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Human Subjects Protection in the Era of the Revised Common Rule

机译:经修订共同规则时代的人类主体保护

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摘要

The last several years have been a time of significant change for the clinical research enterprise, not only at the national level with the revised regulations, but also at the local level with the growth and transitions in our own health system. As the current and former executive chairs of the Ochsner Institutional Review Board (IRB) system, we thank all of the authors and peer reviewers who made this special issue possible. Because of the revised federal IRB regulations (45 CFR §46, Subpart A) that became effective in January 2019, active review is underway at all US IRBs and human research protection programs about how the new regulations should be understood, implemented, and operationalized. We hope this special edition will assist many as they work through the various issues that have been raised by these changes. Highlights of this special edition issue include the following:
机译:对于临床研究企业而言,最近几年是一个重大变革的时期,不仅在国家一级修订了法规,而且在地方一级随着我们自身卫生系统的增长和过渡。作为Ochsner机构审查委员会(IRB)系统的现任和前任执行主席,我们感谢所有作者和同行审稿人使这一特殊问题成为可能。由于修订的联邦IRB法规(45 CFR§46,A部分)已于2019年1月生效,因此美国所有IRB和人类研究保护计划都在积极研究如何理解,实施和实施新法规。我们希望这个特别版能够为许多人提供帮助,帮助他们解决由这些更改引起的各种问题。本期特刊的重点包括:

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