Clinical Agent and Specimen Repository

临床制剂和样本库

• 批准号: 8870231
• 负责人: JOHN KUDRICK
• 金额: $ 303.05万
• 依托单位: FISHER BIOSERVICES, INC.
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-22 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8870231
• 关键词: Clinical; Clinical Research; Clinical Trials; Contracts; Good Clinical Practice; Shipping; Ships; Specimen; good laboratory practice; programs; repository

The Clinical Agent and Specimen Repository contract adheres to current Good Manufacturing Practice (cGMP), Good Clinical Practice (GCP), and Good Laboratory Practice (GLP) for the acquisition, receipt, storage and shipping of clinical agents and clinical specimens in support of DMID-sponsored clinical trials and research programs in the U.S. and abroad.

临床试剂和标本储存库合同遵守当前的良好制造规范(CGMP)、良好临床规范(GCP)和良好实验室规范(GLP)，用于购买、接收、储存和运输临床试剂和临床标本，以支持DMID赞助的美国和海外的临床试验和研究计划。