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Investigating the Food and Drug Administration (FDA) Biotherapeutics Review and Approval Process: A Scoping Review

机译:调查食品和药物管理局(FDA)生物治疗药物的审查和批准过程:范围审查

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Suggesting changes to the review and approval of therapeuticbiological products is a challenging task. To the best ofour knowledge, none of the academic articles identified in thisscoping review have modeled the FDA review and approvalprocess to address issues related to the robustness, reliabilityand efficiency of its operations from an internal point of view.The reform models identified in the literature are limited in severalaspects. For example, there is a general lack of applicationof scientific methodologies and modeling techniques in understandingFDA as a complex sociotechnical system. In addition,tools and methods to assess their efficacy before implementationare largely absent.
机译:建议更改治疗的审查和批准 生物产品是一项具有挑战性的任务。尽力而为 我们的知识,在此未找到任何学术文章 范围审查已对FDA审查和批准进行了建模 解决与鲁棒性,可靠性有关的问题的过程 从内部角度来看其运作效率。 文献中确定的改革模式仅限于以下几种 方面。例如,普遍缺少应用程序 科学方法论和建模技术的理解 FDA是一个复杂的社会技术系统。此外, 在实施前评估其效力的工具和方法 基本上不存在。

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