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Etiquetas: 1 January to 31 December 2013, 2013, adverse reaction reports, Annual Report on EudraVigilance for the European Parliament, Communication, Data analysis, Data collection and data qualit, Development of new functionalities, Drug, EMA, EudraVigilance, EudraVigilance for the European Parliament, European Medicines Agency, Health, Issue, London, reacciones adversas a medicamentos, salud, Sanidad, Substance, Training, Transparency, Tyo of recuester, Typ of request.
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