There are compelling medical, ethical, and legal arguments that support mandating use of a central institutional review board (CIRB) for the review of clinical trials performed at multiple institutional sites. Progress against serious diseases depends on this.
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19.
See Check et al., supra note 10; K. E.Flynn, C. L.Hahn, J. M.Kramer, D. K.Check, and C. B.Dombecket al., “Using Central IRBs for Multicenter Clinical Trials in the United States,”PLOS ONE8, no. 1 (2013): e54999.
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B.Ravina, L.Deuel, A.Siderowf, and E. R.Dorsey, “Local Institutional Review Board (IRB) Review of a Multicenter Trial: Local Costs without Local Context,”Annals of Neurology67 (2010): 258-260.
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A. R.Stark, J. E.Tyson, and P. L.Hibberd, “Variation among Institutional Review Boards in Evaluating the Design of a Multicenter Randomized Trial,”Journal of Perinatololgy30 (2010): 163-169.
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See Ravina et al., supra note 20; The Lancet Neurology. “NeuroNEXT: Accelerating Drug Development in Neurology,”The Lancet Neurology11 (2012): 119; P.Kaufmann and P. P.O'Rourke, “Central Institutional Review Board Review for an Academic Trial Network,”Academic Medicine90, no. 3 (2015): 321-323.