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1  of ICU admission, or if a surrogate was readily available, consent was sought prior to initial sample collection; otherw
2 n; otherwise, a waiver of consent was granted, and deferred consent was sought 3 days later.
3  This scoping review of the literature on requesting family consent was prepared to support of the development of leading
4                                                    Informed consent was obtained for MR imaging.
5                                                    Informed consent was obtained from all participants.
6                                                    Informed consent was obtained from all patients.
7                                                    Informed consent was obtained from all subjects.
8                                                    Informed consent was obtained prior to enrollment.
9                                                    Informed consent was provided according to the last will of the donors
10 ondition and the poor prognosis to the patient, an informed consent was obtained after she opted for medical termination
11                                                 An informed consent was obtained after she opted for medical termination
12 study had institutional review board approval, and informed consent was obtained from 72 patients with breast cancer befo
13 study was approved by the ethics review board, and informed consent was obtained.
14 titutional review board approval was obtained, and informed consent was waived in this HIPAA-compliant retrospective stud
15 as approved by the institutional review board, and informed consent was waived.
16 review board approved this retrospective study and informed consent was waived.
17 titutional review board approval, and the need for informed consent was waived.
18 titutional review board; the requirement to obtain informed consent was waived.
19 proval was obtained, and the requirement to obtain informed consent was waived.
20 tional review board, and the requirement to obtain informed consent was waived.
21                          The requirement to obtain informed consent was waived.
22 proved chart review, and the requirement to obtain informed consent was waived.
23 rd approved this retrospective study and waiver of informed consent was obtained.
24 retrospective, HIPAA-compliant, multicenter study; informed consent was waived.
25                                            Written informed consent was obtained from 67 consecutive patients (57 years +
26                                            Written informed consent was obtained from all participants before enrollment
27 was approved by the local ethics board and written informed consent was obtained from all participants.
28 /- SD, 34.3 +/- 6.5 y) were recruited, and written informed consent was obtained from all participants.
29                                            Written informed consent was obtained from all participants.
30                      Materials and Methods Written informed consent was obtained from all patients, and the study protoco
31 ational Research Ethics Service Committee; written informed consent was obtained from all patients.
32 y had institutional review board approval; written informed consent was obtained from all patients.
33                                            Written informed consent was obtained from all patients.
34 ved by the institutional review board, and written informed consent was obtained from all study participants.
35 proved by the local ethics committees, and written informed consent was obtained from all subjects prior to enrollment.
36 multi-institutional HIPAA-compliant study; written informed consent was obtained from all subjects.
37                                            Written informed consent was obtained from all subjects.
38 pproved by the local ethics committee, and written informed consent was obtained from each patient.
39 pproved by the institutional board review; written informed consent was obtained from healthy subjects and was waived for
40                                            Written informed consent was obtained from patients or their parents.
41                Materials and Methods After written informed consent was obtained, 8869 women (age range, 29-85 years; mea
42 maging datasets were acquired at 3 T after written informed consent was obtained.
43 by age, and interviews occurred only after written informed consent was obtained.
44 d by the institutional research board, and written informed consent was obtained.
45                                            Written informed consent was waived.
46  prior to initial sample collection; otherwise, a waiver of consent was granted, and deferred consent was sought 3 days l
47 s Institutional review board approval was given and patient consent was not required for this study.
48                      Materials and Methods Informed written consent was obtained for all procedures and the study was app
49                                            Informed written consent was obtained from all participants prior to entry int
50 eview board, and the requirement to obtain informed written consent was waived.

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