Measurement procedures for materials used in photovoltaic modules - Part 1-6: Encapsulants - Test me...
IEC 62788-1-6:2017+A1:2020 defines the terminology, test equipment, test environment, specimen preparation, test procedures, and test report for measuring the degree of cure of Ethylene-Vinyl Acetate (EVA) encapsulation sheet used in photovoltaic (PV) modules. The differential scanning calorimetry (both residual enthalpy and melt/freeze protocols) and gel content methods are included herein. This…
Procédures de mesure des matériaux utilisés dans les modules photovoltaïques - Partie 1-6: Encapsula...
L’IEC 62788-1-6:2017+A1:2020 définit la terminologie, l'équipement d'essai, l'environnement d'essai, la préparation des éprouvettes, les procédures d'essai et le rapport d'essai pour le mesurage du degré de durcissement de la couche d'encapsulation en éthylène-acétate de vinyle (EVA) utilisée dans les modules photovoltaïques (PV). Les méthodes de l'analyse…
Communication networks and systems for power utility automation - Part 90-4: Network engineering gui...
IEC TR 61850-90-4:2020(E), which is a Technical Report, is intended for an audience familiar with network communication and/or IEC 61850-based systems and particularly for substation protection and control equipment vendors, network equipment vendors and system integrators.
This document focuses on engineering a local area network limited to the requirements of IEC 61850-based substation…
Dispositifs médicaux de diagnostic in vitro — Exigences relatives aux protocoles d’harmonisation int...
Le présent document spécifie les exigences relatives à un protocole mis en œuvre par un organisme international pour obtenir des résultats équivalents entre au moins deux DMDIV pour un même mesurande en l'absence de procédures de mesure de référence et de matériaux de référence certifiés ou d'étalons internationaux conventionnels adaptés à l'usage prévu. Dans ce cas, le protocole d…
In vitro diagnostic medical devices — Requirements for international harmonisation protocols establi...
This document specifies requirements for a protocol implemented by an international body to achieve equivalent results among two or more IVD MDs for the same measurand for cases where there are no reference measurement procedures and no fit-for-purpose certified reference materials or international conventional calibrators. In this case, the harmonisation protocol defines the highest level of…
Healthy Enterprise — Prevention, Promotion, and Organizational Practices Contributing to Health and ...
This document provides the operating rules of the BNQ regarding the Healthy Enterprise certification program. It was prepared taking into consideration the latest versions of international accreditation requirements applicable to organizations providing audit and certification of management systems.
The Healthy Enterprise certification program is available to any type of enterprise or…
Entreprise en santé — Prévention, promotion et pratiques organisationnelles favorables à la santé et...
Le présent document prévoit les règles de fonctionnement du BNQ applicables au programme de certification Entreprise en santé. Il a été conçu en prenant en considération les dernières versions en vigueur des exigences d’accréditation internationales applicables aux organismes réalisant des audits ainsi que la certification de systèmes de gestion.
Le programme de certification Entreprise en santé…
Health informatics — Guidance on the identification and authentication of connectable Personal Healt...
The document gives guidance for managing healthcare service security using connectable personal health devices. This document considers unidirectional data uploading from the PHD to the gateway (manager device), however, there are many clinical use cases for bidirectional data exchange.
This document is applicable to identification and authentication between the bidirectionally connected PHDs and…
Intelligent transport systems — Vehicle interface for provisioning and support of ITS Services — Par...
This document specifies a conformance test for a UVIP server and client system developer assessment of self-conformance of the supplier's UVIP server and client system. The conformance test cases follow the use cases definition of ISO 13185-1 and the requirements stated in ISO 13185-2 and ISO 13185-3.
The purpose of this document is to provide information to the UVIP server and client system…
Nanotechnologies — Assessment of nanomaterial toxicity using dechorionated zebrafish embryo
This document specifies a method for rapidly assessing nanomaterial toxicity (fish early life stage, 0 HPF to 120 HPF). It includes information on the importance of acellular chorion removal, detailed chorion removal procedures, and a complete protocol for the toxicity assessment of nanomaterials using dechorionated zebrafish embryos. The focus of this document is on testing nanomaterial toxicity.
