DE PEDIATRIC COBRE: CLINICAL RESEARCH SERVICES CORE

DE PEDIATRIC COBRE：临床研究服务核心

• 批准号: 8168439
• 负责人: Thomas H Shaffer
• 金额: $ 7.44万
• 依托单位: ALFRED I. DU PONT HOSP FOR CHILDREN
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-17 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8168439
• 关键词: Childhood; Clinical Pharmacology; Clinical Research; Clinical Trials; Computer Retrieval of Information on Scientific Projects Database; Consent; Data Base Management; Ensure; Funding; Grant; Human Subject Research; Institution; Research; Research Design; Research Ethics Committees; Research Personnel; Resources; Services; Source; Training; Translational Research; United States National Institutes of Health; Work; human subject; meetings; programs; protocol development; research study

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The Clinical Research Services Core will enhance the services that the existing Clinical Pharmacology Program provides for studies involving human research subject. This program currently provides oversight and facilitation of clinical trials; this does not fulfill the needs of the basic and translational research proposed in this Center application. We will expand the services of this core to directly serve the needs of research studies involving human subjects. The core will provide trained study coordinators who will assist the target investigators with study design, subject recruitment and database management, as well as facilitate interactions with the IRB by working with the target investigators on protocol development and consent to ensure that they meet institutional and federal requirements.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 临床研究服务核心将加强现有临床药理学项目为涉及人类研究受试者的研究提供的服务。 该计划目前提供临床试验的监督和促进;这不满足本中心申请中提出的基础和转化研究的需求。 我们将扩大该中心的服务，以直接满足涉及人类受试者的研究需求。 核心将提供经过培训的研究协调员，他们将协助目标研究者进行研究设计、受试者招募和数据库管理，并通过与目标研究者就方案制定和知情同意进行合作，促进与IRB的互动，以确保其符合机构和联邦要求。