CLINICAL TRIALS

临床试验办公室 MCC临床试验办公室(CTO)为临床研究的各个方面提供全方位的研究服务 在该中心的研究项目中进行试验。这包括协议的制定和准备， 法规遵从性、质量保证、数据和安全监控、研究护理和研究 管理层。它被组织成三个部门，报告首席技术官主任，医学博士乔安妮·莫蒂默：研究 设计与开发、运营(包括法规事务、学习管理和研究)。 业务)以及社区和从属关系联络。首席技术官解决了临床医生科学家在 方案的制定和激活，也是#年卫生保健团队不可或缺的一部分 为礼仪患者提供最先进和高效的临床护理。首席技术官经历了 在过去赠款期间进行了相当大的重组，数据质量和 应计入治疗试验。作为更改的结果，1KB审批和签约所需的时间 显著减少，数据捕获质量有所提高。这些改进做出了贡献 增加了病人的收入。

Clinical Trials Office The MCC Clinical Trials Office (CTO) provides a full range of research services for all aspects of clinical trials in the Research Programs of the Center. This includes protocol development and preparation, regulatory compliance, quality assurance, data and safety monitoring, research nursing, and study management. It is organized into three divisions, reporting the CTO director, Joanne Mortimer, MD: Study Design and Development, Operations (including Regulatory Affairs, Study Administration and Study. Operations) and Community and Affiliations Liaison. The CTO addresses the needs of clinician scientists in the development and activation of protocols and also functions as an integral part of the health care team in providing state of the art and efficient clinical care to the protocol patient. The CTO has undergone considerable reorganization during the past grant period, with increasing improvement in data quality and accrual to therapeutic trials. As a result of changes, the time required for 1KB approval and contracting has decreased significantly and the quality of data capture has improved. Such improvements have contributed to an increase in patient accruals.