PROTOCOL INFORMATION OFFICE (PIO) SUPPORT SERVICES FOR THE PROCESSING OF CLINICAL TRIAL PROTOCOL DOCUMENTS AND TRACKING THE IMPLEMENTATION AND COMPLETION OF HUMAN CLINICAL RESEARCH STUDIES. PERFORMANC

这一要求的主要目标是向NCI、DCP协议信息办公室(PIO)提供支持，这是由以下详细说明的五个项目领域定义的。 这五个项目范围是： 项目领域1.从与议定书有关的文件中提取关键要素 项目领域2.文件管理 项目领域3.临床试验评审支持 项目领域4.管理人员(如调查员、协调员、审查员。等)和组织在DCP临床试验数据库中的数据 项目领域5.PIO业务支持

The major objective of this requirement is to provide support, which is defined by the five project areas detailed below, to the NCI, DCP Protocol Information Office (PIO). The five project areas are: Project Area 1. Abstraction of Key Elements from Protocol Related Documents Project Area 2. File Management Project Area 3. Clinical Trial Review Support Project Area 4. Manage People (persons such as investigators, coordinators, reviewers. etc.) and Organization’s data in DCP Clinical Trials Database Project Area 5. PIO Operational Support