Data Recording for Responsible Robotics

Jon Skerlj, Maximilian Braun, Sophia Witz, Svenja Breuer, Marieke Bak, Sebastian Scholz, Abdeldjallil Naceri, Ruth Müller, S. Haddadin, Iris Eisenberger
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Abstract

The last decades have seen continuous attempts to advance the application of robotics and artificial intelligence (AI) research in several areas such as healthcare environments. However, using (semi)autonomous robots in healthcare also poses risks that need to be addressed throughout the systems' lifecycle. In this work, we present our version of a data recorder, as the output of an interdisciplinary research collaboration that addresses relevant social, ethical, legal, and technical aspects of advanced robotics in healthcare. We use social science insights from interviews and ethnographic fieldwork with relevant stakeholders as well as ethical and legal analyses to derive and implement four technical requirements for a data recorder to enhance accountability and transparency of a service humanoid robot, GARMI, assisting in healthcare. We present a tool to log and visualize data from human-robot interactions as a means of including non-expert users and other relevant stakeholders in accountability relationships, which also helps us to enhance the transparency of advanced robotics in general and to fulfill the examined requirements of the Medical Device Regulation (MDR) and the General Data Protection Regulation (GDPR).
负责任机器人的数据记录
在过去的几十年里,人们不断尝试推进机器人和人工智能(AI)研究在医疗保健环境等多个领域的应用。然而,在医疗保健中使用(半)自主机器人也会带来风险,需要在系统的整个生命周期中加以解决。在这项工作中,我们展示了我们的数据记录仪版本,作为跨学科研究合作的成果,解决了医疗保健中先进机器人的相关社会、伦理、法律和技术方面的问题。我们利用社会科学的见解,从访谈和民族志实地考察相关利益相关者以及道德和法律分析得出并实施数据记录仪的四项技术要求,以提高服务人形机器人GARMI的问责制和透明度,协助医疗保健。我们提供了一种工具,用于记录和可视化人机交互数据,作为包括非专业用户和其他相关利益相关者在内的问责关系的一种手段,这也有助于我们提高一般先进机器人的透明度,并满足医疗器械法规(MDR)和通用数据保护法规(GDPR)的审查要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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