Extended EudraVigilance medicinal product dictionary (XEVMPD) training course for clinical trial sponsors - February 2022
Table of contents
Date:
17/02/2022
Location:
Online, 13:30 - 18:15 Amsterdam time (CET)
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.