药品标准物质
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在新药开发过程中,需要标定自己的药品标准物质。
PRM should be determinated during new drug development and research .
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新药开发研究过程中药品标准物质的标定
The Determination of Pharmaceutical Reference Materials During New Drug Development and Research
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药品标准物质分包装工作是标准物质全部工作中重要的组成部分。
The sub-packaging work of pharmaceutical standard material is an important part of the whole work of standard matter .
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前言:药品标准物质系指用于药物及其制剂的鉴别、检查、含量测定的标准物质。
Pharmaceutical reference materials ( PRM ) refer to the standard materials used in tests for identification , purity and assay of pharmaceuticals .
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生化药品标准物质是其质量控制体系的重要组成部分,也是当前药品质控研究的热点和重点之一。
The standard materials for the quality control of biochemical drugs are important , and also the hotspot and the emphasis in current pharmaceutical quality control study .