药品标准物质

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 .

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

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 .

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 .

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 .