eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course - June 2026

EventHumanRegulatory and procedural guidance

Date

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Location

Online

Event summary

The training focuses on:

  • explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on authorised and unauthorised (referred to in the XEVMPD as 'development') medicinal products;
  • applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM);
  • the use of the XEVMPD User Interface (XEVMPDweb).

It includes exercises in the XEVMPD User Interface (XEVMPDweb) for the electronic submission and maintenance of development medicinal products.

Documents

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