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ISO/IEC 17025 And ISO/IEC 17020, Which Is The "Right" Standard for You? 2021

Developing a QMS is a prerequisite for getting accredited. ISO/IEC 17020 sets out general criteria for the operation of various types of bodies performing inspection. ISO/IEC 17025 is the international standard for the General requirements for the competence of testing and calibration laboratories. Which is the right standard for you?

Why Should You Attend:

This webinar will discuss the changes in the standard and their impact on your QMS. It will provide you with an overview of the salient differences and similarities between the old and the new versions of ISO/IEC 12025 standard and ISO/IEC 17020.

ISO/IEC 17020 sets out general criteria for the operation of various types of bodies performing inspection. ISO/IEC 17025 is the international standard specifically focused on the requirements for the competence of testing and calibration laboratories A new version was released on November 19, 2017. What are the changes and how will they impact your current Quality Management System? What are the new requirements of ISO/IEC 17025:2017? How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?

Areas Covered in the Webinar:

Upon completion of this session, attendees will learn:

  • What is ISO/IEC 17020
  • What is ISO/IEC 17025
  • How does ISO/IEC 17025 differ from ISO/IEC 17020
  • What are the most significant changes in the latest version of ISO/IEC 17025?
  • What must my lab do to comply?

Who Will Benefit:

This webinar will provide valuable assistance to:

  • Managers Laboratory.
  • QA Managers,
  • QC Analysts

Contact Organizer

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(1+) 206-575-7771
World Medical Events Company
12922 SE 299th Street, Auburn WA 98092 USA