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Pharmaceuticals 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 I
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Document Date: 2015-11-08 06:14:30

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