91 257 00 03 Chamada para a rede móvel nacional info@formiventos.com

10 January 2020
Information Management Division


This document provides an overview of the data management and quality assurance activities performed by the European Medicines Agency (hereafter “the Agency”) on information of suspected
adverse reactions and medicinal products reported to and held in EudraVigilance and the XEVMPD.


Detailed guide regarding the EudraVigilance data management activities by the European Medicines Agency