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The top documents tagged [fda regulated product]
ClinicalTrials.gov Why Does it Affect Me? Should I Be Concerned? Presenter Name and contact Info
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mHealth Israel_Physio Logic_US and EU Digital Health Regulatory Landscape
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How the Past Influenced Human Research Protection Regulations Shirley J. Hicks Director, Division of Education and Development Office for Human Research
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Constance Lewin, M.D., M.P.H. Associate Director for Human Subject Protection Acting Branch Chief, Good Clinical Practice Branch 1 Division of Scientific
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Council for Responsible Nutrition Supplyside West, October 19, 2006 The Case for Mandatory Reporting of Adverse Events for Dietary Supplements Steve Mister
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Human Research Protection Program 101 March 19-20, 2007 Cincinnati, Ohio
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Exempt and Expedited Reviews What Requires IRB and R&D Approvals
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