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关键路径计划如何满足药品评价与研究中心的监管科学需求:一些示例说明。

How the Critical Path Initiative Addresses CDER's Regulatory Science Needs: Some Illustrative Examples.

作者信息

Geanacopoulos Mark, Barratt Ruth

机构信息

1 Center for Drug Evaluation and Research, Office of Translational Sciences, Food and Drug Administration, White Oak, Silver Spring, MD, USA.

出版信息

Ther Innov Regul Sci. 2015 Jul;49(4):466-472. doi: 10.1177/2168479014567323.

Abstract

Since 2008, the Critical Path Initiative has supported FDA's program of intramural research projects in regulatory science, with the goal of improving translation of advances in emerging sciences to the development of safe and effective medical products. Since 2011, the research of FDA's Center for Drug Evaluation and Research (CDER), including the work supported by the Critical Path Initiative, has been guided by the regulatory science needs identified in the CDER science and research needs report. In this review, the authors highlight a few of CDER'S Critical Path Initiative research projects, each addressing a different regulatory science need, to illustrate the diversity of regulatory science at CDER. They also describe elements common to these research projects, including broad collaboration with external partners, an increasing dependence on large data sets and computational models, and requirements for resources or perspectives specific to FDA.

摘要

自2008年以来,关键路径计划一直支持美国食品药品监督管理局(FDA)在监管科学方面的内部研究项目,目标是促进新兴科学进展转化为安全有效的医疗产品开发。自2011年以来,FDA药品评估和研究中心(CDER)的研究,包括关键路径计划支持的工作,一直以CDER科学与研究需求报告中确定的监管科学需求为导向。在本综述中,作者重点介绍了CDER关键路径计划的一些研究项目,每个项目都针对不同的监管科学需求,以说明CDER监管科学的多样性。他们还描述了这些研究项目共有的要素,包括与外部合作伙伴的广泛合作、对大数据集和计算模型的日益依赖,以及对FDA特定资源或观点的要求。

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