ISO/IEC 17025
How to Prepare for an ISO External Audit (Without Stress)
Introduction External audits under ISO 9001, ISO 14001, ISO 45001, or ISO/IEC 17025 are often seen as stressful events. In reality, stress…
Key Differences Between ISOIEC 17025 and TNI 2016 (What Laboratories Need to Know)
Introduction Many environmental laboratories operate under both ISO/IEC 17025 and TNI 2016. While these standards share a common goal — ensuring laboratory…
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….