EMA Updates User Manual for XEVMPDweb
Recommendation

4/5 November 2026
How to avoid Mix-Ups, Contamination and labelling issues
On 05 October 2026, the European Medicines Agency (EMA) published version 3 of the User manual for the eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) user interface (XEVMPDweb) (Reference Number: EMA/389113/2025).
The manual is intended for marketing authorisation holder and sponsor organisation users.
The update, dated 15 September 2026, follows Version 2 from July 2026 and reflects changes implemented in the XEVMPDweb production environment in September 2026.
According to the "Summary of changes" section, the following points were changed:
- "3.5.1. Add next page of results: Added as new section
- 3.5.5. Export: Content updated
- 3.5.8. Move to next/previous page of results: Added as new section
- 3.5.9. Move to top of the page: Added as new section
- The list of 'Fields' in 'Owned Authorised Products' and 'Authorised Products (Valid version)' advanced queries was expanded to include 'Authorisation/Renewal date'; screenshot on page 113 was updated"
The manual is available for download on the EMA website under Extended EudraVigilance medicinal product dictionary (XEVMPD) training.
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