ISO/IEC 17025
Control of Data and Information in Laboratories – Beyond Compliance
Introduction Control of data and information is a fundamental requirement of ISO/IEC 17025, TNI 2016, and DoD/DoE QSM. Laboratories rely heavily on…
Method Validation vs Verification: A Practical Guide for Laboratories
Introduction Method validation and verification are essential components of ISO/IEC 17025. They ensure that laboratory methods produce accurate, reliable, and consistent results….
Measurement Traceability in ISO/IEC 17025 – What Auditors Really Look For
Introduction Measurement traceability is a fundamental requirement of ISO/IEC 17025. It ensures that laboratory results are: Accurate Comparable across laboratories Defensible during…
Root Cause Analysis: Why “Human Error” Is Not the Root Cause
Introduction Root cause analysis (RCA) is a critical element of corrective action processes in ISO 9001, ISO 14001, ISO 45001, and ISO/IEC…
Common ISOIEC 17025 Findings in Analytical Laboratories (And How to Avoid Them)
Introduction ISO/IEC 17025 defines the requirements for competence, impartiality, and consistent operation of laboratories. Most laboratories implement systems to meet these requirements….