The problems of effective digits in the Chinese Pharmacopoeia are discussed.
讨论了《中国药典》中存在的有效数字问题。
CONCLUSIONS the dispersible tablets accord with the requirement of the Chinese Pharmacopoeia (2000). The method of quality control is reliable.
结论:该分散片符合中国药典2 0 0 0年版的规定,质量控制方法可靠。
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。
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。
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。
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。
Microbial limit tests were validated according to Chinese Pharmacopoeia Edition 2005.
按照《中国药典》2005版微生物限度检查方法进行验证试验。
METHODS:Heavy metals in the purified water were detected by the refined testing water specifically for detection in accordance with Chinese Pharmacopoeia .
方法:采用精制处理后的检查专用试验水,按《中国药典》方法检查纯化水中的重金属。
The rules of calculation of effective digits in expression of result of analysis are introduced. The problems of effective digits in the Chinese Pharmacopoeia are discussed.
介绍了有效数字的计算规则,对分析测试结果表达中的有效数字进行了介绍。讨论了《中国药典》中存在的有效数字问题。
The dissolution rates of prepared microencapsulated Dim chewing gums were evaluated by comparing with control samples abroad and non microencapsulated samples according to Chinese Pharmacopoeia 1995.
根据中国药典1995年版所载的溶出度测定方法测定其溶出度,并与国外同类产品及未包囊的糖胶片进行比较。
Through comparison with fungus inspection of a mercury-containing preparation, the composition can achieve the quality standard required by Chinese Pharmacopoeia on sterile products.
经过与含汞制剂的菌检比较,本发明组合物能达到中国药典对无菌制品要求的质量标準。