Training on electronic submission of information on medicines - new pharmacovigilance legislation (Art. 57, paragraph 2, 2nd sub-paragraph, Regulation (EC) No. 726/2004)

• Date:
  Thursday, 20 March 2014, All day
• Location:
  European Medicines Agency, Amsterdam, the Netherlands

The EMA has prepared this eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) course 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.

Documents

Overview of the training on electronic submission of information on medicines - new pharmacovigilance legislation (Art. 57, paragraph 2, 2nd sub-paragraph, Regulation (EC) No. 726/2004): 20-21 March, Madrid, Spain