Date: 2014-12-17 05:29:48Research 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 reportAdd to Reading ListSource URL: www.ema.europa.euDownload Document from Source Website File Size: 2,74 MBShare Document on Facebook
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