Date
- Thursday, 26 November 2015, All day
Location
- European Medicines Agency, Amsterdam, the Netherlands
This face-to face training course was prepared to facilitate the practical implementation of the requirements including technical aspects and all related procedures on electronic submission of information on medicines by marketing authorisation holders in the European Union (EU) and European Economic Area (EEA) countries outside the EU. The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products. Places limited.