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从中国药典 2005 年版的变更谈化学药品注册标准的规范书写………………………108<br />
对注册批件中生产工艺内容要求的思考………………………………………..………111<br />
工艺研究与申报资料中常见问题分析…………………………………..………………113<br />
化学药品注册标准中贮藏条件的规范书写………………………..……………………115<br />
浅谈我国药品质量控制模式的变迁………………………………………..……………117<br />
药品研发中多晶型问题浅议………………………………………………..……………120<br />
元素分析中的常见问题分析………………………………………..……………………123
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