Stanford University IRB Guidance

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Date: 2016-04-12 01:21:51 Medical ethics Clinical research Human subject research Design of experiments Informed consent Clinical trial Consent Research participant Placebo-controlled study Food and Drug Administration Clinical research coordinator Institutional review board		Stanford University IRB Guidance Add to Reading List Source URL: humansubjects.stanford.edu Download Document from Source Website File Size: 49,96 KB Share Document on Facebook

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	From the Consent of the Routed: Improving the Transparency of the RPKI Full version from June 9, 2014. Ethan Heilman Danny Cooper Leonid Reyzin DocID: 1xU8V - View Document
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