Guidance on Reporting Adverse Events to Institutional Review Boards for NIH-Supported Multicenter Clinical Trials
Bethesda, MD: National Institutes of Health, 1999 June 11; 3 p. [Online]. Available: http://grants.nih.gov/grants/guide/notice-files/not99- 107.html [2002 September 17]; 3 p.
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Draft Guidance for Industry on Using a Centralized Institutional Review Boards Process in Multicenter Clinical Trials; Availability Unknown author (United States. Food and Drug Administration, 2005-03-28)