Resumen
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).
Informaciones generales
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Estado: PublicadoFecha de publicación: 2020-09Etapa: Cierre de la revisión [90.60]
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Edición: 2Número de páginas: 36
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Comité Técnico :ISO/TC 215ICS :35.240.80
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Ciclo de vida
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Anteriormente
RetiradaISO/TS 16791:2014
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Ahora
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