This webinar will review the requirements specified in ISO/IEC 17025:2017 for internal audits. We will explore how to maximize the benefit from these requirements to assure compliance with the ISO/IEC 17025:2017, and compliance with your own quality management system is being maintained. The importance of reviewing objective evidence will be highlighted. Ideally if there is a nonconformance issue relating ISO/IEC 17025:2017 or your own quality management system, your internal audit program will identify it. Presented By: Michael Kramer, PJLA Calibration Program Manager and Lead Assessor
Measurement Uncertainty and Decision Rules with Dr. Susan Audino
Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2023
Adding DOECAP-AP Accreditation to a DoD ELAP Accredited Laboratory
A Look at ISO/IEC 17025:2017 - Section 6.6 - Externally Provided Products and Services
Understanding the PJLA Flexible Scope Policy for Testing Labs, RMPS, and PTPs
A Look at ISO/IEC 17025:2017 - Overview of the Requirements Specified for Equipment in Section 6.4
Measurements Gone Wrong Webinar with PJLA & Henry Zumbrun
A Look at ISO/IEC 17025:2017 - Requirements for Corrective Action
An Overview of 17043 Proficiency Testing Provider Accreditation with PJLA
A Review of the Revised PJLA Policy PL-4 “Scopes of Accreditation”
Understanding the Types of Reference Materials, Their Differences, and Their Uses
I Submitted a Complaint - Why is this Organization Still Accredited?
Use of Accreditation Symbols and References to Accreditation
A look at ISO/IEC 17025:2017 - Section 7.2 “Selection, Verification, and Validation of Methods”
A Look at ISO/IEC 17025:2017 - Review of Section 8.5 “Actions to Address Risks and Opportunities”
A Look at ISO/IEC 17025:2017 - Section 7.6 “Evaluation of Measurement Uncertainty” for Testing Labs
Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2022
Top FDA Warning Letters Related to Calibration with Walter Nowocin
Streamlining Laboratory Efficiency with Greg Cenker
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