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Research / Drug safety / Pharmacology / European Medicines Agency / Pharmaceuticals policy / Committee for Medicinal Products for Human Use / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Pharmacovigilance / Serious adverse event / Clinical research / Pharmaceutical sciences / Pharmaceutical industry


25 SeptemberEMA/CHMPCommittee for Medicinal Products for Human Use (CHMP) Assessment report
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Document Date: 2014-12-17 05:29:48

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File Size: 2,74 MB

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