ISO/DIS 16791

This Draft International Standard is in the enquiry phase with ISO members.

Will replace ISO/TS 16791:2020

ISO/DIS 16791

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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

Status
: Under development

You can help develop this draft international standard by contacting your national member

Stage
: DIS ballot initiated: 12 weeks [40.20]
Edition
: 3

Number of pages
: 38
Technical Committee :
ISO/TC 215

ICS :
35.240.80
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