Clinical Protocol and Data Management (Core-013)

临床方案和数据管理（Core-013）

• 批准号: 9071747
• 负责人: miriam bischoff
• 金额: $ 48.98万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-06-04 至 2021-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9071747
• 关键词: Awareness; Clinical; Clinical Data; Clinical Protocols; Clinical Research; Clinical Trials; Communities; Conduct Clinical Trials; Data Collection; Documentation; Good Clinical Practice; Institutes; Malignant Neoplasms; Medical Research; National Clinical Trials Network; Patient Care; Performance; Procedures; Process; Protocols documentation; Reporting; Research; Research Personnel; Resources; Services; Translational Research; anticancer research; cancer clinical trial; cancer education; data management; design; improved; interdisciplinary collaboration; outreach; programs; quality assurance; systems research

PROJECT SUMMARY CLINICAL PROTOCOL & DATA MANAGEMENT The Clinical Protocol and Data Management Office, known at Stanford as the Cancer Clinical Trials Office (CCTO), provides a centralized resource that assists clinical researchers with regulatory, financial, study conduct, and administrative services in order to facilitate efficient activation and conduct of protocols, thus allowing the researcher to focus on scientific research needs and patient care. CCTO programs are designed to increase awareness of and accrual to clinical trials, as well as to centralize and standardize the processes, quality and efficiencies of conducting clinical trials in compliance with the regulatory, documentation, and oversight requirements. The CCTO has developed and employs standard processes for clinical trial conduct in line with Good Clinical Practice and National Clinical Trials Network (NCTN) operational requirements. The CCTO continually reviews processes searching for ways to improve procedures and services, as well as to enable the highest quality conduct of SCI's clinical research.

项目摘要 临床方案和数据管理 临床方案和数据管理办公室，在斯坦福大学被称为癌症临床试验办公室 （CTO），提供一个集中的资源，协助临床研究人员进行监管，财务，研究 行为和行政服务，以促进有效激活和执行协议，从而 使研究人员能够专注于科学研究需求和患者护理。CTO计划包括 旨在提高对临床试验的认识和收益，以及集中和标准化 按照监管要求开展临床试验的流程、质量和效率， 文件和监督要求。CTO已开发并采用标准流程 根据药物临床试验质量管理规范和国家临床试验网络（NCTN）开展临床试验 业务要求。CTO不断审查流程，寻找改进方法 程序和服务，以及使SCI的临床研究的最高质量的行为。