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Stérilisation des produits de santé - Exigences...
1.1 Inclusions 1.1.1 This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process...
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Systèmes aériens
Overview The Canadian Electrical Code is published in several parts, with Part III standards covering electrical protection, safety, and design criteria related to both overhead and underground systems for distribution and...
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Ingénierie du logiciel - Lignes directrices pour...
This International Standard specifies requirements for a quality management system when an organization: a) needs to demonstrate its ability to consistently provide products and services that meet customer and applicable...
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Mise en service des établissements de santé
1.1 General 1.1.1 This Standard provides requirements for the commissioning of health care facilities and all related building systems. It applies to new facilities, and renovations and additions to existing facilities. This...
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Ingénierie des systèmes et du logiciel - Profils...
This document provides a profile specification for the organizational management profile. The organizational management profile applies to VSEs involved in systems engineering and/or software engineering development. This...
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Sang et produits sanguins labiles
1.1 This Standard provides management requirements for facilities that collect, process, store, and use human blood and blood components for transfusion. It addresses issues of safety, efficacy, and quality for recipients...
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Ingénierie des systèmes et du logiciel - Gestion...
This standard establishes the requirements for systems engineering activities to be performed on projects of the United States (US) Department of Defense (DoD) and other defense agencies across the entire system life cycle...
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Ingénierie de systèmes et de logiciels - Profils...
ISO/IEC 29110:2015 is applicable to Very Small Entities (VSEs). VSEs are enterprises, organizations, departments or projects having up to 25 people. The lifecycle processes described in the set of International Standards (IS)...
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Stérilisation des produits de santé - Rayonnement...
1.1 This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO 11137 is limited to...
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Technologies de l'information - Systèmes bureautiques...
ISO/IEC 10175 consists of three parts: Part 1: Abstract service definitions and procedures Part 2: Protocol specification Part 3: Management abstract service definition and procedures This part of ISO/IEC 10175: - specifies a...
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Technologies de l'information - Méthodes d'essai...
This part of ISO/IEC 18046 defines test methods for performance characteristics of RFID systems for item management, and specifies the general requirements and test requirements for systems which are applicable to the...
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Technologies de l'information - Cloud computing...
This document provides a description of a set of common technologies and techniques used in conjunction with cloud computing. These include: virtual machines (VMs) and hypervisors; containers and container management systems...
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