1)  Good Clinical Practice
临床试验规范
1.
Evidence-based Medicine and Principle of Good Clinical Practice in Clinical Research;
其实,临床研究规范(G oodClinical R esearch Practice)或临床试验规范(G oodClinical TrialPractice)比临床规范更为贴切。
2)  GCP audit
临床试验规范稽查
3)  clinical
临床
1.
Study on the clinical and pathologic tissue differentiation character of gastrointestinal stromal tumors;
胃肠道间质瘤临床与病理组织分化特性探讨
2.
The Clinical and X-ray Study of Tuberculosis of Lower Leaves;
下肺叶结核的临床及X线研究
3.
The expression of midkine factor and the clinical significance in different categories of pathology in cervical cancer;
MK因子在不同病理类型宫颈癌组织的表达及临床意义
4)  clinic
临床
1.
Clinical Analysis of 168 Cases with High Blood Pressure Merger the Apoplexy;
高血压合并脑出血168例临床分析
2.
Clinical analysis on treatment of chronic bronchitis;
慢性支气管炎临床治疗分析
3.
Research and practice of constructing lab teaching system of Chinese clinical medicine;
构建中医临床实验教学体系研究与实践
5)  pathology
临床
1.
Methods The data from 41 cases with ampulla cancer which had been diagnosed by operation and pathology,were analysised statistically.
目的　探讨壶腹部癌的临床病理特点 ,提高对壶腹部癌的临床诊治水平。
6)  clinical practice
临床
1.
Emphasizing training of basic skills and improving students ability in clinical practice;
注重基本技能训练 提高学生临床实践能力
2.
Analysis of Some Problems in the Clinical Practice of Making TCM Formulas;
对方剂配伍临床研究中几个问题的探析
参考词条
补充资料：临床试验
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CAS号：

性质：新药的临床试验一般分三期或四期进行。多数国家按四期进行。工期临床试验(phase工Clinical trials)是在人体进行新药试验的起始期。包括药物耐受性(toierance)试验与药代动力学(pharmacokinetics)，生物利用度(bioavailability)研究。Ⅱ期临床试验(phaseⅡ clinicaltrials)要对新药的疗效、适应症、不良反应进行详细考察。通过随机对照临床试验对新药的安全有效性作出确切评价。III期临床试验(phase III clinical trials)为扩大临床试验，目的是在较大范围内对新药的疗效、适应症、不良反应、药物相互作用等进行评价。Ⅳ临床试验(phase IV clinical trials)是在新药投产后进行的，为上市后临床试验或称为上市后药物监察(postmarketing surveillance)。目的是对已在临床广泛应用的新药进行社会性考察，着重于新药的不良反应监察(ad-Verse drug reaction surveillance)。

说明：补充资料仅用于学习参考，请勿用于其它任何用途。