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L'ISO 21504:2015 fournit des recommandations concernant les principes de management de portefeuille de projets et programmes. L'ISO 21504:2015 s'adresse à tous les types d'organismes, qu'ils soient publics ou privés, quels que soient leur taille ou leur secteur d'activité. Les recommandations fournies dans l'ISO 21504:2015 sont destinées à être adaptées à l…

ISO 21504:2015 provides guidance on the principles of project and programme portfolio management. ISO 21504:2015 is relevant to any type of organization including public or private and any size organization or sector. The guidance presented in ISO 21504:2015 is intended to be adapted to suit the specific environment of the project and programme portfolio. ISO 21504:2015 does not provide guidance…

1.1 This Standard applies to newly produced automatic valves (see Clause 3, Definitions) constructed entirely of new, unused parts and materials. These valves may be individual automatic valves or valves utilized as parts of automatic gas ignition systems. This Standard also applies to commercial/industrial safety shutoff valves (see Clause 3), herein after referred to as C/I valves. This…

1 Scope This Standard applies to the safety of such equipment designed and constructed for installation and use in accordance with CSA C22.1, Canadian Electrical Code, Part I (CE Code, Part I). This clause of Part 1 is replaced by the following. This International Standard deals with the safety of electric appliances for use with aquariums and garden ponds for household and similar…

IEC 62304:2006+A1:2015 Defines the life cycle requirements for medical device software. The set of processes, activities, and tasks described in this standard establishes a common framework for medical device software life cycle processes. Applies to the development and maintenance of medical device software when software is itself a medical device or when software is an embedded or integral part…

IEC 62061:2005+A1:2012+A2:2015 specifies requirements and makes recommendations for the design, integration and validation of safety-related electrical, electronic and programmable electronic control systems (SRECS) for machines (see Notes 1 and 2). It is applicable to control systems used, either singly or in combination, to carry out safety-related control functions on machines that are not…

L'IEC 62061:2005+A1:2012+A2:2015 spécifie les exigences et donne des recommandations pour la conception, l'intégration et la validation des systèmes de commande électriques, électroniques et électroniques programmables relatifs à la sécurité (SRECS) pour les machines (voir Notes 1 et 2). Elle s'applique aux systèmes de commande utilisés, séparément ou en combinaison, pour assurer…

IEC 62304:2006+A1:2015 Defines the life cycle requirements for medical device software. The set of processes, activities, and tasks described in this standard establishes a common framework for medical device software life cycle processes. Applies to the development and maintenance of medical device software when software is itself a medical device or when software is an embedded or integral part…

L'IEC 62304:2006+A1:2015 définit les exigences du cycle de vie des logiciels de dispositifs médicaux. L'ensemble des processus, activités et tâches décrit dans la présente norme constitue un cadre commun pour les processus du cycle de vie des logiciels de dispositifs médicaux. S'applique au développement et à la maintenance des logiciels de dispositifs médicaux lorsque le logiciel…

IEC 62841-2-14:2015 applies to hand-held planners the rated voltage is not more than 250 V for single-phase a.c. or d.c. tools, and 480 V for three-phase a.c. tools. The rated input is not more than 3 700 W. The limits for the applicability of this standard for battery tools is given in Annex K. This standard deals with the hazards presented by tools which are encountered by all persons in the…