FDA [Food and Drug Administration] waives IRB [Institutional Review Board] review of certain clinical studies of azidothymidine (AZT)
IRB: A Review of Human Subjects Research 1986 November- December; 8(6): 11
Showing items related by title, author, creator and subject.
Unknown author (United States. Food and Drug Administration, 1983-01)
A Study of Warning Letters Issued to Clinical Investigators and Institutional Review Boards by the United States Food and Drug Administration Gogtay, N J; Doshi, B M; Kannan, S; Thatte, U (2011-10)Warning letters (WLs) issued by the US FDA (United States Food and Drug Administration) mention the nature of violations by clinical investigators and institutional review boards (IRBS) and can help as training tools.
A Study of Warning Letters Issued to Institutional Review Boards by the United States Food and Drug Administration Bramstedt, Katrina A.; Kassimatis, Katy (2004-12)