CLINICAL TRIALS

临床试验办公室 MCC临床试验办公室（CTO）为临床试验的各个方面提供全方位的研究服务。 该中心的研究计划中的试验。这包括方案制定和准备， 法规遵从性、质量保证、数据和安全性监测、研究护理和研究 管理它分为三个部门，报告CTO主任，Joanne Mortimer，MD：研究 设计和开发、运营（包括法规事务、研究管理和研究）。 运营）以及社区和附属机构联络。CTO解决了临床科学家的需求， 制定和激活协议，并作为医疗保健团队的一个组成部分， 为协议患者提供最先进和有效的临床护理。CTO经历了 在过去的赠款期间进行了相当大的重组，数据质量不断提高， 累积到治疗试验。由于这些变化，1KB批准和签约所需的时间 数据采集的质量有所提高。这些改进有助于 患者应计费用的增加。

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.