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Date: 2014-09-10 03:29:20Research 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, XXX […](2014) XXX draftAdd to Reading ListSource URL: ec.europa.euDownload Document from Source WebsiteFile Size: 733,28 KBShare Document on Facebook |