC 17025
  • To understand the role and responsibilities of an Internal Auditor
  • To gain proficiency in planning and conducting internal audits
  • To identify non-conformities and recommend corrective actions
  • To enhance communication and reporting skills for audit findings
  • To understand the process of continual improvement in laboratory operations

Upon completion of this course, delegates will be equipped with the knowledge and skills to conduct effective internal audits, ensuring their laboratories adhere to ISO/IEC 17025 standards. This proficiency not only contributes to regulatory compliance but also enhances the overall quality and reliability of laboratory testing and calibration processes.

Show moredown

What’s included in this ISO 17025 Internal Auditor Course?

  • ISO 17025 Internal Auditor Examination
  • World-Class Training Sessions from Experienced Instructors 
  • ISO 17025 Internal Auditor Certificate
  • Digital Delegate Pack

Show moredown

ISO 17025 Internal Auditor Exam Information

To achieve the ISO 17025 Internal Auditor, candidates will need to sit for an examination. The exam format is as follows: 

  • Question Type: Multiple Choice  
  • Total Questions: 30 
  • Total Marks: 30 Marks 
  • Pass Mark: 50%, or 15/30 Marks 
  • Duration: 40 Minutes  
  • Open Book/ Closed Book: Closed Book

Show moredown

Not sure which course to choose?

Speak to a training expert for advice if you are unsure of what course is right for you. Give us a call on 01344203999 or Enquire.

ISO 17025 Training FAQs

ISO 17025 is an international standard specifying the competence of testing and calibration laboratories in ensuring accurate and reliable results.
The ISO 17025 Certification Course equips individuals with the skills to implement quality management systems, ensuring compliance and fostering credibility in testing and calibration processes.
ISO 17025 Training is crucial for organisations to meet global standards, enhance testing precision, and promote collaboration between laboratories, ensuring reliable outcomes and maintaining quality.
The duration of an ISO 17025 Course varies but typically ranges from a few days to a couple of weeks, depending on the depth and format of the training program.
The ISO 17025 Training comes with valuable training sessions led by experienced instructors, a digital delegate pack, and a certificate upon completion.
For specific prerequisites for ISO 17025 Training Courses, kindly refer to the respective course pages as they may vary.
Individuals involved in testing and calibration processes, quality management, and laboratory operations can benefit from attending this ISO 17025 Training. This includes Laboratory Managers, Technicians, and Quality Assurance Professionals.
The ISO 17025 Courses cover a range of topics, including understanding ISO 17025 requirements, implementing quality management systems, proficiency in calibration and testing procedures, documentation, and ensuring compliance. Delegates will gain practical insights into maintaining precision and reliability in laboratory practices.
These ISO 17025 Courses have a duration of 1-5 days. For specific information on the duration of the courses, kindly refer to the specific course pages.
ISO 17025 Certifications help delegates develop skills in implementing quality management systems and ensuring precision in testing and calibration processes, enhancing competence in maintaining reliable and accurate results in laboratory operations.
The Knowledge Academy in the United Kingdom is a leading training provider which offers multiple courses, comprehensive course content, experienced instructors, flexible learning options, and industry recognition, making it a reliable choice for attending this course.
Please see our ISO 17025 Training courses available in the United Kingdom
The Knowledge Academy is the Leading global training provider for ISO 17025 Training.
The training fees for ISO 17025 Training in the United Kingdom starts from £2495.
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