The Networked IRB Database

网络IRB数据库：该提案是达特茅斯学院和费城儿童医院的联合开发。该提案的长期目标是建立一个全国性的、集中的、安全的基于网络的IRB数据库，具体目标是在IRB、研究人员和申办者之间提供一种有效和高效的教育和沟通手段。该数据库将协调IRB的活动，并允许批准多个机构使用的方案和同意书。在参与多中心研究时，它也将是协调多个IRB活动的系统。 网络IRB数据库将通过三个独特的模块促进教育、标准化和交流： A.研究方案和知情同意书开发模块 B。研究方案和知情同意书分发模块以及 C.网络IRB审查数据库模块 每个模块都需要一个开发阶段和一个长期维护计划。 “网络IRB”系统将是全国现有（或计划的）当地IRB电子管理系统的附加组件。这个全国性的集中数据库将与地方系统连接，并将协助参与人类受试者研究的多个组成部分。教育、标准化和沟通的加强将对整个研究界产生重大影响，包括IRB、研究人员和赞助商。

The Networked IRB Database : This proposal is the joint development of Dartmouth College and the Children's Hospital of Philadelphia. The long term objective of this proposal is the establishment of a national, centralized and secure web-based IRB database, with the specific aim of making possible an effective and efficient means of education and communication among IRBs, researchers, and sponsors. The database will coordinate the activities of IRBs and allow for the approval of protocols and consent forms used in multiple institutions. It will also be a syslem for coordinating activities of multiple IRBs when participating in multi-center research studies. The Networked IRB Database will promote education, standardization and communication via three unique modules: A. Research Protocol and Consent Development Module B. Research Protocol and Consent Distribution Module and C. Networked IRB Review Database Module Each module will require a development phase, and a long term maintenance plan. The "Networked IRB" system will be an add-on to existing (or planned) local IRB electronic management systems throughout the country. This national, centralized database will interface with local systems and will assist nmltiple constituents involved in research with human subjects. The enhancement of education, standardization, and communication will have a significant impact on the entire research community including IRBs, researchers, and sponsors.