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This document provides requirements, specifications and guidance for an architecture of a supplier-neutral industrial digital ecosystem. It includes a standardized connectivity and services architecture, and a standardized use case architecture with methods to specify atomically re-usable scenarios and events, which can be used to specify the characteristics of standardized industry use cases.…

This document specifies the International Standard identifier for libraries and related organizations (ISIL), which comprises a set of standard identifiers used for the unique identification of libraries and related organizations such as museums and archives with a minimum impact on already existing systems. An ISIL identifies an organization, i.e. a library or a related organization, or one of…

This document defines good study practice for the planning, design, conduct, recording and reporting of clinical performance studies carried out to assess the clinical performance and safety of in vitro diagnostic (IVD) medical devices for regulatory purposes. NOTE 1 The purpose of these studies is to assess the ability of an IVD medical device in the hands of the intended user, to yield…

This document describes the methods for determining the activity in becquerel (Bq) of gamma‑ray emitting radionuclides in test samples by gamma-ray spectrometry. The measurements are carried out in a testing laboratory following proper sample preparation. The test samples can be solid, liquid or gaseous. Applications include: — routine surveillance of radioactivity released from nuclear…

This document gives the safety requirements and measures for stationary and displaceable — surface planing machines, also called jointers, — thickness planing machines, also called planers or single surface planers, — combined surface/thickness planing machines with fixed cutterblock position, with an integrated feed in thicknessing mode, with or without demountable…

This document provides guidance on the range of tests that could be necessary to characterize soil and other soil materials intended to be re-used, with or without preliminary treatment (e.g. screening to remove over large material). It is intended to be of use in determining the suitability of soil materials for re-use (see 3.4.1), and the assessment of the environmental impacts that might arise…

1.1 Purpose The standard specifies the requirements for community-based organizations to deliver quality and safe health services to clients and families. The standard provides: • Community-based organizations with guidance on how to ensure quality and safety within their unique institutional context • Policy makers with a blueprint for the requirements to designate and recognize community-…

1.1 Scope This Recommendation | International Standard specifies the system layer of the coding. It was developed principally to support the combination of the video and audio coding methods defined in Parts 2 and 3 of ISO/IEC 13818. The system layer supports six basic functions: 1) the synchronization of multiple compressed streams on decoding; 2) the interleaving of multiple compressed…

1 Scope 1.1 Inclusions 1.1.1 This International Standard specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. NOTE Although the scope of this International Standard is limited to medical devices, it specifies requirements and provides guidance that might be applicable to other health care products. 1.1.2…

1 Scope This International Standard defines the ECMAScript Specification Suite containing the ECMAScript programming language and its required and optional built-in libraries. It defines all the necessary components (both normative and informative) that is needed to implement this suite of standards. This suite does not change if one or more components are updated by a new standard edition. The…