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Global Medical Device Nomenclature: The Concept for Reducing Device-Related Medical Errors

机译:全球医疗设备术语:减少与设备有关的医疗错误的概念

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摘要

In the medical device field, there are a number of players, having quite different responsibilities and levels of understanding of the processes, but all with one common interest, that of ensuring the availability of sound medical devices to the general public. To assist in this very important process, there is a need for a common method for describing and identifying these medical devices in an unambiguous manner. The Global Medical Device Nomenclature (GMDN) now provides, for the first time, an international tool for identifying all medical devices, at the generic level, in a meaningful manner that can be understood by all users. Prior to the GMDN, many nomenclature systems existed, all built upon different structures, and used locally or nationally for special purposes, with unusual approaches. These diverse systems, although often workable in their own right, have had no impact on improving the overall situation of providing a common platform, whereby, medical devices could be correctly identified and the related data safely exchanged between the involved parties. Work by standard organizations such as, CEN (European Committee for Standardization) and ISO (International Organization for Standardization), from 1993 to 1996, resulted in a standard that specified a structure for a new nomenclature, for medical devices. In this article we are trying to explain GMDN as the prime method to reduce medical device errors, and to understand the concept of GMDN, to regulate the medical device throughout the globe. Here we also make an attempt to explain various aspects of the GMDN system, such as, the process of development of the GMDN-CEN report, purpose, benefits, and their structural considerations. In addition, there will be an explanation of the coding system, role of the GMDN agency, and their utilization in the unique device identification (UDI) System. Finally, the current area of focus and vision for the future are also mentioned.
机译:在医疗器械领域,有许多参与者,其职责和对过程的理解水平各有不同,但所有人都有共同的兴趣,即确保向公众提供健全的医疗器械。为了协助这一非常重要的过程,需要一种明确的方法来描述和识别这些医疗器械的通用方法。现在,全球医疗器械术语(GMDN)首次提供了一种国际工具,以有意义的方式在通用级别上识别所有医疗器械,所有用户都可以理解。在GMDN之前,存在许多命名系统,它们都建立在不同的结构上,并以不寻常的方法在本地或全国范围内用于特殊目的。这些多样化的系统虽然通常可以单独使用,但对改善提供通用平台的总体状况没有任何影响,因此可以正确识别医疗设备,并在相关各方之间安全地交换相关数据。 CEN(欧洲标准化委员会)和ISO(国际标准化组织)等标准组织从1993年到1996年的工作产生了一个标准,该标准指定了用于医疗设备的新术语的结构。在本文中,我们试图将GMDN解释为减少医疗器械错误的主要方法,并了解GMDN的概念,以规范全球医疗器械。在这里,我们还尝试解释GMDN系统的各个方面,例如GMDN-CEN报告的开发过程,目的,收益及其结构性考虑。此外,还将对编码系统,GMDN代理的作用及其在唯一设备标识(UDI)系统中的用法进行解释。最后,还提到了当前的重点领域和对未来的展望。

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