• A sterility test method for the Compound Sulfadiazine Zinc Cream was established.

    建立复方磺胺嘧啶乳膏无菌检查法

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  • Conclusion The sterility test reassured by verification test is feasible and reliable.

    方法采用直接接种法,通过无菌验证试验确定无菌检查方法的有效性。

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  • Conclusion: The established sterility test method for Imipenem monohydrate may be practical.

    结论建立亚胺培南一水合物无菌检查法可供实用。

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  • Conclusion the established sterility test method of the Burn I oil agent is scientific and accurate.

    结论采用该法烧伤一号油剂进行无菌检查方法可行,结果准确

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  • They are widely used for gravimetric analysis, microanalysis, colloid separation and sterility test.

    广泛用于重量分析微量分析胶体分离无菌实验中

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  • Conclusion: This method is accurate, it can be used for sterility test of Oxaliplatin for Injection.

    结论注射奥沙利无菌检查通过验证

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  • Objective To establish a methods for determining sterility test of Cefonicidum Natricum for Injection.

    目的建立注射用头孢尼西无菌检查方法

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  • Objective To establish and verify the sterility test method for Ginseng and Prepared Aconite Injection.

    目的建立附注射液无菌检查方法进行验证

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  • Leading sterilization team on sterilization daily work, Microbiology lab routine work and sterility test.

    领导灭菌团队日常工作微生物实验室无菌测试管理。

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  • 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

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  • Conclusion: The method is accurate and reliable. It can be used for sterility test of Xingnaojing injection.

    结论:经方法学验证,醒静注射液无菌检查法准确可靠

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  • Methods: The validation for sterility test includes inhibition test for bacteria and fungi and irrigation test.

    方法无菌检查法验证试验——细菌抑真菌试验冲洗量试验。

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  • Objective:To determine the validity of membrane filtration method in the sterility test of little capacity injection.

    目的探讨薄膜过滤容量注射剂无菌检查中应用可行性

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  • Objective:The suitable method was selected for the sterility tests of Imipenem Monohydrate to guarantee the test result accurate and reliable.

    前言: 目的:选择亚胺培南一水合物无菌检查适宜检查方法保证检验结果准确性可靠性。

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  • Objective:To verify soybean-casein digest medium in USP whether or not substitute fungi medium in Pharmacopeia of P. R. China(ChP)by sterility test.

    前言: 目的:验证美国药典大豆- 酪蛋白消化培养基能否替代中国药典无菌检查用真菌培养基。

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  • The microorganism which discovered in the production environment should take regularly uses in the sterility test method confirmation the challenge mold mushroom spawn;

    生产环境发现微生物定期地作为用于无菌检查方法验证的挑战菌种;

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  • Methods Sterility test, mycoplasma detection, pyrogen detection and abnormal toxicity test were performed respectively on culture supernatant of neural stem cells from bone marrow.

    方法骨髓源性神经干细胞的培养上清分别进行无菌试验支原体检测热原质检测异常毒性试验。

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  • The isolation system shall be validated according to the relevant requirements, and the cleanliness of the internal environment shall comply with the requirements of the sterility test.

    隔离系统相关要求进行验证内部环境洁净度符合无菌检查的要求。

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  • As to be the drag manufacturer, it will directly influence the biological quality control of sterility product that the contaminations control during injection production and sterility test.

    作为药品生产单位,无菌注射剂生产污染控制无菌检查直接影响到无菌产品微生物方面的质量控制。

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  • The test for sterility is carried out under aseptic conditions. In order to achieve such conditions, the test environment has to be adapted to the way in which the sterility test is performed.

    无菌检查无菌条件进行为了达到条件,检测环境符合无菌检查的规定。

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  • If no evidence of microbial growth is found in the repeat test, the product examined complies with the test for sterility.

    如果复检中发现微生物生长证据,则该供试产品符合无菌试验的要求。

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  • If microbial growth is found in the repeat test, the product examined does not comply with the test for sterility.

    如果复检中发现微生物生长,则产品符合无菌试验

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  • The test for sterility may then be carried out without further modification.

    然后无菌试验可以进行而无需进一步变更

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  • Carry out a test as described below under test for Sterility of the Product to be Examined using exactly the same methods, except for the following modifications.

    按照下面供试产品无菌检查项描述使用除了下面变更之外完全相同方法进行试验

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  • If no evidence of microbial growth is found, the product to be examined complies with the test for sterility.

    如果没有找到微生物生长证据,则该供试产品符合无菌检查

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  • If the membrane filtration technique is unsuitable, use the Direct Inoculation of the Culture Medium method under Test for Sterility of the Product to be Examined.

    如果过滤技术适合,则使用在供试产品无菌检查法培养基直接接种

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  • The validated method can be used to test for sterility of Cefpirome Sulfate for Injection.

    采用验证试验方法进行注射用硫酸头孢匹罗无菌检查可行

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  • A test method for sterility of Levofloxacin Hydrochloride and Sodium chloride Injection was established.

    建立盐酸氧氟沙星氯化钠注射液无菌检查方法

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  • Pharmacopeial articles are to be tested by the Membrane Filtration method under test for Sterility of the product to be Examined where the nature of the product permits.

    只要其性质许可,这些药品使用供试产品无菌检查法项过滤检测

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  • The test for sterility is carried out under aseptic conditions.

    无菌检查无菌条件下进行

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