grain certification

The hardware composition of the grain pest detection system was introduced.

介绍了谷物害虫检测系统的硬件组成,描述了采用差分图像法实现对谷物害虫检测判断和三帧差分法实现谷物害虫 图像恢复与提取的方法,最后利用图像的一阶灰度值直方图和图像的目标区域,自动提取静态仓储物害虫图像的纹理等特征, 实现对仓储物害虫的快速鉴定和分类。

Application of SPMEE in misued drug inspection;

固相微萃取膜(SPMEE)在滥用药物检验中的应用

Summary of analysis methods of benzodiazepines in biological samples;

生物样品中苯二氮卓类药物检验概述

A medical examiner found that the death was accidental cause (caused) by a mixture of medicines.

一个药物检验员发现死因是混和服用多种药物。

safer methods of testing drugs

检验药物的更可靠的方法

Brief talk on main points of on-site inspection of drug clinical trial institutions

浅谈药物临床试验机构现场检查要点

Effect of Some Drugs on Common Clinical Biochemistry Tests;

部分药物对常用临床生物化学检验项目的影响

Preliminary study on the appropriate concentrations of drug used in the drug-susceptibility test to detect the Ethambutol-resistant isolates of Mycobacterium tuberculosis

比例法药敏试验检测乙胺丁醇耐药适合药物浓度的初步探讨

Evaluation of Sensitivity of Antitumor Drugs in Human Bladder Cancer by MTT Assay in Vitro;

MTT法检测人膀胱癌体外药物敏感性实验研究

Study on Influencing Factors of the Industrialization for Bio-pharmaceutical Enterprises: An Empirical Study;

生物制药产业化的影响因素研究:一个实证检验

DETERMINATION OF DIPHACINONE AND BRODIFACOUM IN BIOLOGICAL SAMPLES;

生物样品中敌鼠钠盐和溴敌隆杀鼠药的检验

Examination of bacterial pathogens isolated from the leech,Hirudinaria manillensis Lesson,1842 and medication therapy

菲牛蛭细菌性疾病的病原检验及药物防治

Types and main points of site inspections of drug clinical trial institutions in China

我国药物临床试验机构现场检查的类型和要点

MICROBIAL LIMIT TESTS FOR THREE CHINESE DRUG PREPARATIONS

三种中药制剂微生物限度检查方法验证

Verification on the Detection of Hormone Medicine Residues in the Factory Environments

生产环境中激素类药物残留量检测验证

Expert Group on the Detection and Assay of Controlled Drugs in Biological Specimens

检验和化验生物标本中含有的受管制药物问题专家组

Qualitative or quantitative analysis of a substance, especially of an ore or drug, to determine its components.

化验，分析物质的定性或定量分析，尤指矿石或药物，检验内含成份

The Food and Drug Administration says the results should be confirmed by other tests.

食物与药品管理局说检验结果须经其它检查证实。

Discussing the validation tests for time of adding the tested microorganisms in the microbial limit test described in ChP 2005

2005年版中国药典微生物限度检查法验证试验中加菌时间的探讨

For the re-inspection on biological products, an applicant may directly file an application to the National Institute for the Control of Pharmaceutical and Biological Products.

生物制品的复验直接向中国药品生物制品检定所申请。