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Date: 2013-10-09 08:55:57European Union Pharmaceutical industry Pharmaceutical sciences Government European Medicines Agency Directive 2001/83/EC Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Clinical research Research | EN Official Journal of the European UnionAdd to Reading ListSource URL: ec.europa.euDownload Document from Source WebsiteFile Size: 97,95 KBShare Document on Facebook |
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