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Date: 2013-10-09 09:07:11European Medicines Agency Government Pharmaceutical sciences Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Clinical research Pharmaceuticals policy Research | Microsoft Word - EMEA comments on draft RegulationAdd to Reading ListSource URL: ec.europa.euDownload Document from Source WebsiteFile Size: 204,36 KBShare Document on Facebook |
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