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Activités relatives aux services de l'eau potable...
This International Standard provides guidelines for the management of wastewater utilities and for the assessment of wastewater services. This International Standard is applicable to publicly and privately owned and operated...
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Ingénierie des systèmes et du logiciel — Processus...
1 Scope 1.1 Overview This document establishes a common framework for software life cycle processes, with well‐defined terminology, that can be referenced by the software industry. It contains processes, activities, and tasks...
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Industries du pétrole et du gaz naturel - Structures...
This part of ISO 19904 provides requirements and guidance for the structural design and/or assessment of floating offshore platforms used by the petroleum and natural gas industries to support the following functions: -...
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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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Stérilisation des produits de santé - Irradiation...
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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Stérilisation des produits de santé - Irradiation...
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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Ingénierie du logiciel et des systèmes — Exigences...
This document supports the interest of system users in having consistent, complete, accurate, and usable information. It addresses both available approaches to standardization: a) process standards, which specify the way that...
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Dispositifs médicaux — Application de la gestion...
1 Scope This document specifies terminology, principles and a process for risk management of medical devices , including software as a medical device and in vitro diagnostic medical devices . The process described in this...
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Mise en service des bâtiments et Check Sheets...
This is the first edition of CSA Z320, Building commissioning. This Standard provides guidelines for the commissioning of buildings and all related building systems, and has been developed to deal with buildings and/or their...
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Système de gestion de la prévention des incapacités...
The proposed Standard will develop and specify the requirements for a Work Disability Prevention Management System ( WDP-MS). The Standard will provide guidelines to: Develop a framework that will help to increase the ability...
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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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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...