EudraVigilance training on electronic reporting of individual case safety reports in the European Economic Area

• Date:
  Monday, 19 May 2014, All day
• Location:
  European Medicines Agency, Amsterdam, the Netherlands

The EudraVigilance training programme is open to contract research organisations (CROs), consultants and other organisations with an interest in the EudraVigilance project. Participants who pass the knowledge evaluation following the course will receive a notification from the European Medicines Agency that will allow them to register with EudraVigilance and to report ICSRs to the European Medicines Agency and/or the National Competent Authorities in the EEA.

Documents

Overview of the EudraVigilance training on electronic reporting of ICSRs in the EEA: 19-21 May 2014, London, UK