Automation systems and integration — Key performance indicators (KPIs) for manufacturing operations ...
ISO 22400 defines key performance indicators (KPIs) used in manufacturing operations management.
ISO 22400-2:2014 specifies a selected number of KPIs in current practice. The KPIs are presented by means of their formula and corresponding elements, their time behaviour, their unit/dimension and other characteristics. ISO 22400-2:2014 also indicates the user group where the KPIs are used, and the…
Document management — 3D use of Product Representation Compact (PRC) format — Part 1: PRC 10001
ISO 14739-1:2014 describes PRC 10001 of a product representation compact (PRC) file format for three dimensional (3D) content data. This format is designed to be included in PDF (ISO 32000) and other similar document formats for the purpose of 3D visualization and exchange. It can be used for creating, viewing, and distributing 3D data in document exchange workflows. It is optimized to store,…
Information technology — Common Biometric Exchange Formats Framework — Part 4: Security block format...
ISO/IEC 19785-4:2010 specifies security block formats (see ISO/IEC 19785-1) registered in accordance with ISO/IEC 19785-2 as formats defined by the CBEFF biometric organization ISO/IEC JTC 1/SC 37, and specifies their registered security block format identifiers. [The security block format identifier is recorded in the standard biometric header (SBH) of a patron format (or defined by that patron…
ISO 15238:2016 specifies a procedure for the determination of the total cadmium content of coal.
This procedure has not been validated with coals that spontaneously ignite. Prior to use with such sample types, users should validate the method.
Clinical investigation of medical devices for human subjects — Good clinical practice
This document addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the clinical performance or effectiveness and safety of medical devices.
For post-market clinical investigations, the principles set forth in this document are intended to be followed as far as relevant, considering the nature of the…
Information technology — User interface component accessibility — Part 20: Developing audiovisual co...
This document provides requirements and recommendations on the development of accessible audiovisual content.
It requires and recommends a variety of different accessibility components, dealt with in further detail in additional parts of the ISO 20071 series, that meet different user accessibility needs. It also provides guidance related to translations, localizations, timing, importance, and…
Condition monitoring and diagnostics of machines — Data interpretation and diagnostics techniques — ...
This part of ISO 13379 gives guidelines for the data interpretation and diagnostics of machines. It is intended to
— allow the users and manufacturers of condition monitoring and diagnostics systems to share common
concepts in the fields of machine diagnostics;
— enable users to prepare the necessary technical characteristics that are used for the further diagnosis of
the condition of the machine…
Presentation of Lexicographic Entries in General Language Dictionaries – Fundamentals and Recommenda...
This international standard focuses on the presentation of lexicographic articles in language dictionaries, either monolingual, bilingual or multilingual, following a lexicographic lemma-oriented approach, being addressed for human end-users. Concerning the modelling of the underlying data, the ISO 1951:2007 follows the ISO 24613 series.
The document provides recommendations to deal with the…
Cybersecurity — IoT security and privacy — Cybersecurity labelling framework for consumer IoT
This document defines a Universal Cybersecurity Labelling Framework for the development and implementation of cybersecurity labelling programmes for consumer IoT products and includes guidance on the following topics:
• Risks and threats associated with consumer IoT products;
• Stakeholders, roles and responsibilities;
• Relevant standards and guidance documents;
• Conformity assessment options…
Acoustics — Noise control design procedures for open plant
This International Standard defines the procedures for noise control of mainly open plants.
It is applicable to the following:
_ specification of procedures for noise control during engineering of a new plant and modification/extension of
existing plants (construction noise procedures are outside the scope of this International Standard but should
be considered);
_ definition of responsibilities…