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Another aspect of genetic information with significant legal implications involves informed consent.
The human investigation committee of the Yale institutional review board approved the derivation (retrospective) phase with a waiver of informed consent, and the validation (prospective) phase involved written informed consent from all patients.
All patients involved provided informed consent.
All the patients involved provided informed consent.
All samples were gathered with full ethical consent and appropriate documentation as stipulated by the ethical consent, which normally involved written informed consent.
Studies on material of human origin were approved by the ethics committees of the universities involved, and informed consent was obtained from all donors or their guardians.
The study was approved by the Ethical Committees of all Institutions involved and informed consent was obtained from all individuals studied.
This study was approved by the institution review board of Ren Ji Hospital which is affiliated with Shanghai Second Medical University, and each patient involved gave informed consent.
The tissue samples were obtained during routine surgery at the Department of Orthopedics of the University of Regensburg, where approved by the local ethics committee and patients involved gave informed consent.
Ethics approval for the RCT was granted from Curtin University and each of the hospital Health Services involved and informed consent was obtained from each participant prior to them completing any questionnaire.
Because our goal was to develop new ways to assess manuscript decision-making and publication bias, and because it could in no way influence the fate of manuscripts being discussed, our project did not involve written informed consent.
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