ISO/IEC 20071-5:2022

International Standard   Current Edition · Approved on 10 May 2022

Information technology — User interface component accessibility — Part 5: Accessible user interfaces for accessibility settings on information devices

ISO/IEC 20071-5:2022 Files

English 29 Pages
Current Edition
BHD 72.45

ISO/IEC 20071-5:2022 Scope

This document specifies requirements and recommendations for making accessibility settings accessible and usable. It provides guidance on specific accessibility settings, saving settings and modifying settings. It specifies how to access and operate the accessibility setting mode, and how to directly activate specific accessibility features.

This document applies to all operating system user interfaces on all types of information and communications technologies (ICTs) from the point where the operating system is fully functional and waiting for the user to interact with it.

This document does not apply to:

—    storing and retrieving information from a stored user profile, including personally identifiable information;

—    accessibility of the closed functionality that does not support access by assistive technology;

—    accessibility of boot mode.

Best Sellers

GSO 150-2:2013
 
Gulf Standard
Expiration dates for food products - Part 2 : Voluntary expiration dates
BH GSO 150-2:2015
GSO 150-2:2013 
Bahraini Standard
Expiration dates for food products - Part 2 : Voluntary expiration dates
GSO 9:2022
 
Gulf Technical Regulation
Labeling of prepackaged food stuffs
BH GSO 9:2023
GSO 9:2022 
Bahraini Technical Regulation
Labeling of prepackaged food stuffs

Recently Published

ISO 18615-1:2026
 
International Standard
Traditional Chinese medicine — Electric radial pulse tonometric devices — Part 1: General requirements
ISO 21388-1:2026
 
International Standard
Acoustics — Hearing aid fitting management (HAFM) — Part 1: General process
ISO 20915:2026
 
International Standard
Life cycle inventory calculation methodology for steel products
ISO 11607-3:2026
 
International Standard
Packaging for terminally sterilized medical devices — Part 3: Requirements for process development for forming, sealing and assembly