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1 mpliant institutional board approved multicenter study, and all participants provided written informed consent.
2 The institutional review board approved the study and all participants provided written informed consent.
3 All participants provided written informed consent.
4 tional review board-approved study was HIPAA compliant, and all participants provided written informed consent.
5 utional review board of each participating institution, and all participants provided written informed consent.
6 on Trial II study was approved by the ethics committee, and all participants provided written informed consent.
7 All participants provided written informed consent.
8 All participants provided written informed consent.
9 After study approval by the local ethics committee, all participants provided written informed consent.
10 his study received institutional review board approval, and all participants provided written informed consent.
11 e study was approved by the institutional review board, and all participants provided written informed consent.
12 view board approval was obtained at each clinical site, and all participants provided written informed consent.
13 This study received ethics approval, and all participants provided written informed consent.
14 The study was approved by a regional ethics committee, and all participants provided written informed consent.
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