This webinar will look at Section 8.7 of ISO/IEC 17025:2017 in regards to corrective action. This will look at the requirements which will include question an organization should ask itself when a nonconformance has occurred and corrective action is needed. The differences between correction vs corrective action will be explored. Cause analysis will be brought to light and how an effective cause analysis can greatly reduce the chances of a nonconformance repeating itself.
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
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
Requirements for Internal Audits in ISO/IEC 17025:2017
Streamlining Laboratory Efficiency with Greg Cenker
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