O'Neill R T
Office of Biostatistics, OTS/CDER/FDA, 10903 New Hampshire Avenue, Bldg 22, Room 6012, Silver Spring, MD 20993-0002, USA.
Biom J. 2006 Aug;48(4):559-64. doi: 10.1002/bimj.200510237.
This article describes the motivation for, description of, and the objectives and plans for the FDA's initiative that was introduced in March of 2004 by way of a report titled 'Innovation or Stagnation?--Challenge and Opportunity on the Critical Path to New Medical Products'. The FDA initiative is very much an outreach effort and a wake-up call to many constituencies to contribute and partner to improve the product development process and thereby to contribute to the success rate of new products that will benefit the public. We discuss in general terms where some of the opportunities and challenges exist for the discipline of biostatistics to make contributions to this effort over the next few years. In particular, guidance development in five areas is considered as is the need to devote new energy and efforts to quantitative risk assessment and safety evaluation, an area that has lagged the attention received in the efficacy evaluation area.
本文介绍了美国食品药品监督管理局(FDA)于2004年3月通过一份题为《创新还是停滞?——新医疗产品关键路径上的挑战与机遇》的报告所推出的一项举措的动机、描述以及目标和计划。FDA的这项举措在很大程度上是一项推广工作,也是对众多相关方的一次警钟,呼吁他们做出贡献并建立合作关系,以改进产品开发流程,从而提高将造福公众的新产品的成功率。我们大致讨论了生物统计学学科在未来几年为这项工作做出贡献时存在的一些机遇和挑战。特别是,我们考虑了五个领域的指南制定,以及投入新的精力和努力进行定量风险评估和安全性评价的必要性,而这一领域在关注度上一直落后于疗效评价领域。