Date
- Thursday, 19 March 2015, All day
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 eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) data-entry tool EVWEB. It includes exercises in the XEVPRM data-entry for the electronic submission and maintenance of different types of medicinal products. Places limited.