ISO 17025 Training - Vietnam

ISO 17025 Training

ISO 17025 is an international standard that outlines the requirements for the competence of testing and calibration laboratories. Our ISO 17025 Training provides essential knowledge to implement and maintain Quality Management Systems compliant with the standard.

REASONS TO CHOOSE

Learn about the global lab standards for precision and reliability
Gain in-depth knowledge about quality assurance
Acquire proficiency in implementing quality control measures
Enhance your skills for ensuring data reliability and accuracy
Ensure compliance with ISO norms with our ISO 17025 Training Courses

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ISO 17025 Training

Duration

Online Instructor-led (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

More information

See dates & prices

Who should attend this ISO 17025 Foundation Course?

The ISO 17025 Foundation Training 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 Training Course.

ISO 17025 Foundation 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.

More information

See dates & prices

What’s included in this ISO 17025 Foundation Course?

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

More information

See dates & prices

More information

See dates & prices

Duration

Online Instructor-led (2 days)

Online Self-paced (16 hours)

exam

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

More information

See dates & prices

Who should attend this ISO 17025 Internal Auditor Training Course?

The ISO 17025 Internal Auditor Training Course is designed to give delegates a foundational understanding of the ISO 17025 standard, used to audit testing and calibration laboratories. This course is benefiting 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 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 Course Overview

The ISO 17025 Internal Auditor Course is designed to equip participants with the essential skills to perform laboratory internal audits, ensuring adherence to the ISO/IEC 17025 standard. This standard specifies the general requirements for the competence of testing and calibration laboratories, highlighting the critical role of quality management systems in these environments.

Professionals who are Laboratory Managers, Quality Managers, or responsible for ensuring compliance with ISO/IEC 17025 should aim to learn this subject. A thorough understanding of internal auditing is crucial for upholding the integrity and reliability of laboratory testing and calibration processes.

The Knowledge Academy's 2-day training equips delegates with the essential knowledge and practical skills to conduct effective internal audits in accordance with ISO/IEC 17025. This course delves into critical concepts, audit methodologies, and best practices, enabling delegates to significantly enhance 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 completing this course, delegates will gain the knowledge and skills to perform effective internal audits and ensure their laboratories meet ISO/IEC 17025 standards. This expertise ensures regulatory compliance and improves the quality and reliability of laboratory testing and calibration processes.

More information

See dates & prices

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

More information

See dates & prices

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

More information

See dates & prices

Duration

Online Instructor-led (5 days)

Online Self-paced (40 hours)

exam

ISO 17025 Lead Auditor Exam

ISO 17025 Lead Auditor Course Outline

Module 1: Introduction to ISO 17025

ISO
ISO 17025

Module 2: Requirements of ISO 17025

Overview
Requirements of ISO 17025

Module 3: Relationship between ISO 19011 and ISO 17025

ISO 19011
Relationship between ISO 19011 and ISO 17025

Module 4: Scope

Overview
Scope of ISO 17025

Module 5: Normative References

Introduction to Normative References

Module 6: Terms and Definitions

Overview
Terms and Definitions

Module 7: General Requirements

Overview
Impartiality
Confidentiality

Module 8: Structural Requirements

Overview of Structural Requirements

Module 9: Resource Requirements

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
Ensuring Result Validity
Reporting of Results
Complaints
Nonconforming Work
Control of Data and Information Management

Module 11: Management System Requirements

Options
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

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, APLAC

Description of ILAC
ILAC’s Global Role
Abbreviations
ILAC Documents
ILAC P10 Traceability Policy

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

Case studies on clauses 7 and 8

Module 26: Guidelines for Auditing: ISO 19011

ISO 19011 Auditing Guidelines

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

GUM (Uncertainty)
PT/ILC
Traceability

Module 28: Opening and Closing Meeting Activities

Opening Meeting
Closing Meeting

Module 29: Auditing Technical Methods

Overview

Module 30: Reporting Audit Results

Internal Audit Report

Module 31: Audit Checklists and Audit Reports

ISO 17025:2017 Audit Checklist for Laboratory Accreditation System Requirements
Content of ISO/IEC 17025:2017 Audit Checklists

Module 32: Review of Standards and Internal Auditing Issues

Review of Standards
Internal Auditing Issues

Module 33: Introduction to Lab Management System

Standards and Regulatory Frameworks
Laboratory Management Systems
Laboratories and Accreditation Fundamental Principles
Testing and Calibration Concepts

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

More information

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Who should attend this ISO 17025 Lead Auditor Course?

