Date

Monday, 22 April 2024 - Wednesday, 24 April 2024

Location

Online

Event summary

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);
  • 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.

Agenda

Share this page