Governor Signs Adverse Event Reporting Bill
Minnesota Medicine 2003 September; 86(9): 98
Showing items related by title, author, creator and subject.
Unknown author (2009-03-29)
Finn, Robert (2000-05-17)
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)