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。
Conclusion: the garlic emulsion prepared by this composition and technology accords with the stipulation of Chinese Pharmacopoeia (2005).
结论：用该工艺制备的大蒜乳剂符合《中国药典》2005年版乳剂要求。
Objective To evaluate uncertainty for concentration of hydrochloric acid standard solution prepared and standardized with the method in Chinese Pharmacopoeia (edition 2005).
目的对按照2005年版《中国药典》方法配制和标定的盐酸标准溶液浓度进行不确定度评定。
Results the colony recovery of membrane filtration method meets the related regulations of Chinese Pharmacopoeia (2005 edition).
结果：薄膜过滤法的菌落回收率符合2005年版《中国药典(二部)》相关规定。
Result the method can compatible with the validation test of Chinese Pharmacopoeia 2005 version.
结果本方法满足中国药典2005版验证试验的基本要求。
The bacterial endotoxin testing method for Huangqi Injection was set up, by the bacterial endotoxin test was approved according to Chinese Pharmacopoeia 2005 edition.
建立黄芪注射液的细菌内毒素检查法。依据《中国药典》2005年版附录细菌内毒素检查法进行试验。
Methods Common methods in Chinese Pharmacopoeia(edition 2005) were used to cultivate culture media dilution, using recovery rate of the bacteria in the comparison experiment.
方法采用中国药典2005年版一部规定的常规法、培养基稀释法进行菌回收率比较试验。
Methods the method was based on the membrane filtration of sterility test of Chinese Pharmacopoeia 2005.
方法按《中国药典》2005年版附录无菌检查法项下薄膜过滤法。
The test method was carried out according to the method in volume two, Chinese Pharmacopoeia Edition 2005.
本试验参照《中国药典》2005年版二部无菌检查法进行试验。
CONCLUSION: the dispersible tablets prepared are in conformity with the standards specified in Chinese Pharmacopoeia (2005).
结论：该分散片符合《中国药典》2005年版的相关规定。
Methods We testified and checked the microbial limit with 2005 "Chinese Pharmacopoeia".
方法按中国药典2005年版一部微生物限度检查法进行验证和试验。
According to the "sterile test method" which is recorded in the appendix in Chinese Pharmacopoeia (2005 Edition), the methodology validation is experimented with Gentamycin sulfate injection.
本试验取硫酸庆大霉素注射液，按《中国药典》2005年版二部附录所载的“无菌检查法”项下进行方法学验证试验。
The quality of the slow-release of chlorine dioxide prepared with sodium carboxymethyl Cellulose and carbopol 940 as the main mixed-matrix consistent with the 2005 edition of Chinese Pharmacopoeia.
制备的以羧甲基纤维素钠与卡波姆940为主要混合基质的二氧化氯缓释凝胶剂质量符合2005年版《中国药典》凝胶项下的规定。
Objective to analyze the uncertainty of concentration of hydrochloric acid volumetric solution prepared and standardized according to the method in Chinese Pharmacopoeia (editor 2005).
目的对按照2005年版《中国药典》方法配制和标定盐酸滴定液浓度进行不确定度评价。
Through the validation of production equipment and process of medical oxygen, to ensure the produce quality in line within the request of edition 2, Chinese Pharmacopoeia 2005.
针对医用氧生产设备、工艺进行验证，确保产品质量符合《中国药典》二○○五版二部的要求。
CONCLUSION it is reasonable that the 2005 edition of Chinese Pharmacopoeia specifies that the medicinal part of Herba cum Radice Asari is...
结论2005年版的《中国药典》将细辛药用部位由全草改为根茎是合理的，穴贴定喘膏未检出马兜铃酸a。
Methods According to the "Chinese Pharmacopoeia"2005 edition testing different conditions 5-Qiangjia base furfural content different.
结果：不同季节不同降温条件、同一灭菌车上不同位置5-羟甲基糠醛含量不同。
Methods According to the "Chinese Pharmacopoeia"2005 edition testing different conditions 5-Qiangjia base furfural content different.
结果：不同季节不同降温条件、同一灭菌车上不同位置5-羟甲基糠醛含量不同。
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