Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers
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 rev
Project number
17600103
Responsible national committee
Responsible european committee
CEN/TC 251/WG 1 - Enterprise and Information
Responsible international committee
ISO/TC 215/WG 6 - Pharmacy and medicines business
