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

	University of New Mexico School of Engineering MINOR PARTICIPANT WAIVER AND NOTICE OF RISK Activity Title UNM SOE High School Research Learning Experiences DocID: 1vbV0 - View Document
	eInterview.org Consent Form Participant Copy This study involves a web-based interview about various lifestyle attitudes and behaviors. The interview is not for commercial purposes; it is part of a research project being DocID: 1uQc5 - View Document
	To: Tetsuro Matsuzawa Program Coordinator, Leading Graduate Program in Primatology and Wildlife Science Professor, Primate Research Institute Overseas Research Participant Pledge（For International Students） I hereby DocID: 1uDiF - View Document
	Participant Handbook This project is funded by the USFWS Competitive State Wildlife Grant Program and the Foundation for Food and Agricultural Research Cover photo: Bombus vosnesenskii on Arrowleaf Balsomroot. Photo by DocID: 1tXQr - View Document
	PI: Mark A. Supiano, MD Center on Aging Research Participant Registry Version 2.0 July 12, 2010 Page 1 of 6 DocID: 1tOn5 - View Document