Reference Material Producers Requirements and Procedures
ISO/IEC 17000 defines accreditation as “third-party attestation (5.2) related to a conformity assessment body (2.5) conveying formal demonstration of its competence to carry out specific conformity...
The ISO Committee on Reference Materials (ISO/REMCO) published the first and second editions of this Guide in 1981 and 2000, respectively. Since the second edition was published, there has been...
The production of reference materials (RMs) is a key activity for the improvement and maintenance of a worldwide coherent measurement system. As detailed in ISO Guide 33[1], RMs with different...
Reference Materials (RMs) are used in all stages of the measurement process, for method validation, calibration and quality control. They are used for assessing laboratory proficiency through...
Reference materials (RMs) are used in all stages of the measurement process, including for method validation, calibration, and quality control. They are also used in interlaboratory comparisons for...
Reference materials (RMs) and certified reference materials (CRMs) (defined in 2.1 and 2.2) are widely used for the calibration of measuring apparatus, for the evaluation of measurement procedures...
This International Standard, based upon ISO/IEC 17025 and ISO 9001, specifies requirements for competence and quality that are particular to medical laboratories1. It is acknowledged that a country...
ISO/IEC 17025:2017 - General requirements for the competence of testing and calibration laboratories
This document has been developed with the objective of promoting confidence in the operation of laboratories. This document contains requirements for laboratories to enable them to demonstrate they...