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 been recently updated the following chapters:
- Introduction
- Chapter 1: Registration requirements
- Chapter 7: Migration guide: migration rules between xEVMPD and PMS including backwards compatibility rules
OpenEdition vous propose de citer ce billet de la manière suivante :
vroby (4 octobre 2024). 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. ELSIBI. Consulté le 18 février 2026 à l’adresse https://doi.org/10.58079/12f90





