ISO 17025 Training
ISO 17025 Training
ISO 17025 Internal Auditor
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
Read MoreLess
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
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.
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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.
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
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:Â
- Question Type: Multiple Choice Â
- Total Questions:Â 30Â
- Total Marks:Â 30 MarksÂ
- Pass Mark:Â 50%, or 15/30 MarksÂ
- Duration:Â 40 Minutes Â
- Open Book/ Closed Book:Â Closed Book
ISO 17025 Lead Auditor
Duration
Online Instructor-led (2 days)
Online Self-paced (16 hours)
exam
ISO 17025 Internal 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
Read MoreLess
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 ChecklistsÂ
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
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.
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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.
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
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:Â
- Question Type: Multiple Choice Â
- Total Questions:Â 30Â
- Total Marks:Â 30 MarksÂ
- Pass Mark:Â 50%, or 15/30 MarksÂ
- Duration:Â 40 Minutes Â
- Open Book/ Closed Book:Â Closed Book
ISO 17025 Lead Implementer
Duration
Online Instructor-led (2 days)
Online Self-paced (16 hours)
exam
ISO 17025 Internal Auditor 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
Read MoreLess
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
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 Course.
Read MoreLess
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.
What’s included in this ISO 17025 Lead Implementer Course?
- ISO 17025 Lead Implementer Examination
- World-Class Training Sessions from Experienced InstructorsÂ
- ISO 17025 Lead Implementer Certificate
- Digital Delegate Pack
ISO 17025Â 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:Â
- Question Type: Multiple Choice Â
- Total Questions: 30Â
- Total Marks: 30 MarksÂ
- Pass Mark: 50%, or 15/30 MarksÂ
- Duration: 40 Minutes Â
- Open Book/ Closed Book:Â Closed Book
ISO 17025 Foundation
Duration
Online Instructor-led (2 days)
Online Self-paced (16 hours)
exam
ISO 17025 Internal Auditor Exam
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
Read MoreLess
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
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.
Read MoreLess
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 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.
What’s included in this ISO 17025 Foundation Course?
- World-Class Training Sessions from Experienced Instructors
- ISO 17025 Foundation Certificate
- Digital Delegate Pack
ISO 17025 Foundation Exam InformationÂ
To achieve the ISO 17025 Foundation, candidates will need to sit for an examination. The exam format is as follows:Â
- Question Type: Multiple Choice Â
- Total Questions:Â 30Â
- Total Marks:Â 30 MarksÂ
- Pass Mark:Â 50%, or 15/30 MarksÂ
- Duration:Â 40 Minutes Â
- Open Book/ Closed Book:Â Closed Book
Maximize Your Investment with ISO/IEC 17025 Testing & Calibration Laboratories Training Bundles
Our training experts have curated a comprehensive range of ISO/IEC 17025 Testing and Calibration Laboratories course bundles designed to strengthen your professional competence and enhance laboratory reliability, technical accuracy, and compliance with accreditation requirements.
PHYSICAL CLASSES
- Instructor-led ISO/IEC 17025 training
- Clause-by-clause requirements
- Laboratory audit case workshops
- Accreditation readiness support
Online Classes
- Live virtual lab audit sessions
- Interactive compliance discussions
- Digital learning materials
- Certification guidance support
Enterprise Solutions
Contact For Price
- Organization-wide lab programs
- Customized ISO/IEC 17025 training
- Progress tracking & reporting
- Cost-effective enterprise solutions
E-LEARNING
- Self-paced ISO/IEC 17025 learning
- Full course access
- Practical audit exercises
- Certificate upon completion
PHYSICAL CLASSES
- Instructor-led ISO/IEC 17025 training
- Clause-by-clause requirements
- Laboratory audit case workshops
- Accreditation readiness support
Online Classes
- Live virtual lab audit sessions
- Interactive compliance discussions
- Digital learning materials
- Certification guidance support
E-learning
- Self-paced ISO/IEC 17025 learning
- Full course access
- Practical audit exercises
- Certificate upon completion
Enterprise Solutions
Contact For Price
- Organization-wide lab programs
- Customized ISO/IEC 17025 training
- Progress tracking & reporting
- Cost-effective enterprise solutions
Not Sure Which Course is Right for You?
