Regulatory approaches: Global medical device tracking advancement in USA, EU and India

G. Saini, M. Choudhary, V. Budhwar, Tarif Hussain
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Abstract

Advancement in science & technology of medical industry is coming up with innovations. Medical devices play a vital role. Real Time Location System (RTLS) which includes Radio Frequency Identification (RFID) device, Wi-Fi technology that helps to look after adverse events and recall products when required, thereby, prevent theft by keeping regular check on their movement with location sensors. In 19th century two products of United States faced product withdrawal. After that, US felt the need to develop system for product record management and tracking. In 2004, FDA introduced Unique Device Identifier (UDI) for medical device tracking. With time, GHTF came up with UDI working groups and in 2013, new version of UDI guidelines for globally harmonized use was generated. In this article study about various countries has been done. It was found that countries like United States and Europe have introduced medical device tracking system and by 2022 this will be implemented in India.
监管方法:美国、欧盟和印度的全球医疗器械跟踪进展
医疗行业的科技进步带来了创新。医疗设备起着至关重要的作用。实时定位系统(RTLS)包括射频识别(RFID)设备,Wi-Fi技术,有助于处理不良事件并在需要时召回产品,从而通过定期检查位置传感器的移动来防止盗窃。19世纪,美国的两种产品面临产品撤回。在那之后,美国觉得有必要开发产品记录管理和跟踪系统。2004年,FDA为医疗器械跟踪引入了唯一设备标识符(UDI)。随着时间的推移,GHTF成立了UDI工作组,并于2013年生成了全球统一使用的新版UDI指南。在这篇文章中,对各个国家进行了研究。据发现,美国和欧洲等国家已经引入了医疗器械跟踪系统,到2022年,印度将实施这一系统。
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