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The approved protocol and subject informed consent states that data will only be accessible to the study team.
Human subject informed consent was obtained.
Human subject informed consent was obtained by the NYBC, under guidance of the NYBC committee for protection of human subjects.
The study protocol and subject informed consent document were approved by the Allendale Investigational Review Board, a central human investigation review board.
All patients who fulfilled the eligibility criteria were, prior to enrolment, asked to sign a Subject Informed Consent Form, in accordance with Danish data protection and privacy legislation, to allow access to their medical records.
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In addition, for investigations involving human subjects, informed consent has been obtained from the participants involved.
Moreover, the subjects' informed consent was obtained prior to the experiment.
In medical research on human subjects, informed consent requirements gained prominence in reaction to abuses.
The subjects' informed consent was obtained before any study-related activities.
All of the MCBS data are publically available and do not require subjects' informed consent.
Study subjects' informed consent and approval from the institutional ethical committee (University Hospital of Ioannina) were obtained.
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