MasoudMinimallyVaseiMinimallyMohammadMinimallyGhaneiMinimallyMostafaMinimallyEBSCO_AspArchives of Iranian MedicineVasei M, Ghanei M. Iranian registry of clinical trials: a four-year steady progress. Archives of Iranian medicine. 2013; 16(11):671....
BACKGROUND: Iranian Registry of Clinical Trials (IRCT) commenced its activities as a member of WHO registry network on fourth of December 2008. We explored the progress it has made within its first four years both in terms of quantity of registrations as well as its timeliness. MATHERIALS AND...
(11)日本临床试验注册中心 Japan Primary Registries Network (12)古巴临床试验注册中心 Cuban Public Registry of Clinical Trials (13)伊朗临床试验注册中心 Iranian Registry of Clinical Trials (14)非洲联盟临床试验注册中心 Pan African Clinical Trial Registry (15)斯里兰卡临床试验注册中心 Sri Lanka Clinical Trial...
如果两个被定义,设置P2优先权- USART0在USART1。 [translate] aA Song :Ican SayMy A B C 一首歌曲:Ican SayMy A B C [translate] aCLINICAL TRIALS REGISTRY 临床试验登记 [translate] 英语翻译 日语翻译 韩语翻译 德语翻译 法语翻译 俄语翻译 阿拉伯语翻译 西班牙语翻译 葡萄牙语翻译 意大利语翻译 荷兰语...
No abstract is available for this article.doi:10.1002/ibd.3780020409Lloyd R. SutherlandStephen B. HanauerJohn Wiley & Sons, Ltd.Inflammatory Bowel Diseases
The registration of clinical trials is an ethical responsibility and obligation for researchers. A clinical study is a public event itself, which needs the participation of the public, and its results should also be seen as a service to the public. Therefore, the public have the right to know...
Registry of prospective clinical trials second report 来自 Semantic Scholar 喜欢 0 阅读量: 17 作者: M Verstraete 摘要: PubMed comprises more than 23 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content ...
求翻译:registry and registration number for clinical trials是什么意思?待解决 悬赏分:1 - 离问题结束还有 registry and registration number for clinical trials问题补充:匿名 2013-05-23 12:21:38 正在翻译,请等待... 匿名 2013-05-23 12:23:18 书记官处为临床试验及注册号码 匿名 2013-05-23 ...
RS与临床研究(clinical trials)之间只有一个区别:RS是观察性的,而临床研究有更确定的患者或器械处置手段。在临床研究中,制造商指示研究人员以某种方式治疗该疾病。(将临床研究随机化后,它们称为随机临床研究或RCT。)换句话说,在RS中,医师按他们想要的条件进行治疗。在ULISSE RS,临床医生自主确定冠状动脉的再通方法。
Current development status of the World Health Organization's international clinical trials registry platform In 2012,Center for Drug Evaluation issued the "platform for registry and publicity of drug clinical trial".The preliminary research work focused on the thr... YZ Wang,XD Zhang,QZ Huang,.....