usp的例句大全

Information on Test Solutions ( TS) is provided in the Test Solutions portion of the Reagents, Indicators, and Solutions section of the USP – NF.

测试溶液（TS）的信息已在美国药典的试剂，指示物和溶液章节测试溶液部分中被提供。

Objective: To discuss the feasibility of using Chinese control standard endotoxin ( CSE) and Tachypleus Amoebocyte Lysate ( TAL) to substitute the USP Reference Standard Endotoxin ( RSE) and Limulus Amebocyte Lysate ( LAL) on the bacterial endotoxins test for streptomycin sulfate.

目的：探讨用中国的细菌内毒素工作标准品（CSE）和鲎试剂（TAL）替代美国的细菌内毒素参考标准品（RSE）和鲎试剂（LAL）来检测硫酸链霉素的细菌内毒素的可行性。

When water is called for in a compendial procedure, the USP article Purified Water shall be used unless otherwise specified.

制药过程中需要水的时候，除非有特殊情况，可以用USP文中的纯净水。

The free seminar is designed for the pharmaceutical and dietary supplement companies to learn the most recent information about USP standards and verification programs.

美国药典委员会也将派出多位专家为您讲解美国药典最新标准要求与认证资讯。

Sampled raw materials are tested in-country by the consulting firm using compendial USP and AOAC methods.

咨询公司按照美国药典要求，运用农业化学家协会的实验方法在中国国内对样品进行检测。

Suitability test for apparatus of USP dissolution test Research on the Environmental Suitability Test

对美国药典溶出度装置适用性试验的考察

Comparing the Examination Methods of Vegetable Drugs in USP with that in Chp

美国药典植物药检查方法与中国药典相关项目的比较

With the exception of one batch, all batches tested have met the USP XXII requirements for dissolution test in the case of the dissolution test.

在体外溶出实验中除一批外，其余各批均符合英国药典和USP XXII的溶出要求。

The quality control of the sodium alginate was already involved in the Pharmacopoeia of the United States ( USP) and British Pharmacopoeia ( BP).

对于海藻酸钠的质量控制标准，美国药典和英国药典等中已有规定，但我国药典中尚未收载。

Study of the statistical characteristics of the USP ⅹⅺ content uniformity sampling plan for tablets

美国药典ⅩⅪ版片剂含量均匀度检验方案的统计特性分析

Comparison of Content Uniformity Test between USP 29~ ( th) and ChP

美国药典29版与中国药典含量均匀度检查方法的比较分析

OBJECTIVE: To establish a method for the determination of taurine, and to compare which with that stated in Chinese Pharmacopoeia ( CP) and that stated in United States Pharmacopoeia ( USP).

目的：建立测定牛磺酸中主药及有关物质含量的方法，并与《中国药典》（药典）方法和《美国药典》（USP）方法比较。

Don't adopt a USP that you can't deliver, or further marketing is useless.

不要采用美国药典您不能发表，或其它的市场营销是没有用处的。

Use HPLC to experiment the different test in USP Pharmacopeia and Europe Pharmacopeia, and contrast the relationship of these results. 3.

采用高效液相法分析美国药典、欧洲药典中对大蒜项下大蒜辣素的检查，对比结果的相近程度和关系。

METHOD Base on determination of enzymatic active for papain in USP ⅹⅹⅲ. The analytical conditions were selected by orthogonal tests.

方法参照美国药典（USP）23版木瓜酶活力的测定方法，采用正交试验法对国内外测定条件进行了逐项试验的研究，筛选出最佳测定条件。

In this paper, The United States Pharmacopoeia ( USP) is introduced in terms of the history of publication, the constitution, the monograph and the future trend in the development.

本文对《美国药典》的出版历史、药典结构、收载品种特点以及以后的发展趋势等进行了较为详细的介绍。

The detected results were in agreement with the volumetric analysis in USP ( 23 ed.). It can be used instead of the volumetric method.

与美国药典（23版）上的规定的容量法相比较，所得分析结果相一致，可以代替容量法。

METHOD TLC Methods has been adopted in current edition of CP as well as in USP.

方法现版中国药典与美国药典均采用TLC法。

It has been used for the analysis of pethidine hydrochloride in tablet and dosage and the results agree with the USP method.

用此电极测定盐酸哌替啶针剂和片剂，取得了与美国药典标准方法相一致的结果。

Regulation of residual solvent in USP& from China-US joint symposium on pharmaceutical analytical technology and compendial methods

美国药典对残留溶剂的规定&写自第二届中美药品分析技术与检测方法研讨会