医药信息学要求国际机器可读编码的药品包装标识

[中文适用范围]： 本文件规定了从包装药品生产制造至药品调配分发过程中，药品标识与标签的相关要求。本文件阐述了适用于包装药品标识与分发的自动识别与数据采集（AIDC）条码解决方案的通用国际实践，适用于药品制造商、分销商、医疗机构以及所有参与药品标签与流通的各方。不过，这些用户亦可考虑其他AIDC技术（如射频识别RFID）的编码互操作性要求；除作为信息参考外，本文件未对RFID技术作进一步阐述。 [外文原描述]： This document provides requirements on identification and labelling of medicinal products from the point of manufacturing of packaged medicinal product to the point of dispensing the product. This document outlines commonly accepted international practices for automatic identification and data capture (AIDC) barcoding solutions for applications and applies to manufacturers, distributors, healthcare facilities and all parties involved in labelling and distribution of packaged medicinal products. These users can, however, consider the coding interoperability requirements for other AIDC technologies, e.g. radio frequency identification (RFID); that technology is not addressed in this document except as for information.