临床试验,clinical trial
1)clinical trial临床试验
1.EMEA"s consideration on strategy and design ofclinical trials for new antibacterial agent;欧盟医药管理局对新抗菌药物临床试验策略和设计的考虑
2.FDA"s general considerations on the antibacterial dugsclinical trial protocol issues and its enlightenment;美国FDA对抗菌药物临床试验方案的考虑及其借鉴
3.FDA"s considerations of non-inferiority design used in anti-bacterial drugclinical trials;美国FDA对抗菌药物临床试验非劣效设计的考虑
英文短句/例句
1.Inverting Onus of Proof Try Clinical Test;“举证责任倒置”对临床试验的考验
2.Research and Clinical Experiment of the Ashma Easing Effect of Lumbricin9201;蚯蚓素_(9201)平喘的实验研究和临床试验
3.Work experience of clinical research coordinator in clinical trials of new drugs在新药临床试验中开展临床研究协调员工作
4.Important role of drug clinical trial institution in quality assurance system药物临床试验机构在药物临床试验质量保证体系中的重要作用
5.Sample Size and Power Determination for Interval Test in Clinical Trial;临床试验中区间检验的样本量与检验效能估计
6.Therapentic Misconception and Countermeasures in Clinical Research论临床试验中的治疗性误解及对策
7.Experimental study of optimization for formulation of Fukang balm肤康涂膜剂处方优选的临床试验研究
8.Exploitation and Application of Clinical Trial Dat Management System;临床试验数据管理软件的开发与应用
9.Analysis on Implementation of Good Clinical Practice Guidelines in Vaccine Trial;GCP原则在疫苗临床试验中的实施分析
10.Analysis of Conflicts of Interest in Gene Therapy Clinical Trials;浅析基因治疗临床试验中的“利益冲突”
11.Clinical Study on Chinese Herb Antivirus of Preventing and Treating Avian Influenza;中药“病毒清”防治禽流感病的临床试验
12.Studies on GCP and Supervision for Drug Clinical Trials in China我国GCP与药物临床试验监管研究
13.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
14.Construction and Management of Drug Clinical Trial Institution in Our Hospital我院药物临床试验机构的建设和管理
15.A Clinical Study on Oxiracetam Capsule for Dementia Therapy奥拉西坦胶囊治疗痴呆临床试验研究
16.APPLICATION OF PROPENSITY SCORE IN NON-RANDOMIZED CLINICAL TRIAL非随机化临床试验中倾向指数的应用
17.A phase II clinical trial of morphine sulfate suppository in the treatment of cancer pain硫酸吗啡栓治疗癌痛的Ⅱ期临床试验
18.Preclinical and Phase Ⅰ Clinical Trials of Salvicine;沙尔威辛临床前试验及Ⅰ期临床研究
相关短句/例句
clinical trials临床试验
1.Several Points in Ethic Review in Drug Clinical Trials;药物临床试验的伦理审查几个要点
2.Simulations of urn model and RPW rule of adaptive design inclinical trials;临床试验中自适应设计的urn模型和RPW规则及其模拟
3.Main points of design about phase I tolerantclinical trials of injectable preparation;注射剂I期耐受性临床试验方案设计要点
3)clinical trail临床试验
1.Hospital ethnic committee construction andclinical trail ethic audit;医院伦理委员会的建设与临床试验的伦理审核
2.On Some Issues in Pediatric Clinical Trails儿童临床试验若干问题的体会
3.Inspection of ethical issues in multicenterclinical trails in China:a survey of current status中国大陆部分多中心临床试验伦理审查模式现状调查
4)clinical test临床试验
1.Method Theclinical test of multicentric random parallel control was used.方法多中心随机平行对照临床试验。
2.Methods:Through the relevant exprinents and analysis of documental materials, by summarizing the information about the source of ursolic acid and its feature of physics and chemistry, through identification and measure of its structure and content by analysis of its pharmacological functions and byclinical tests and studies on the productive technology.方法:通过有关试验研究和文献资料的调研分析,综述近年来有关乌索酸的资源情况、理化性质、结构鉴定、含量测定、药理作用、临床试验以及生产工艺方面的研究状况。
5)clinical trails临床试验
1.Objective index for evaluating cerebral atherosclerosis inclinical trails;脑动脉硬化药物临床试验客观指标探讨
2.Issues ofclinical trails on traditional Chinese new drugs for diabetic polyneuropathy;糖尿病周围神经病变中药临床试验中的几个问题
3.Some problems onclinical trails evalution of herbs medicine for insomnia;失眠症中药新药临床试验疗效评价的几个问题探讨
6)clinic trial临床试验
延伸阅读
临床试验分子式：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)。
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