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This document provides methods for the testing, calibration and use of volumetric instruments made from glass and plastic in order to obtain the best accuracy in use. NOTE      Testing is the process by which the conformity of the individual volumetric instrument with the appropriate standard is determined, resulting in the determination of its error of measurement at one or more points. This…

This document describes a method for high throughput evaluation of cytotoxic response of 3D model cells exposed to NPs without optical interference. The method in this document is intended to be used in biological testing laboratories that are competent in the culture and growth of cells and the evaluation of cytotoxicity of NPs using 3D-model cells. This method applies to materials that consist…

This document complements and supplements the procedures and general requirements found in ISO/IEC 17025:2017 for laboratories performing evaluations based on the ISO/IEC 15408 series and ISO/IEC 18045.

This document complements and supplements the procedures and general requirements found in ISO/IEC 17025:2017 for laboratories performing testing based on ISO/IEC 19790 and ISO/IEC 24759.

This document complements and supplements the procedures and general requirements found in ISO/IEC 17025:2017 for laboratories performing testing based on ISO/IEC 19790 and ISO/IEC 24759.

This document complements and supplements the procedures and general requirements found in ISO/IEC 17025:2017 for laboratories performing evaluations based on the ISO/IEC 15408 series and ISO/IEC 18045.

This document specifies the neutron reference radiation fields, in the energy range from thermal up to 20 MeV, for calibrating neutron-measuring devices used for radiation protection purposes and for determining their response as a function of neutron energy. This document is concerned only with the methods of producing and characterizing the neutron reference radiation fields. The procedures for…

1 Scope 1.1 General This Standard applies to the reporting of information regarding the conducting of eDNA biological surveys or assessments. This Standard provides a) definitions for terms that are routinely used in the description of eDNA studies; and b) minimum reporting requirements for eDNA studies in a quality assurance/quality control context, including the following: i) survey…

This document specifies requirements and recommendations on the handling, storage, processing and documentation of saliva specimens intended for human DNA examination during the pre-examination phase before a molecular examination is performed. This document is applicable to molecular in vitro diagnostic examination including laboratory developed tests performed by medical laboratories. It can…