Federal Electronic Adverse Event Reporting System in the Works

Emily Ethridge

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Federal Electronic Adverse Event Reporting System in the Works

机译：工程中的联邦电子不良事件报告系统

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The FDA and the NIH are aiming to make it easier for the public to report adverse events by collaborating on a way to electronically submit them in a range of forms federal agencies already use. The agencies signed a memorandum of understanding (MOU) to create a web-based method for consumers, healthcare professionals, sponsors and other parties to submit adverse event reports, according to a notice to be published in the Feb. 6 Federal Register.

机译：FDA和NIH的目的是通过合作以电子方式以联邦机构已经使用的多种形式提交不良事件的方式，使公众更容易报告不良事件。根据将于2月6日发布的公告，该机构签署了一项谅解备忘录（MOU），以创建一种基于网络的方法，供消费者，医疗保健专业人员，赞助商和其他各方提交不良事件报告。

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《Washington Drug Letter》 |2008年第6期|p.5|共1页
作者
Emily Ethridge;
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正文语种 eng
中图分类生物科学;
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Federal Electronic Adverse Event Reporting System in the Works

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