SOP 16. REPORTING REQUIREMENTS FOR UNANTICIPATED PROBLEMS,

First Page		Document Content
Date: 2014-03-10 08:07:42 Clinical research Pharmacology Drug safety Pharmaceutical industry Adverse event Institutional review board Food and Drug Administration National Institutes of Health Adverse effect Medicine Health Research		SOP 16. REPORTING REQUIREMENTS FOR UNANTICIPATED PROBLEMS, Add to Reading List Source URL: ohsr.od.nih.gov Download Document from Source Website File Size: 1,09 MB Share Document on Facebook

	Institutional Review Board Wake Forest University – Reynolda Campus Certificate of Confidentiality Checklist Note: A Certificate of Confidentiality will not be issued to an applicant co DocID: 1uZkR - View Document
	Institutional Review Board . ... . . DocID: 1ubXP - View Document
	University of Pennsylvania  Institutional Review Board O Is IRB Review Required? The first question one should consider when assessing the requirement for IRB review is whether the activity meets the regulatory defini DocID: 1tsSK - View Document
	Reliance Memorandum of Understanding Between and Among the University of California Campuses, UC Division of Agriculture and Natural Resources, and Lawrence Berkeley National Laboratory for Institutional Review Board Rev DocID: 1to8J - View Document
	INSTITUTIONAL REVIEW BOARD HUMAN SUBJECTS RESEARCH DETERMINATION FORM Instructions: Complete this form to help determine if your project qualifies as research that involves the use of human participants. You are not r DocID: 1tdGE - View Document