Laboratories are required to have a program of internal audits to assess whether their operations comply with ISO/IEC 17025 requirements on an ongoing basis. This involves auditing both management and technical activities to identify gaps, and to drive improvements. A positive audit culture is essential to ensure that internal technical …
Read More ...A corrective action is a mandatory activity for all laboratories accredited to ISO/IEC 17025. It should, however, not be seen as a “rule” or a singular step, but as a core process of an interrelated, functional Quality Management System. Laboratories often struggle with nonconformances and corrective actions, where they are …
Read More ...If your testing or calibration laboratory is looking to achieve accreditation to ISO/IEC 17025:2017, you may be unclear as to how to practically address the requirement of impartiality and how much effort to go to. This article will assist with this, by providing an overview of what is required by …
Read More ...With the introduction of the 2017 revision of ISO/IEC 17025, which seeks greater alignment with ISO 9001, laboratories now need to implement risk-based thinking in relation to their activities. This was addressed in previous versions of the standards using preventive action, but the introduction of risk-based thinking requires the laboratory …
Read More ...In late 2017, the third edition of the ISO/IEC 17025 standard was published. This is the latest revision of the standard on which testing and calibration laboratories base their Quality Management Systems. Some of the changes to the older 2005 version, such as the new structure and the less prescriptive …
Read More ...Testing is used in many industries, but offering testing as a professional service requires that any type of measurement, sampling or calibration laboratory pass through the process of accreditation. When it comes to the accreditation, the company is obligated to show conformity to the ISO 17025 standard. Compliance with the …
Read More ...The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required …
Read More ...A while back, I was faced with a challenge when the CEO of my company asked me to present to management how I would be improving our company’s ISO 17025 system, according to the revised version, ISO 17025:2017. As I was quite new to the management team, I had to …
Read More ...If your organization is seeking to adopt ISO 17025 in your laboratory environment, the looming question(s) are likely some of the following: How do we get there? What do we need to do? Are we prepared? What steps should be taken? How much money will this cost us? How long will …
Read More ...How can ISO 17025 help improve laboratory measurements? Present industry research and development depends heavily on precise measuring. To be able to meet that requirement, modern laboratories must use high-quality measuring equipment. Also, to obtain the correct measurement result, the laboratory must employ an organized approach in the measurement process. …
Read More ...If you noticed the release of the 2017 update of ISO 17025:2017, you might wonder what this standard is all about, and how it relates to ISO 9001:2015 and the Quality Management System (QMS) in your organization. You might well ask: What is ISO 17025:2017, and how is it similar and …
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