The ISO 17025 Lead Auditor Training Course equips professionals with the expertise to lead and perform audits of testing and calibration laboratories, ensuring compliance with ISO 17025 standards. This training is profitable for various 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 Course

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

ISO 17025 Lead Auditor Course Overview

ISO 17025 Lead Auditor Training is designed to maintain international standards in testing and calibration laboratories. The ISO 17025 standard ensures these laboratories consistently deliver high-quality, competent, and reliable results. With growing demands for precise and accurate data in industries like healthcare, environmental monitoring, and manufacturing, compliance with ISO 17025 is essential.

Enhancing and ensuring the quality of laboratory processes is essential for professionals aiming to learn ISO 17025. Roles such as Quality Managers, Laboratory Supervisors, and Lead Auditors are crucial to maintaining standards and compliance. This ISO 17025 Training equips them to conduct effective audits, pinpointing areas for improvement, non-conformities, and potential risks.

The Knowledge Academy offers a comprehensive 5-day ISO 17025 Training Course designed to equip delegates with essential skills for leading ISO 17025 audits. This course covers critical concepts and audit techniques, providing a thorough understanding of the standard. Delegates will gain the knowledge needed to contribute significantly to laboratory quality assurance. This course will be conducted under the guidance of 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

After completing this course, delegates will gain the expertise to lead ISO 17025 audits, ensuring compliance with international standards. This course will enhance the quality and reliability of laboratory testing and calibration processes. Knowledge of these skills will open doors for career advancement and contribute to organisational excellence.

More information

See dates & prices

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

More information

See dates & prices

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

More information

See dates & prices

Duration

Online Instructor-led (3 days)

Online Self-paced (24 hours)

exam

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

More information

See dates & prices

Who should attend this ISO 17025 Lead Implementer Course?

The ISO 17025 Lead Implementer Training 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 Course

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

ISO 17025 Lead Implementer 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.

More information

See dates & prices

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

More information

See dates & prices

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

More information

See dates & prices

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 +44 1344 203999 or Enquire.

ISO 17025 Training FAQs

What is ISO 17025?

ISO 17025 is an international standard specifying the competence of testing and calibration laboratories in ensuring accurate and reliable results.

What are the benefits of taking ISO 17025 Certification Courses?

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.

How long does it take to study an ISO 17025 Training Course?

The duration of our ISO 17025 Training Course depends on the course you select. Please visit the course page of the desired course you wish to pursue.

What does an ISO 17025 Course include?

The ISO 17025 Training comes with valuable training sessions led by experienced instructors, a digital delegate pack, and a certificate upon completion.

Are there any prerequisites of taking this ISO 17025 Training?

For specific prerequisites for ISO 17025 Training Courses, kindly refer to the respective course pages as they may vary.

Who should attend this ISO 17025 Training?

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.

What skills can be developed through ISO 17025 Certifications?

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.

What does the ISO 17025 Certification exam include?

The ISO 17025 Certification exam includes assessments on laboratory management, quality control, and technical requirements for testing and calibration laboratories.

How can ISO 17025 Course benefit my career?

ISO 17025 Course enhances your skills in laboratory management and quality assurance, increasing job opportunities and career advancement.

What types of jobs can I get with an ISO 17025 Certification?

Jobs include Quality Manager, Laboratory Manager, Calibration Technician, and roles in compliance and quality assurance.

Can the ISO 17025 Courses help me transition to a new field?

Yes, ISO 17025 Course provides transferable skills in quality management, aiding transitions to sectors like pharmaceuticals, manufacturing, and environmental testing.

Can ISO 17025 Certification improve my company's operational efficiency?

Yes, ISO 17025 Certification improves operational efficiency by ensuring accurate testing, reliable results, and adherence to international standards.

What industries require ISO 17025 Certification?

Industries requiring ISO 17025 Certification include pharmaceuticals, manufacturing, environmental testing, food and beverage, and aerospace.

Can ISO 17025 Certification help in global business expansion?

Yes, ISO 17025 Certification helps in global business expansion by ensuring international recognition and compliance with global quality standards.

Why choose The Knowledge Academy in Vietnam over others?

The Knowledge Academy stands out as a prestigious training provider known for its extensive course offerings, expert instructors, adaptable learning formats, and industry recognition. It's a dependable option for those seeking ISO 17025 Certification.

What are the best ISO 17025 Training courses in Vietnam?

Please see our ISO 17025 Training courses available in Vietnam

Which is the best training institute/provider of ISO 17025 Training in Vietnam?

The Knowledge Academy is the Leading global training provider for ISO 17025 Training.

What is the cost/training fees for ISO 17025 Training in Vietnam

The training fees for ISO 17025 Training in Vietnam starts from $3195

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Many delivery methods

Flexible delivery methods are available depending on your learning style.

High quality resources

Resources are included for a comprehensive learning experience.

"Really good course and well organised. Trainer was great with a sense of humour - his experience allowed a free flowing course, structured to help you gain as much information & relevant experience whilst helping prepare you for the exam"

Joshua Davies, Thames Water