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).

Begin

2024-06-26

WI

00251420

Planned document number

DIN EN ISO 16791

Project number

17600103

Responsible national committee

NA 176-02-03 AA - Terminology  

Responsible european committee

CEN/TC 251/WG 1 - Enterprise and Information  

Responsible international committee

ISO/TC 215/WG 6 - Pharmacy and medicines business  

previous edition(s)

Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020); German version CEN ISO/TS 16791:2020
2021-02

Order from DIN Media