Thursday, May 5, 2022 - 09:00 - 13:00 Amsterdam time (CEST)
Date
,
-
Location
Online
European Medicines Agency, Amsterdam, the Netherlands
Event summary
This training focuses on guidance:
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.