This document provides requirements on identification and labelling of medicinal products from the point of manufacturing of packaged medicinal product to the point of dispensing the product.
This document outlines commonly accepted international practices for automatic identification and data capture (AIDC) barcoding solutions for applications and applies to manufacturers, distributors, healthcare facilities and all parties involved in labelling and distribution of packaged medicinal products. These users can, however, consider the coding interoperability requirements for other AIDC technologies, e.g. radio frequency identification (RFID); that technology is not addressed in this document except as for information.
PUBLISHED
SRPS CEN ISO/TS 16791:2020
PROJECT
dnaSRPS EN ISO 16791:2026
50.60
Close of voting. Proof returned by secretariat
Feb 26, 2026