Extended EudraVigilance medicinal product dictionary (XEVMPD) training course for clinical trial sponsors - November 2022

EventHumanMedicines

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Date

, -

Sede

Online
European Medicines Agency, Amsterdam, the Netherlands

Event summary

This training focuses on:

  • Explaining the guidance and data elements necessary 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.

Registration

Documents

Programme and registration form - eXtended EudraVigilance Medicinal Product Dictionary live virtual training course for sponsors - September, October, November 2022

English (EN) (635.41 KB - PDF)

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