EMA: Update of the IRIS Guide
In December 2024 and January 2025, the "IRIS guide for applicants" was updated once more and is now valid in version 3.6. Like the "IRIS guide to registration and RPIs", the latest version of this document can be checked on the EMA website.
In addition to formal changes, some passages have been revised and re-linked with the latest updates. In line with the document history, minor adjustments have been made to the content of chapters 2. Common operations for all submission types, 7. Inspections and 12. Product Lifecycle Management (PLM) procedures. In contrast, chapters 4. Scientific Advice, 11. Parallel distribution notifications and 13. Paediatric medicines development were subject to more extensive revisions.
The latest versions of the IRIS documents can be found here:
- IRIS guide to registration and RPIs (Version 2.16)
- IRIS guide for applicants (Version 3.6)
Related GMP News
21.10.2026EMA Clarifies ESMP Reporting for Critical Medicine Shortages
20.10.2026EDQM Updates Guidance on CEP Sister File Applications
20.10.2026EDQM Revises Guidance on Electronic Submissions for CEP Applications
14.10.2026Bioassays in the United States Pharmacopoeia - Two Chapters come into Force in Spring
07.10.2026CEP 2.0: EDQM Updates Guidance on the Use of Certificates of Suitability
23.09.2026IRIS Portal: EMA expands digital Procedure Management