Speak to a training expert for advice if you are unsure of what course is right for you. Give us a call onÂ
Why Choose BGMC ISO/IEC 17025 Testing & Calibration Laboratories – Refresher Training
Globally Recognized:
BGMC’s ISO/IEC 17025 Refresher Training aligns with internationally accepted laboratory competence and accreditation standards, ensuring your knowledge remains current and compliant with global testing and calibration requirements.
Comprehensive Learning:
Covers the latest updates to ISO/IEC 17025:2017, including laboratory management requirements, technical competence, method validation, measurement uncertainty, traceability, equipment control, risk-based thinking, and continual improvement.
Career Boost:
Enhance your professional credibility in laboratory quality and technical management with refreshed certification, supporting your role as a laboratory auditor, quality manager, technical manager, or laboratory professional.
Hands-On Application:
Apply real-world laboratory practices through updated case studies, method validation exercises, measurement uncertainty calculations, internal audit simulations, nonconformity handling, and corrective action scenarios.
Progression Path:
A strong foundation for advancing into specialized roles such as ISO/IEC 17025 Lead Auditor, Lead Implementer, Laboratory Quality Manager, Technical Manager, or Integrated Management System (IMS) Expert.
ISO 17025 Training FAQs
What is ISO 17025?
ISO 17025 is an international standard that specifies the requirements for the competence of testing and calibration laboratories. It ensures that laboratories produce valid and reliable results through effective quality management systems and technical proficiency.
What are the 5 requirements of ISO 17025?
ISO 17025 requires management and technical competence, quality assurance, personnel qualifications, and suitable equipment and facilities. It ensures reliable testing and calibration through a robust quality management system, skilled staff, and appropriate resources for consistent and valid results.
What is the principle of ISO 17025?
The principle of ISO 17025 is to ensure that laboratories are technically competent and produce valid, reliable results. It focuses on establishing a quality management system, maintaining appropriate resources, and ensuring consistent, accurate testing and calibration practices to meet international standards.
Do you need ISO 17025 if you have ISO 9001?
While ISO 9001 focuses on overall quality management systems, ISO 17025 is specifically for testing and calibration laboratories. If your organisation requires accredited testing or calibration services, ISO 17025 is necessary, even if you already hold ISO 9001 certification.
What is the difference between ISO 17025 and GMP?
ISO 17025 is focused on the competence of testing and calibration laboratories, ensuring accurate and reliable results. GMP (Good Manufacturing Practice) ensures the quality, safety, and efficacy of products during manufacturing. While ISO 17025 targets laboratories, GMP applies to production environments.
What skills can be developed through ISO 17025 Certifications?
ISO 17025 certification helps develop skills in quality management, laboratory operations, testing and calibration methods, risk management, and compliance with international standards. It also enhances expertise in ensuring reliable, accurate results and maintaining effective management systems in laboratories.
Can ISO 17025 Certification improve my company's operational efficiency?
Yes, ISO 17025 certification can improve your company’s operational efficiency by standardising processes, ensuring accurate and reliable results, enhancing quality control, reducing errors, and optimising resource management. This leads to improved productivity, reduced costs, and increased customer satisfaction.
What industries require ISO 17025 Certification?
Industries that require ISO 17025 certification include testing and calibration laboratories, pharmaceuticals, environmental testing, food safety, automotive, manufacturing, electronics, and healthcare. It ensures compliance with industry standards and guarantees accurate, reliable testing and calibration results across various sectors.
Can ISO 17025 Certification help in global business expansion?
Yes, ISO 17025 certification can support global business expansion by enhancing credibility, demonstrating compliance with international standards, and ensuring reliable testing and calibration services. It fosters trust with global clients, opens opportunities in regulated markets, and improves competitiveness worldwide.
What does this ISO 17025 Certification aim to achieve?
ISO 17025 certification aims to ensure the competence of testing and calibration laboratories, guaranteeing accurate, reliable results, and compliance with international standards. It also enhances operational efficiency, quality control, and consistency in laboratory processes.
What are the benefits of ISO 17025 Training?
ISO 17025 training provides benefits such as enhanced understanding of quality management systems, improved laboratory practices, increased compliance with international standards, better risk management, and the ability to ensure accurate, reliable testing and calibration results, boosting operational efficiency.
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