Abstract
This document provides guidelines on identification and labelling of medicinal products from the point of manufacture of packaged medicinal product to the point of dispensing the product.
This document outlines best practice for AIDC barcoding solutions for applications. Users can, however, consider the coding interoperability requirements for other AIDC technologies, e.g. Radio Frequency Identification (RFID).
General information
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Status: PublishedPublication date: 2020-09Stage: International Standard to be revised [90.92]
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Edition: 2Number of pages: 36
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Technical Committee :ISO/TC 215ICS :35.240.80
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Life cycle
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Previously
WithdrawnISO/TS 16791:2014
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Now
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Will be replaced by
Under developmentISO/DIS 16791