eXtended EudraVigilance Medicinal Product Dictionary training course - September 2021

EventHumanRegulatory and procedural guidance

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Dáta

Dé Luain, 13 Meán Fómhair 2021, All day

Áit

Online
European Medicines Agency, Amsterdam, the Netherlands

Event summary

The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM) and 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 different types of medicinal products.

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