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Date: 2015-11-08 06:14:30Pharmaceuticals policy Health Medical research Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Postmarketing surveillance Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance | COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume IAdd to Reading ListSource URL: www.myereport.euDownload Document from Source WebsiteFile Size: 386,06 KBShare Document on Facebook |
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