European Medicines Agency information day on services and systems in pharmacovigilance: preparing for business change

Date

Monday, 7 December 2015, All day

Location

European Medicines Agency, Amsterdam, the Netherlands

The aim of this information day is to update marketing-authorisation holders on the enhancements of the EudraVigilance system and to help them prepare for business changes to come. The European Medicines Agency will discuss its recently published EudraVigilance stakeholder change management plan with marketing-authorisation holders. Detailed discussion will also take place on new functionalities for adverse drug reaction reporting, medical literature monitoring, the database of medicinal products (Article 57) as well as the central repository for periodic safety update reports.

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