Preparing for an ISO/IEC 17025:2017 Accreditation Assessment

One of the key factors to successfully achieving accreditation is to be prepared for an assessment. Understand your obligations with your accreditation body Application documents and preliminary document review content and timelines Assessment Witnessing Expectations Corrective Action Timelines Notifications of Significant Changes Impacting Accreditation Understand what you are being assessed to i.e. ISO/IEC 17025:2017 Training on the ISO/IEC 17025:2017 standard Quality Management System (QMS) in relation to ISO/IEC 17025:2017, QMS documents; SOP Requirements, Working Instructions Proficiency Testing and why it is important Measurement Uncertainty; is it necessary and how does it apply This webinar will discuss the accreditation process, the expectation of the laboratories becoming & maintaining accreditation and an overview of the key technical areas of the ISO/IEC 17025 standard, and our most common top 5 findings during an assessment.

A Look at ISO/IEC 17025:2017 - Review of Section 8.5 “Actions to Address Risks and Opportunities”
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A Look at ISO/IEC 17025:2017 - Review of Section 8.5 “Actions to Address Risks and Opportunities”

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Workshop Series - Overview of ISO/IEC 17025:2017 Requirements for Laboratory Accreditation

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