eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course - May 2022
Event
Human
Regulatory and procedural guidance
Date
- Monday, 2 May 2022, All day
Location
- OnlineEuropean 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.