Digital living network alliance (DLNA) home networked device interoperability guidelines - Part 4: D...
IEC 62481-4:2014 describes the set of guidelines based on DLNA DRM Interoperability Solutions (DIS), which are defined as methods to enable the secure transfer and use of protected commercial content among different implementations on network media devices. This content could be protected by different content protection technologies. In this standard they are referred to as DRMs.
Language resource management — Semantic annotation framework (SemAF) — Part 5: Discourse structure (...
A discourse is a process of communication. ISO/TS 24617-5:2014 addresses how a discourse is structured in terms of its realization/presentation and content, and shows how its dual structure can be represented in a graph. The current specification focuses on the annotation of discourse structures in text only, but it can be extended to discourses in other modalities.
Nanomaterials — Preparation of safety data sheets (SDSs)
This Technical Report provides guidance on the development of content for, and consistency in, the
communication of information on safety, health and environmental matters in safety data sheets
(SDS) for substances classified as manufactured nanomaterials and for chemical products containing
manufactured nanomaterials. It provides supplemental guidance to ISO 11014:2009[1] on the preparation
of…
Medical electrical equipment — Part 2-26: Particular requirements for the basic safety and essential...
This Standard covers ME EQUIPMENT that is intended to be installed or used in accordance with
CSA C22.1, Canadian Electrical Code, Part I.
This particular standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of
ELECTROENCEPHALOGRAPHS (EEG) as defined in 201.3.63, hereafter referred to as
ME EQUIPMENT. This standard is applicable to ME EQUIPMENT used in a clinical environment
(e.g.,…
Medical electrical equipment - Part 1: General requirements for basic safety and essential performan...
Scope, object and related standards
1.1 * Scope
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that…
Medical electrical equipment — Part 2-47: Particular requirements for the basic safety and essential...
This Standard covers ME EQUIPMENT that is intended to be installed or used in accordance with
CSA C22.1, Canadian Electrical Code, Part I.
201.1 Scope, object and related standards
Clause 1 of the general standard1 applies, except as follows:
201.1.1 Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
AMBULATORY…
Medical electrical equipment — Part 2-55: Particular requirements for the basic safety and essential...
This Standard covers ME EQUIPMENT that is intended to be installed or used in accordance with
CSA C22.1, Canadian Electrical Code, Part I.
1 Scope
201.1 Scope, object and related standards
IEC 60601-1:2005, Clause 1 applies, except as follows:
201.1.1 * Scope
Replacement:
This International Standard specifies particular requirements for the BASIC SAFETY and ESSENTIAL
PERFORMANCE…
Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential per...
This Standard covers ME EQUIPMENT that is intended to be installed or used in accordance with
CSA C22.1, Canadian Electrical Code, Part I.
Subclause 1.1 of The general standard is replaced by:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PULSE OXIMETER
EQUIPMENT intended for use on humans, hereafter referred to as ME EQUIPMENT. This includes any part…
Medical electrical equipment — Part 2-16: Particular requirements for the basic safety and essential...
This Standard covers ME EQUIPMENT that is intended to be installed or used in accordance with
CSA C22.1, Canadian Electrical Code, Part I.
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as
HAEMODIALYSIS EQUIPMENT.
This International Standard does not take into…
Information technology — W3C Web Content Accessibility Guidelines (WCAG) 2.0
ISO/IEC 40500:2012 [Web Content Accessibility Guidelines (WCAG) 2.0] covers a wide range of recommendations for making Web content more accessible. Following these guidelines will make content accessible to a wider range of people with disabilities, including blindness and low vision, deafness and hearing loss, learning disabilities, cognitive limitations, limited movement, speech disabilities,…