SN-CEN/TR 17622:2021
建筑环境的可访问性和可用性 符合性评估

Accessibility and usability of the built environment – Conformity assessment


标准号
SN-CEN/TR 17622:2021
发布
2021年
发布单位
SCC
当前最新
SN-CEN/TR 17622:2021
 
 
适用范围
  Full Description ADOPTED_FROM:CEN/TR 17622:2021 This document provides criteria to assess conformity of the built environment with the functional requirements and recommendations described in EN 17210 Accessibility and usability of the built environment – Functional requirements, regardless of whether self-declaration, second-party attestation or third-party certification is requested. This document provides guidance on how and when accessibility and usability of the built environment have to be considered throughout all stages of the building process, including feasibility, design, construction, completion and post occupancy. It is also applicable for refurbishment or adaptation of existing buildings. FprCEN/TR 17621 Accessibility and usability of the built environment - Technical performance criteria and specifications, provides examples of a way or ways in which the functional requirements in EN 17210 could be fulfilled. Alternatively, National Standards or Regulations can determine the technical performance criteria and specifications to fulfil the functional requirements of/in EN 17210. NOTE 1 Design for All, Inclusive Design and Universal Design share a similar inclusive design philosophy. “Universal Design” means the design of products, environments, programmes and services to be usable by all people, to the greatest extent possible, without the need for adaptation or specialized design. “Universal Design” does not exclude assistive options or devices for particular groups of persons with disabilities where this is needed. NOTE 2 Terms such as \"design for all\", “inclusive Design”, \"universal design\", \"accessible design\", \"barrier-free design\", \"inclusive design\" and \"transgenerational design\" are often used interchangeably with the same meaning.

SN-CEN/TR 17622:2021相似标准


推荐

疫情时期可用性测试安全策略操作

b)法规背景   无论在哪个市场,德国医疗器械法案(MPG)都要求制造商识别管理由不良可用性造成风险。   IEC 62366-1没有规定形成性评价强制方法。这意味着即使没有真实用户参与评估也可以符合标准要求。而与之相反是,FDA在其人因工程指南中,建议“用户”参与。   对于总结评估,法规坚持要求对测试用户进行“真正可用性测试”。...

电能质量分析仪LINAX PQ5000 MOBILE功能升级

利用我们全新 LINAX PQ5000-Mobile电能质量分析仪,可以从用户侧验证电能质量供应状况:■ 电能质量■ 供电可用性■ 供电变更或改进后评估■ 能源流动分析 这个测量解决方案支持由配置管理器提供多达20个存储设备设置活动(在同一位置重复测量),可以提供用于连接移动设备WLAN接入点,并提供所有数据通过设备自己网站进行评估。...

医疗器械MDR可用性需求重要与作用范围

B)附录1,第3段:分析合理预见误使用(foreseeable misuse)   附录1第三段是一般安全性能需求,包含了更具体可用性需求:它要求制造商有一个风险管理体系。并且用以 “估计评估与预期使用合理预见误用reasonably foreseeable misuse)相关风险”。   这种风险分析必须符合当前技术水平。因此,纯粹推测是不够。...

梅特勒-托利多Signature金属检测机接口升级

采用升级后 Signature 金属检测机, 食品生产商不仅提高了生产效率竞争力,还可减少生产成本,并且符合当地全球食品安全标准,包括英国零售商协会 (BRC)、 国际食品标准 (IFS) 食品安全体系认证 (FSSC) 22000。更新时长不足 2 小时,最大限度缩短停机时间,并且无需将机器从生产线取下。        ...





Copyright ©2007-2022 ANTPEDIA, All Rights Reserved
京ICP备07018254号 京公网安备1101085018 电信与信息服务业务经营许可证:京ICP证110310号