As a certified ISO/IEC 17025 auditor, I have seen firsthand how an effective ISO 17025 management review can transform laboratory operations. Laboratories accredited under ISO/IEC 17025:2017 must conduct periodic management reviews to ensure their quality management system (QMS) remains effective, compliant, and aligned with strategic goals. Management reviews are not just a compliance requirement; they…
As a certified ISO/IEC 17025 assessor with over 30 years of experience in Quality Management, I have guided numerous laboratories through successful implementations. Learning how to implement ISO 17025 within your laboratory requires a systematic approach, commitment from management, and a clear understanding of the standard’s requirements. The aim is to develop a quality management…
Understanding and accurately reporting ISO 17025 measurement uncertainty is pivotal for laboratories performing calibrations and tests to maintain compliance with ISO/IEC 17025. This standard outlines the general requirements for competence among testing and calibration laboratories, with a keen emphasis on the consistent presentation of uncertainty data. Laboratories are required to report the uncertainty of measurement…
Achieving ISO/IEC 17025 accreditation is a significant milestone for laboratories, as it not only boosts confidence in their work but is an official recognition of their technical competency and commitment to quality. The accreditation process involves a thorough evaluation by an accreditation body, scrutinizing everything from your laboratory’s quality management system to its day-to-day operations….
Gaining ISO 17025 accreditation is recognized as a significant achievement for laboratories, emphasizing technical competence and a reliable output of results. The benefits of ISO 17025 accreditation are not just a testament to a laboratory’s dedication to quality, but it also reflects a commitment to providing trustworthy data. By achieving ISO 17025 accreditation, your laboratory…
In the world of laboratory testing and calibration, the ISO/IEC 17025:2017 standard serves as a critical benchmark for technical competence. Compliance with this international standard ensures that laboratories are equipped to perform specific types of testing and calibration tasks with precision and reliability. ISO 17025 Equipment requirements are central to this objective. They ensure that…
ISO 17025 Risk management is an essential component of maintaining accreditation for laboratories under ISO/IEC 17025. This international standard specifies the general requirements for the competence to carry out tests and calibrations, including sampling. It breaches the conceptual gap between maintaining high standards and providing a framework through which laboratories can demonstrate consistent operation and…
Corrective action in ISO/IEC 17025 is essential for laboratories to maintain their accreditation and ensure the reliability of their results. When a laboratory identifies nonconformities, whether it’s through internal audits or customer complaints, it must take corrective action. This action is not simply a reactive measure but a structured process that seeks to identify the…
In the scope of ISO 17025 nonconforming work is a critical aspect of laboratory quality management that directly affects the credibility and reliability of test and calibration results. ISO 17025 sets the international standard for testing and calibration laboratories, ensuring that they operate competently and are able to generate valid results. Nonconforming work arises when…
What is ISO 17025 accreditation? It is a prestigious accreditation that signifies a lab’s capability to produce precise & reliable test & calibration results. Issued by authoritative accreditation bodies, this international standard verifies that a lab operates competently and generates valid results, thereby fostering confidence among clients, regulatory authorities, and trade organizations. Laboratories seek ISO/IEC…
