How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017

How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 is a webinar that covers topics such as:

  • What are the new requirements of ISO/IEC 17015:2017?
  • Have the rules changed? Recall the differences between ISO/IEC 172025:2005 and the newly revised version, 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?
  • Identify the new documents and records required by the standard
  • Defining a QMS
  • Implement a quality documentation transition plan to ensure compliance with the newly revised standard
  • New and revised Quality Management Requirements
  • Management Components of a QMS
  • New and revised Technical Requirements
  • Technical Components of a QMS
  • Ensuring analytical competency
  • Method Selection, Validation and Verification
  • Identifying adjustments to your existing ISO/IEC 17025:2005 Quality Documentation

How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 is intended for:

  • QA Managers
  • Laboratory Managers
  • Laboratories accredited to ISO/IEC 17025:2005
  • QC Analysts
  • Laboratories seeking to become accredited to ISO/IEC 17025

Future Events

How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

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