eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course - October 2022
Event
Human
Regulatory and procedural guidance
Date
Location
The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on authorised and unauthorised (referred to in the XEVMPD as 'development') 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.