double-blind, clinical trial of the effect of modafinil on cancer-related fatigue among 631 patients receiving chemotherapy: a university of rochester cancer center community clinical oncology program research base study[J]. Cancer, ...
Clinical Trial/Study Report 临床试验/研究报告 A written description of a trial/study of any therapeutic, prophylactic, or diagnostic agent conducted in human subjects, in which the clinical and statistical description, presentations, and analyses are fully integrated into a single report (see the ICH...
个人理解:支持,无异议。 http://weixin.qq.com/r/TRG0rLXE5eiarfHP90Rf (二维码自动识别) Tips:最近想看临床试验各岗位机会要内推的小伙伴可以添加公众号(临床试验达人)私信或微信(ClinicalTrial888)~优质岗位等你来选~ 编辑于 2022-11-03 15:29・IP 属地上海 ...
• Clinical trial application ,CTA 临床试验申请 • Clinical trial exemption ,CTX 临床试验免责 • Clinical trial protocol ,CTP 临床试验方案 • Clinical trial/study report 临床试验报告 • COA(药品检测报告) • Co-investigator 合作研究者 • Comparison 对照...
Electronic Case Report Form (eCRF): An auditable electronic record designed to record information required by the clinical trial protocol to be reported to the sponsor on each trial subject. 电子病例报告表:可审计的电子记录,旨在记录临床试验方案要求向申办方报告的每个受试者的信息 ...
本文基于经历的几项国内外眼科临床试验研究,结合眼科医学,查阅相关文献以及参阅ClinicalTrial.gov公开的相关眼科临床试验,聚焦眼科临床研究常见的疾病领域,例如年龄相关性黄斑变性(AMD)、糖尿病性视网膜病变(DR)、糖尿病性黄斑水肿(DME)、干眼、小儿近视等,分享几点我在眼科临床试验研究CRF设计中的几点思考。
CRFs are used to collect data from patients during clinical trials. CRF design has a direct impact on the success of clinical trial data as it helps to evaluate the effectiveness of the medical product being trialled. Well-designed CRFs assist with data analysis and reporting, data management...
BUTLER J M Jr, CASE L D, ATKINS J, et al. A phase Ⅲ, double-blind, placebo-controlled prospective randomized clinical trial of d-threo-methylphenidate HCl in brain tumor patients receiving radiation therapy[J]. Int J Radiat Oncol Biol Phys, 2007, 69(5): 1496-1501. ...
Gilbert Hunter, Customer Success Manager at Certara, leverages over a decade of experience in technical writing, professional services, and CDISC-based training to help organizations enhance clinical trial design and regulatory submissions. His focus is on enabling customers to overcome challenges and ach...
In Oracle Clinical and RDC Classic, the term "CRF", which is an acronym for Case Report Form, refers to the form that is used by investigators to collect information and data about a patient in the clinical trial. This form can be either paper or electronic.In...