IT Security and Privacy — A framework for identity management — Part 2: Reference architecture and r...
This document:
— provides guidelines for the implementation of systems for the management of identity information, and
—specifies requirements for the implementation and operation of a framework for identity management.
This document is applicable to any information system where information relating to identity is processed or stored.
Matériel d’anesthésie et de réanimation respiratoire — Exigences générales pour canules et équipemen...
ISO 18190:2016 spécifie les exigences générales communes aux canules et équipement connexe et applicables aux normes spécifiques de dispositifs qui y font référence.
Les exigences d'une norme spécifique d'un dispositif prévalent sur l'ISO 18190:2016.
NOTE Les exigences générales contenues dans l'ISO 18190:2016 ont historiquement été référencées dans plus de deux…
Surface chemical analysis — Total reflection X-ray fluorescence analysis of water
ISO 20289:2018 provides a chemical method for technicians working with Total Reflection X-ray Fluorescence (TXRF) instrumentation to perform measurements of water samples, according to good practices, with a defined degree of accuracy and precision. Target users are identified among laboratories performing routine analysis of large numbers of samples, which also comply with ISO/IEC 17025.
ISO…
Petroleum products — Determination of the filterability of lubricating oils — Part 2: Procedure for ...
ISO 13357-2:2017 specifies a procedure for the evaluation of the filterability of dry lubricating oils, particularly those designed for hydraulic applications. The procedure only applies to mineral-based oils, since fluids manufactured from other materials (e.g. fire-resistant fluids) might not be compatible with the specified test membranes. The range of application has been evaluated with oils…
Health informatics — International patient summary
This document defines the core data set for a patient summary document that supports continuity of care for a person and coordination of their healthcare. It is specifically aimed at supporting the use case’ scenario for ‘unplanned, cross border care’ and is intended to be an international patient summary (IPS). Whilst the data set is minimal and non-exhaustive, it provides a robust, well-defined…
Information technology — Information modelling for VR/AR/MR based learning, education and training s...
This document describes guidelines for developing education and training systems using VR/AR/MR technology. It defines VR/AR/MR based information modelling that can be used for education and training systems. It provides procedures and methods to be used when developing 3D VR/AR/MR based education and training systems using ISO/IEC JTC 1 standards. It also provides a systematic approach to…
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for circul...
This document gives guidelines on the handling, storage, processing and documentation of human venous whole blood specimens intended for the examination of RNA isolated from circulating tumour cells (CTCs) during the pre-examination phase before a molecular examination is performed.
This document is applicable to molecular in vitro diagnostic examinations performed and/or developed by medical…
