摘要 : Adequate medicine regulation requires nations to establish robust regulatory agencies that will subject all pharmaceutical products to pre- and postmarketing evaluation. These agencies are essential for any country wishing to ensu... 展开
作者 | Dario De Angelis Silvia Aiolli Stefano Gonnelli Anne Marie Georges Yauba Saidu |
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作者单位 | |
期刊名称 | 《Drug information journal》 |
总页数 | 9 |
语种/中图分类号 | 英语 / R9 |
关键词 | product registration developing nations medicine regulation National Regulatory Authority |
馆藏号 | N2008EPST0008378 |