Governor Signs Adverse Event Reporting Bill
Minnesota Medicine 2003 September; 86(9): 98
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Adverse Event Reporting -- Improving Human Subject Protection. Guidance for Clinical Investigators, Sponsors and IRBs Unknown author (United States. Food and Drug Administration [FDA]. Office of the Commissioner (OC) Center for Drug Evaluation and Research [CDER] (United States); Center for Biologics Evaluation and Research [CBER] (United States); Center for Devices and Radiological Hea, 2007-04)