Data and Safety Monitoring System

ID Simon癌症中心的数据和安全监测功能是主要的 临床试验监查委员会（CTMC）的职责。其功能与 科学审查委员会，该委员会评估所有癌症相关临床研究的科学价值， 中心的审判。 IUSCC临床试验监测委员会（CTMC）由Romnee Clark博士担任主席。的 CTMC的主要职责是评估试验特定数据安全性的充分性 SRC审查的每个方案的监测计划（DMSP），以审查ILJSCC赞助的 患者安全性研究，以确保方案和不良事件报告的依从性，并进行 内部审计和质量保证审查。 临床研究委员会（CRC）由Kathy米勒博士担任主席，他是 临床研究，监督SRC和CTMC的政策和程序，每月收到 报告这些委员会的活动，并在发生争议时进行仲裁。

The Data and Safety Monitoring function of the ID Simon Cancer Center is the primary responsibility of the Clinical Trials Monitoring Committee (CTMC). Its function is closely related to the Scientific Review Committee, which evaluates the scientific merit of all cancer-related clinical trials of the Center. The IUSCC Clinical Trials Monitoring Committee (CTMC) is chaired by Dr. Romnee Clark. The primary responsibilities of the CTMC are to assess the adequacy of trial-specific data safety monitoring plans (DMSP's) for each protocol reviewed by the SRC, to review ILJSCC-sponsored studies for patient safety, to ensure protocol and adverse event report compliance, and to conduct internal audits and quality assurance reviews. The Clinical Research Committee (CRC) chaired by Dr. Kathy Miller, Interim Associate Director for Clinical Research, oversees the policies and procedures of the SRC and CTMC, receives monthly reports of the activities of these committees, and arbitrates in the event of disputes.