Extended Medicinal Product Dictionary (xEVMPD)

All Marketing authorization holders within the European Union shall register their products in the xEVMPD database provided by EudraVigilance. The information to be supplied is increasing constantly and includes 

  • administrative infomation
  • details about the marketing authorisation and the product
  • copies of the SPC and PIL


Prior to entering any data, users are required to complete multi-hour training and pass EudraVigilance's xEVMPD knowledge evaluation.


Our staff has passed all trainings and evaluations and is experienced in dealing with EudraVigilance and xEVMPD. We coordinate with different departments within your company in order to collect the required information and take over the tedious task of

  • entering your products into the database and 
  • maintaining the data in a current state.