EMA has published version 2.1 of the Implementation Guide for the ISO IDMP standards, which provide standardised definitions for the identification and description of medicinal products for human use.
The new version reflects the latest agreements and details available, which supports the European medicines regulatory network to prepare for the implementation of Step 1 of the Product Management Service (#PMS).
Products Management Services – Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe: Introduction – EU Implementation Guide (PDF/334.92 KB) (updated)
First published: 11/02/2020
Last updated: 30/06/2021
EMA/676106/2019 Version 2.1