Date

Thursday, 19 September 2019

Location

European Medicines Agency, Amsterdam, the Netherlands

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.

Documents

Agenda and registration form - eXtended EudraVigilance Medicinal Product Dictionary face-to-face training course (Amsterdam)

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