药品标准

  • 网络drug standard;drug specifications;GSP
药品标准药品标准
  1. 结果:新工艺制备的阿莫西林颗粒的含量、粒度、pH值均符合上述国家药品标准。

    Results : The content , particle size , and pH of amoxicillin granules prepared by the new process were in accordance with the criteria of National Drug standards .

  2. 目的:提高阿莫西林颗粒的质量稳定性,并符合国家药品标准[WS-10001-(HD-0102)-2002]规定。

    Aim : To improve the stability of amoxicillin granules and make it measure up to the criteria of National Drug Standards [ WS-1001 - ( HD-0102 ) - 2002 ] .

  3. PET放射性药品标准制订和质量控制初探

    Preliminary consideration on establishment of quality standards and quality control of radiopharmaceuticals for pet

  4. 本方法与国家药品标准的HPLC方法比较,所得结果基本一致。

    The results consisted with that of the HPLC method of the national drug standard .

  5. 药品标准中HPLC法色谱条件的优化与系统适用性试验的重要性

    The Optimum Chromatogram Conditions of HPLC and The Importance of System Suitability Method in Pharmaceutical Standard

  6. 结论修改后的TLC方法可用于《卫生部药品标准》中该品种薄层色谱鉴别。

    Conclusion The improved TLC method is suitable for the control of Jidesheng antivenomous tablets .

  7. 本文通过三例药品标准中的HPLC法试验,对HPLC法色谱条件的优化和系统适应性试验的重要性进行了讨论。

    The purpose of this paper is to evaluate a system suitability method and HPLC operating conditions by three pharmaceutical analysis studies .

  8. 目的:完善复方苯海拉明克罗米通酊的试行国家药品标准[1],增订乙醇量的GC测定法[2]和克罗米通含量的HPLC测定法,更好的控制产品质量。

    Objective : To develop a GC method for determination of ethanol and a HPLC method for assay for crotamiton to improve the current control method for Compound Diphenhydramine and Crotamiton Tincture and to control the product better .

  9. 在全自动化的生产过程中,严格执行ISO9001标准,按照国际最高药品标准EU-GMP的标准来控制生产流程。

    During the wholly-automatic producing progress , we strictly carries out ISO9001 standard and EU-GMP , the highest standard of international drugs .

  10. 脂溶性维生素注射液的细菌内毒素检查法,收载于卫生部药品标准中(1996年),其限值为L≤1Eu·ml~(-1)。

    The method of bacterial endotoxin test for liposoluble Vitamin injection has been developed in the Drug standard ( 1996 ) by Ministry of Health PRC .

  11. 在新药开发过程中,需要标定自己的药品标准物质。

    PRM should be determinated during new drug development and research .

  12. 结论:与卫生部药品标准(试行)中的方法相比,本法操作简便,分析结果更为准确。

    Conclusion : The method is simple , specific and accurate .

  13. 非水滴定在药品标准中的合理应用问题

    Application of titration in non-aqueous solvent in the control of pharmaceutical products

  14. 药品标准,食品卫生标准,兽药标准;

    Standards for pharmaceuticals , food hygiene and veterinary medicine ;

  15. 关于尽快建立我国药品标准中有关杂质命名规范的建议

    Suggestion on Establishing Standardization Nomenclature of Related Substance in National Drug Standards

  16. 新药开发研究过程中药品标准物质的标定

    The Determination of Pharmaceutical Reference Materials During New Drug Development and Research

  17. 浅析我国药品标准及其在新时期的地位与作用

    Discussion on Drug Specifications and Its Function in New Situation in China

  18. 其他不符合药品标准规定的。

    It fails in any other way to comply with stipulated drug standards .

  19. 从药品标准的使用率浅析现行药品标准存在的问题及对策

    Problems and Strategy on Current Drug Standards from the Usage Rate of Drug Standards

  20. 国家药品标准中值得注意的几个问题

    Several Noteworthy Problems in National Drug Standards

  21. 对菌体制剂药品标准的探讨

    The Discussion on Criteria of Fungi Medicaments

  22. 现有国家药品标准中复方制剂杂质控制的现状和思考

    Status and Perspective of the Impurity Control of Combination Preparations in Current National Drug Standards

  23. 药品标准查询系统设计

    Design of drugs standard inquiry system

  24. 国家药品标准中成药功能主治规范工作回顾与展望

    Review and Expectation of Task on Standardizing Indications of Traditional Chinese Medicines in National Drug Standards

  25. 药品标准与专利

    Pharmaceutical Standards and Patents

  26. 而新建立的两法简便、快速、准确,优于河北省药品标准法。

    The new methods are simple , rapid and accurate , and are better than Hebei pharmaceutical standard .

  27. 药品标准物质分包装工作是标准物质全部工作中重要的组成部分。

    The sub-packaging work of pharmaceutical standard material is an important part of the whole work of standard matter .

  28. 目的改进注射用赖氨匹林国家药品标准中含量测定方法。

    Aim To improve the method for assay of lysine acetylsalicylate for Injection on the drug specifications promulgated by the SFDA .

  29. 国际重磅药品标准演变分析及我国重磅药品标准探析

    The analysis on the regularity of standard development of Blockbuster Drugs in the world and on the standard of them in China

  30. 本法测定结果与黑龙江省药品标准方法测定结果基本一致。

    The results from the proposed method were in good accordance with those from the method given by drug standards in Heilongjiang Province .