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

• Date:
  Thursday, 22 May 2014, All day
• Location:
  European Medicines Agency, Amsterdam, the Netherlands

The European Medicines Agency 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. Places are limited.

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): 6-7 February 2014, London, UK