pharmacopoeia造句
- 1. The method in pharmacopoeia should be improved.
- 建议药典改进其方法。
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- 2. In Canada, the British Pharmacopoeia, BP, sets similar standards.
- 加拿大使用《英国药典》规定了类似的标准。
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- 3. The calcium lactate by extraction could reach pharmacopoeia standard.
- 萃取后乳酸钙中铁盐含量达到药典标准。
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- 4. Method: Analyzing the content of volatile oil by pharmacopoeia method.
- 方法：用药典方法对挥发油进行含量测定。
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- 5. There is no evident difference compared with Chinese Pharmacopoeia method.
- 并将此法与中国药典法进行差别检验，无显著差异。
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- 6. 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。
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- 7. Water, air, and cleanliness are the chief articles in my pharmacopoeia. — Napoleo.
- 水、空气和清洁是我药典上的主要条目。
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- 8. To testify and check with the microbial limit test of 2005 "Chinese Pharmacopoeia".
- 按《中国药典》(2005年版)微生物限度检查法进行验证和试验。
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- 9. Do you validate all analytical methods, and what do you do for the pharmacopoeia methods?
- 您是否验证了所有的分析方法？对于药典方法，您是怎么做的？
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- 10. The General Notices apply to all monographs and other texts of the European Pharmacopoeia.
- 凡例的内容适用于各论和欧洲药典中的其它章节。
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- 11. The General Notices apply to all monographs and other texts of the European Pharmacopoeia.
- 这句话应译为：总体概述适用于欧洲药典中所有的专论以及其它的正文。
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- 12. The new edition of the Pharmacopoeia marks a new stage in China's pharmaceutical standards.
- 新版药典的颁布标志着中国的药品标准水平再上一个新台阶。
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- 13. 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。
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- 14. Technological process and production conformed to china veterinary pharmacopoeia (1990 Edition).
- 生产工艺和产品符合《中国兽药典》（1990年版）要求。
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- 15. The synthetic technique of pharmacopoeia grade DL-malic acid through orthogonal test was studied.
- 采用正交设计试验研究了药典级DL -苹果酸的合成工艺。
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- 16. The pharmacopoeia, in other words, would create a set of standards that all parties could work towards.
- 换句话说，这部药典将建立一整套植物药材的标准。
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- 17. 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。
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- 18. No. The European Pharmacopoeia monographs are valid in all the Member States of the European Pharmacopoeia.
- 不需要。欧洲药典各论在欧洲药典所有成员国内均有效。
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- 19. According to synthesis and isolation of US patent, its purity cannot meet the requirement of pharmacopoeia.
- 由于美国专利合成与提纯方法过于简单且产率较低，纯度达不到医药级纯度。
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- 20. Results the physicochemical properties of the laboratory product met the requirement of American Pharmacopoeia.
- 结果实验室产品理化性能符合美国《药典》同类产品要求。
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- 21. In the case of a harmonised monograph, is it possible to use a reference standard from a different pharmacopoeia?
- 如果各论是协调过的，是否有可能使用不同药典的对照标准？
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- 22. The revised monograph for the new ORS formula will be published in the fourth edition of the International Pharmacopoeia.
- 修订的口服补液盐新配方专论将在国际药典第四版中发表。
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- 23. Methods By consulting Pharmacopoeia of China and Japanese Pharmacopoeia, the source of the crude drugs was compared.
- 方法通过查阅中国药典和日本药局方，比较生药来源。
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- 24. OBJECTIVE: to study the preparation techniques of ibuprofen tablet to meet the standard of Chinese pharmacopoeia 1995.
- 目的：探讨制备布洛芬片新的工艺条件，以达到中国药典1995年版新标准。
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- 25. Result: The phellem, phloem and xylem of wild bupleurum scorzonerifolium are different from those in the pharmacopoeia .
- 结果：野生狭叶柴胡的木栓层，韧皮部，木质部的显微特征均于药典上的记载有所不同。
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- 26. 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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- 27. 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。
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- 28. 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。
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- 29. 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。
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