ISO/CD 13825:2024
Petroleum and related products

Standard No.
ISO/CD 13825:2024
Release Date
2024
Published By
International Organization for Standardization (ISO)  IX  /  ISO
Latest
ISO/CD 13825:2024
 

Introduction
This document provides guidelines and recommendations for the ethical use of extended reality (XR) technologies in educational settings. It aims to address the challenges and opportunities presented by XR in education, focusing on issues such as privacy, security, accessibility, and inclusivity. The report outlines best practices for educators, administrators, developers, and policymakers to ensure that the integration of XR into learning environments is both effective and ethically sound.

ISO/CD 13825:2024 history

Standard and Specification

AS/NZS IEC 60601.2.20:2022 (RLV) Medical electrical equipment, Part 2.20: Particular requirements for the basic safety and essential performance of infant transport incubators AS/NZS IEC 60601.2.20:2022 Medical electrical equipment, Part 2.20: Particular requirements for the basic safety and essential performance of infant transport incubators CAN/CSA-C22.2 NO.60601-2-47-2014(R2018) Medical electrical equipment — Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems BS EN 60601-2-24:2015 Medical electrical equipment. Particular requirements for the basic safety and essential performance of infusion pumps and controllers CAN/CSA-C22.2 NO.60601-2-43-2011(R2022) Medical electrical equipment — Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures CAN/CSA-C22.2 NO.60601-2-29-2010(R2018) CAN/CSA-C22.2 No. 60601-2-29-10 (Medical electrical equipment — Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators) CAN/CSA-C22.2 NO.60601-2-40-2017 Medical electrical equipment — Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment VDE 0750-2-33 E*DIN EN 60601-2-33:2008-10 Medical electrical equipment – Part 2-33: Particular requirements for basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 62B/706/CDV:2008) VDE 0750-2-34 E*DIN IEC 60601-2-34:2008-01 Medical electrical equipment – Part 2-34: Particular requirements for basic safety and essential performance of invasive blood pressure monitoring equipment (IEC 60601-2-34) VDE 0750-2-6 E*DIN IEC 60601-2-6:2010-02 Medical electrical equipment - Particular requirements for basic safety and essential performance of microwave therapy equipment (IEC 62D/808/CD:2009)



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