1030V: Overview of ISO/IEC 17025:2017 - VIRTUAL - May 1-2, 2024

1030V: Overview of ISO/IEC 17025:2017 - VIRTUAL - May 1-2, 2024

  • $600.00


Date: May 1-2, 2024

Time: 11:30 am to 3:30 pm ET each day

Member price: $510.00
Non-member price: $600.00

This course provides a general overview of the ISO/IEC 17025 standard. It provides a high-level look at the requirements of the standard and how those requirements drive the design of laboratory quality systems. 



Participants require access to a computer and a microphone in order to take this training. A headset with microphone is highly recommended. A webcam is recommended, but not required. 

This is a virtual course.

Please note: Only 1 participant per registration.

Contact training@cala.ca (613-233-5300) for group training options.

 

Who should attend

This is an overview for the members of a laboratory who need an understanding of the requirements of the standard, including laboratory staff who:

  • Conduct testing or calibration
  • Support laboratory activities

Laboratory staff involved with interpreting the standard, auditing, writing processes and procedures, or maintaining the management system should enroll in 1010: Understanding ISO/IEC 17025:2017.

Course overview

This one-day course looks at the ISO/IEC 17025 standard and the relationship between a laboratory’s quality system and the standard. It explains the reasons for aspects of the quality system such as document control, traceability of trace results, dealing with non-conformances, and internal audits. 

 

Objectives

After completing this course, participants will be able to:

  • Describe the basic management system requirements in ISO/IEC 17025
  • Describe how a laboratory demonstrates that the equipment used and method selected for testing are fit for purpose
  • Explain the purpose of document control
  • Describe the actions laboratories can take to continually improve their conformance to ISO/IEC 17025
  • Describe how laboratories demonstrate that testing methods are fit for purpose
  • Describe the requirements for quality control