Online ISO/IEC 17025:2017 Foundation Training

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  • Course Area:


  • Continuing Education Units (CEUs):


  • Course Duration:

    8 Hours

  • Accreditation:

    CQI and IRCA approved training partner
  • Format:

    Virtual Learning Course

Finally, an industry-leading online & blended training solution for ISO Standards, Quality Auditing & Medical Device Training!

Comply Guru LLC, based in Chicago, IL, offers a growing portfolio online & blended training courses on various ISO Standards, Quality Auditing and Medical Device Regulations to enable its Learners to get the knowledge and skills they need from home, work or anywhere!

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This Online ISO/IEC 17025:2017 Foundation Course (via Virtual Learning) is ideal for anyone that wants to gain a comprehensive understanding of the requirements of ISO/IEC 17025:2017.

Course Certification

This course is certified by Comply Guru™. Successful completion will entitle each Learner to receive a digital Certificate of Completion.

Assessment Methodology

In order to successfully complete this course, each Learner will need:

  • 100% attendance of the virtual delivery
  • Module 1: Introduction to ISO/IEC 17025:2017

    In this module, an overview of the standard will be provided including coverage of the structure, scope, purpose and benefits of ISO/IEC 17025:2017. We will also explore some of the key concepts that underpin the standard including: Relationship to ISO 9001:2015, PDCA Cycle, Process Approach and Risk Based Thinking.

  • Module 2: General and Structural Requirements

    In this module, we will explore the requirements for ensuring that the laboratory performs its work in an impartial and confidential manner. We will also explore the requirements for establishing and defining the laboratories organization and management structure.

  • Module 3: Resource Requirements

    In this module, we will explore the requirements for ensuring that the personnel, facilities, equipment, systems and support services that are required by the laboratory to perform its activities are available.

  • Module 4: Process Requirements – Pre-Testing and Testing

    In this module, we will explore the requirements for reviewing requests, tenders and contracts, method selection, sampling, technical records and considerations for handling of test or calibration items on receipt at the laboratory.

  • Module 5: Process Requirements – Post Testing

    In this module, we will explore how the laboratory ensures the validity of its results and the specific requirements related to reporting of results. The requirements for managing customer complaints and handling of non-conforming work will also be explored.

  • Module 6: Management System Requirements

    In this module, we will explore the requirements related to the laboratories management system including the specific requirements for managing documentation, addressing risks and opportunities, conducting internal audits and management reviews, implementing corrective actions and demonstrating improvement.

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