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This document establishes a framework for identification and authentication systems. It provides recommendations and best practice that include: —    management and verification of identifiers; —    physical representation of identifiers; —    participants’ due diligence; —    vetting of all participants within the system; —    relationship between the unique identifier (UID) and possible…

This document specifies two procedures for the preparation of laboratory sheets prior to measuring optical properties. One is the preparation of pads in a Büchner funnel using a filter paper or a wire screen and the other one is the preparation of laboratory sheets in a standard sheet former (conventional or Rapid Köthen). This document is applicable to all wood pulps and to most other types of…

This document specifies a procedure for the detection of a DNA sequence of the open reading frame five (ORF V) from cauliflower mosaic virus (CaMV) and a procedure for the detection of the DNA sequence of the nopaline synthase (nos) gene from tumour-inducing (Ti) plasmids of phytopathogenic Rhizobium radiobacter (formerly named Agrobacterium tumefaciens). The procedures can be used in the context…

IEC TS 63383:2022 deals with cybersecurity related to measuring devices (PMD according to IEC 61557-12 and PQI according to IEC 62586-1) and devices for data collection (devices according to IEC 62974-1) that are intended to be installed in restricted access areas. This document deals with cybersecurity aspects (e.g. device hardening or device resilience) of device(s) used for power metering and…

IEC TR 62715-6-21:2022, which is a technical report, provides information about various folding types and hinge structures of foldable products which can affect the durability of a foldable panel. This document focuses only on the issues concerning the foldable products and will not include product parts that do not affect display durability such as speakers, batteries, communication ports.

This document defines the set of frameworks of consent for the collection, use and/or disclosure of personal information by healthcare practitioners or organizations that are frequently used to obtain agreement to process the personal health information of subjects of care. This is in order to provide an informational consent framework which can be specified and used by individual policy domains…

This document specifies the requirements for reference beta radiation fields produced by radioactive sources to be used for the calibration of personal and area dosemeters and dose-rate meters to be used for the determination of the quantities Hp(0,07), H'(0,07;Ω), Hp(3) and H'(3;Ω), and for the determination of their response as a function of beta particle energy and angle of incidence…

This document establishes general requirements and recommendations for service providers that offer guided or self-guided visits in order to enable visitors to learn: —    about the characteristics of the cultural, historical or natural value of a tourist site; or —    how a service, an activity or a product is developed now or was developed in the past (i.e industrial tourism). This document…

This document specifies a number of metadata elements that describe resources containing medical knowledge, primarily digital documents provided as web resources, accessible from databases or via file transfer, but can be applicable also to paper documents, e.g. articles in the medical literature. The metadata elements —    support unambiguous and international understanding of important aspects…

This document provides users of interactive systems with a summary of the existing knowledge about ergonomics considerations for the influence of artificial (electric) and natural lighting of environments on humans other than on vision, with a focus on non-image-forming effects. The document can furthermore be used as guidance on the specification of use environments in consideration of non-…