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医疗机构制剂检验基本操作指南
$50.19
本书以2010年版《中华人民共和国药典》附录收载的与制剂检验相关项目和方法为重点,系统介绍了药品检验实验室的基本要求和安全管理,制剂检验的方法原理、操作步骤、注意事项、操作示例、检验记录、问题处理等内容。本书内容丰富,图文并茂,科学性和实用性强,可帮助药学工作者和相关人员正确掌握药品检验操作。
傅小英,女,50岁,新疆人,副主任药师,国家实验室计量认证评审员,总后卫生部师职助理员,1989年毕业于新疆医科大学药学专业,长期在药品监督、检验和供应管理一线工作,具备丰富的实践经验。承担军队科研项目3项,发表学术论文20余篇,获军队科技进步三等奖2项,组织编写多期《全军药材监督管理文件汇编》,担任全军药学专业委员会药物分析分委会副主任委员等学术任职。
一 药品检验实验的基本要求及安全管理 二 分析天平与称量 三 一秀(常用)检查法 四 滴定分析法 五 旋光度测定法 六 紫外-可见分光光度法 七 薄层色谱法 八 高效液相色谱法 九 微生物检验一般要求 十 无菌检查法 十一 微生物限度检查法 十二 细菌内毒素检查法 十三 学溶性微粒检查法 十四 实时溶出度测定法 十五 药品快速检验法 十六 中成药中非法添加化学药物的检测方法 十七 药物分析中的有效数字 附录A 检验记录与检验报告书的书写细则 附录B 常用玻璃器检定规程 附录C 常用培养基的制备方法 附录D 医药工业洁净室(区)悬浮粒子、浮游菌和沉降菌的测试方法《中华人民共和国国家标准》
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