Extended EudraVigilance medicinal product dictionary (XEVMPD) training course for clinical trial sponsors - May 2023

Date

, -

Location

Online
European Medicines Agency, Amsterdam, the Netherlands

Event summary

This training focuses on:

  • Explaining the guidance and data elements necessary for the electronic submission of information on unauthorised medicinal products (referred to in the XEVMPD as 'development' products).
  • Applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM).
  • The use of the XEVMPD data entry tool (EVWEB). 

It includes exercises in the XEVPRM data entry tool (EVWEB) for the electronic submission and maintenance of development medicinal products.

Documents

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