Stanford University IRB Guidance

First Page		Document Content
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

	Microsoft Word - SOP - IRB Membership.docx DocID: 1rrOd - View Document
	FIERC Form 2.2 Requirement Checklist Food and Nutrition Research Institute Ethics Review Committee DocID: 1rp40 - View Document
	DOC Document DocID: 1rnQe - View Document
	Westminster College Institutional Review Board (IRB) For the Protection of Human Subjects DocID: 1rm2u - View Document
	Cl in ic a l & T r an sl at i o n a l S ci en c e Cen t er Participant & Clinical Interactions (PCI) Nursing/Coordinator Services Activity DocID: 1rllS - View Document