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).
PUBLISHED
CEN ISO/TS 16791:2020
IN_DEVELOPMENT
prEN ISO 16791 rev
10.99
New project approved
Jun 22, 2024