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Date: 2014-10-02 03:41:28 Research Health Pharmacology European Medicines Agency Pharmaceutical industry Pharmacovigilance Directive 65/65/EEC Summary of Product Characteristics Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceutical sciences Pharmaceuticals policy		EUROPEAN COMMISSION Brussels, [removed]COM[removed]final[removed]COD) Add to Reading List Source URL: ec.europa.eu Download Document from Source Website File Size: 429,95 KB Share Document on Facebook

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