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临床研究人员的财务披露——美国食品药品监督管理局。最终规则;对复议请愿书的行动。

Financial disclosure by clinical investigators--FDA. Final rule; action on petition for reconsideration.

出版信息

Fed Regist. 1998 Dec 31;63(251):72171-81.

Abstract

The Food and Drug Administration (FDA) is revising the requirements regarding financial disclosure by clinical investigators in order to add material to the codified language that was inadvertently omitted and to clarify the compliance dates to, in some cases, restrict the retroactive application of certain requirements of the rule. FDA is making these changes in order to respond to concerns raised by the Pharmaceutical Research Manufacturers Association (hereinafter referred to as "PhRMA"). By making these changes, FDA will be reducing the administrative burden for manufacturers and other affected parties while, at the same time, ensuring that the agency obtains the information that is most relevant to its review of clinical data submitted in marketing applications.

摘要

美国食品药品监督管理局(FDA)正在修订关于临床研究人员财务披露的要求,以便在编纂语言中补充无意中遗漏的内容,并在某些情况下明确合规日期,以限制该规则某些要求的追溯适用。FDA做出这些更改是为了回应制药研究和制造商协会(以下简称“PhRMA”)提出的担忧。通过做出这些更改,FDA将减轻制造商和其他受影响方的行政负担,同时确保该机构获得与其对上市申请中提交的临床数据审查最相关的信息。

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