EMA - PMS - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe: Updates of the EU Implementation Guide

The EU IDMP Implementation Guide (EU IG) for the submission of data on medicinal products defines the implementation requirements of the ISO IDMPstandards for the EU. The EU IG is the basis for submitting and exchanging medicinal product data in the EU. Its purpose is to enable stakeholders to prepare for the implementation of ISO IDMP standards in EU. It provides information on the following: Timelines Requirements Process Technical specification Data elements Associated business rules Have...