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.
A Look at ISO/IEC 17025:2017 - Section 8.9 Management Review Requirements and Utilization
A Look at ISO/IEC 17025 - Section(s) 6.3 & 6.4
Option A and B as Presented in ISO/IEC 17025:2017 along with the Management System Documentation 8.2
A Look at ISO/IEC 17025:2017 - Section 7.9 “Complaints”
ISO/IEC 17025 Section 7.6 - Evaluation of Measurement Uncertainty
Common Findings Detected on Environmental Lab Assessments
A Look at ISO/IEC 17025:2017 - Section 7.7 & Associated Requirements Within PL-1
Improve Your Force Measurements: Tips to Improve Your Force Measurements
A Look at ISO/IEC 17025:2017 - Section 7.8 “Reporting of Results”
The Metals in Cannabis Method with first action status by AOAC & The Road to Get There…
A Look at ISO/IEC 17025:2017 - Section 7.1 “Review of Requests, Tenders, and Contracts”
Common Findings in PJLA Assessments to the ISO/IEC 17025:2017 Standard in 2021
A Look at ISO/IEC 17025:2017 - Section 5.0 “Structural Requirements”
Testing for Gluten and Allergens: Why We Do It and How To Do It Well
A Look at ISO/IEC 17025:2017 - Section 6.6: Externally Provided Products and Services
ASCA Biocompatibility and Basic Safety and Essential Performance FDA Pilot Program with PJLA
ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
A Look at ISO/IEC 17025 2017 - Section 7.10 - Nonconforming Work Section 8.6 - Improvement
5 Steps to the Accreditation Process with Tracy Szerszen
A Look at the Requirements Specified in PJLA Policy on Measurement Uncertainty PL 3
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