Home > Newsletters > The QMN Weekly Bulletin > FDA Warns Trial Investigator for IRB, Consent Form, Protocol Violations
The QMN Weekly Bulletin
Nov. 9, 2012 | Vol. 4 No. 45
FDA Warns Trial Investigator for IRB, Consent Form, Protocol Violations
The FDA handed a cardiac surgeon at Washington, D.C.-based Washington Hospital Center a warning letter for not having institutional review board (IRB) approval when recruiting some patients into a clinical trial.
During an Aug. 24 to Sept. 15, 2011, inspection, investigators found five subjects recruited into an investigational drug study had signed consent forms indicating the trial was IRB-approved. But according to the Sept. 28 letter posted recently online, IRB approval had expired in early May of that year. Patients were still being recruited through July, the letter adds.
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