• 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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  • Conclusion Sterility test medium manufacturers should be put in production license system.

    结论应实行无菌试验培养基生产企业生产许可证制度。

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  • Objective To discuss the current situation of drug sterility test in our country.

    目的讨论目前我国药品无菌试验实际情况

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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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  • 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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  • 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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  • 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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  • 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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  • 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 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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  • Methods The sterility test technology was applied after dry heat sterilization.

    方法干热灭菌,用无菌检测技术检测。

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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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  • 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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  • The following culture media have been found to be suitable for the test for sterility.

    下面培养基已经证实适合进行无菌检查

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

    无菌检测试验无菌条件下进行

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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 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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  • In the case of validation, recovery, toxicity of the dilution medium and sterility (negative test) are examined to guarantee the suitability of the test in the presence of the product.

    如果需要确认恢复,就要检测稀释培养基毒性无菌性(阴性测试)确保测试适用于现存药品。

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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 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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  • 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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  • 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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  • 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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  • 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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