The European Medicines Agency (EMA) prepared a pharmacovigilance information day focusing on Eudravigilance, adverse drug reaction reporting and signal management, medical literature monitoring, database of medicinal products (Article 57), Periodic Safety Update Report (PSUR) Repository etc.
Di Renzo Regulatory Affairs attended the event, which was held at the European Medicines Agency, in London, on the 28th of April 2015. Please see the list of next events in order to book another meeting in a location suitable for you.