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
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
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
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