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…
Understanding the ISO 9001 Standard begins with recognizing its role as a pivotal international standard that outlines the criteria for an effective quality management system (QMS). Developed and published by the International Organization for Standardization (ISO), ISO 9001:2015 is the most current edition of the standard. This standard is applicable to organizations across various industries…
ISO 9001 Quality Objectives are the bedrock of an organization’s Quality Management System (QMS), serving as measurable targets that drive the enhancement of product and service quality. These objectives are not mere aspirations but quantifiable and actionable goals that reflect an organization’s commitment to customer satisfaction and continuous improvement. Another aspect of quality objectives is…
I’m going to kick things off by demystifying what the ISO 9001:2015 standard is all about and answering the initial question, what is an ISO 9001 quality management system? In its essence, it’s a universally recognized set of guidelines. It doesn’t matter if you’re a start-up or a multinational corporation, these standards are designed to…
I’m going to break down what a Quality Management System (QMS) really means for an organization, and you’re going to find out why it’s much more than a tick-box exercise for compliance. So, what is the purpose of a quality management system? At its core, a QMS is a collection of business processes aimed squarely…
Implementing a Quality Management System (QMS) can be a transformative step for organizations aiming to enhance their efficiency and product quality. With a well-structured QMS, companies can better manage their processes, improve customer satisfaction, and ensure compliance with industry standards. Embarking on a QMS implementation requires a thorough understanding of the company’s objectives and a…
You might be asking yourself, exactly what is a Quality Management System – Definition. Simply put, it’s the backbone of a company’s operations, ensuring that quality isn’t something you just talk about, it’s something you live by every single day. Think of a QMS as the central nervous system of an organization’s drive to deliver…
