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Date: 2016-07-29 02:05:14Pharmaceuticals policy Clinical research Clinical pharmacology Drug safety Healthcare quality Pharmacovigilance Clinical trial Medical device Pharmaceutical industry in China Adverse effect | Microsoft Word - GVP遵守通知.docAdd to Reading ListSource URL: www.pmda.go.jpDownload Document from Source WebsiteFile Size: 63,11 KBShare Document on Facebook |