Systèmes de management de l'énergie — Exigences et recommandations pour la mise en oeuvre
Le présent document spécifie les exigences pour établir, mettre en œuvre, entretenir et améliorer un système de management de l'énergie (SMÉ). Le but recherché est de donner la possibilité à un organisme de parvenir, par une démarche méthodique, à l'amélioration continue de sa performance énergétique et du SMÉ.
Le présent document:
a) est applicable à tout organisme quel que soit son…
Greenhouse gases — Carbon footprint of products — Requirements and guidelines for quantification
This document specifies principles, requirements and guidelines for the quantification and reporting of the carbon footprint of a product (CFP), in a manner consistent with International Standards on life cycle assessment (LCA) (ISO 14040 and ISO 14044).
Requirements and guidelines for the quantification of a partial CFP are also specified.
This document is applicable to CFP studies, the results…
Energy management systems — Requirements with guidance for use
This document specifies requirements for establishing, implementing, maintaining and improving an energy management system (EnMS). The intended outcome is to enable an organization to follow a systematic approach in achieving continual improvement of energy performance and the EnMS.
This document:
a) is applicable to any organization regardless of its type, size, complexity, geographical…
Gasoline engines with direct fuel injection (GDI engines) — Installation of the high pressure fuel p...
This document specifies dimensions required for the installation and integration of the high pressure fuel pump in gasoline (GDI) engines. The location of the fuel connections and the dimensions of the pump outside shape are not defined since they vary according to the manufacturer of the pump and to the particular application.
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management p...
This document specifies:
— the general principles governing the biological evaluation of medical devices within a risk management process;
— the general categorization of medical devices based on the nature and duration of their contact with the body;
— the evaluation of existing relevant data from all sources;
— the identification of gaps in the available data…
Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais au sein d'un pr...
Le présent document spécifie:
— les principes généraux sur lesquels repose l'évaluation biologique des dispositifs médicaux dans un processus de gestion du risque;
— la classification générale des dispositifs médicaux, fondée sur la nature et la durée de leur contact avec le corps humain;
— l'évaluation de toutes les données pertinentes existantes;
—…
Rotating electrical machines - Part 14: Mechanical vibration of certain machines with shaft heights ...
IEC 60034-14:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC 60034-14:2018 specifies the factory acceptance vibration test procedures and vibration limits for certain…
Insulating liquids - Determination of the breakdown voltage at power frequency - Test method
IEC 60156:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC 60156:2018 specifies the method for determining the dielectric breakdown voltage of insulating liquids at power…
