Methods the 5 control strains recovery test validation method was used as described in the Chinese Pharmacopoeia 2005 edition.
方法按中国药典2005版有关规定,采用5种阳性对照菌回收率试验进行其方法学验证试验。
Objective to replace the developing agents benzene and toluene in thin-layer chromatography in the Chinese Pharmacopoeia 2005 Volume I.
目的替换《中国药典》(2005年版一部)薄层鉴别中使用苯和甲苯的展开剂。
Results: Each index is accorded with the quality level re - quest in Chinese Pharmacopoeia 2005 in the 2 years validity time.
结果:二年实际有效期内各项指标符合中国药典2005版质量标准要求。
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