Biorepository best practices for research and clinical investigations.

Biorepository best practices for research and clinical investigations.
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DOI:
10.1016/j.cct.2021.106572
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发表时间:
2022-05
影响因子:
2.2
通讯作者:
Schmelz, Monika
Schmelz, Monika
中科院分区:
医学4区
文献类型:
--
作者:
Sanderson-November, Micheline;Silver, Sylvia;Hooker, Vanessa;Schmelz, Monika

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转化研究需要高质量的标本来保证研究成果的完整性。临床研究不仅必须依赖于高质量的标本,而且还必须依赖于临床注释,以获得一致、准确和可验证的科学和临床结果。在由单个研究者对标本进行的实验室研究中,很容易保持质量控制。在多中心临床研究网络中,生物标本从采购到运输、处理、储存和最终检测的众多步骤需要严格标准化的操作工作流程和程序。中央生物储存库的做法可以为多中心临床研究提供信息,并有助于临床研究标本完整性的最佳实践。
Translational research requires good quality specimens to ensure the integrity of research results. Clinical research must rely not only on quality specimens, but as well on clinical annotation for consistent, accurate and verifiable scientific and clinical outcomes. In laboratory research performed on a specimen by a single investigator, quality control is easily maintained. In a multi-site clinical research network, the numerous steps for biospecimens from procurement through transport, processing, storage and ultimately testing requires strict standardization of operational workflows and procedures. The practices of a central biorepository can inform and contribute to best practices regarding clinical research specimen integrity for multi-site clinical research.
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