EMA发布XEVMPDweb用户手册第3版(EMA/389113/2025)
EMA Updates User Manual for XEVMPDweb
EMA于2026年10月5日发布XEVMPDweb用户手册第3版(编号EMA/389113/2025),该版本日期为2026年9月15日,接替2026年7月的第2版,反映XEVMPDweb生产环境在2026年9月的变更。
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.
来源:ECA GMP News · gmp-compliance.org