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All participants in the study provided informed consent, as per the requirements of Research Ethics Review Board of the researcher's institution and research site institutions.
You both also need to be over the age of consent as per your relevant state or territory.
All patients provided written informed consent, as per institutional guidelines.
All participants gave informed written consent as per ethical approval.
All participants gave informed, written consent as per the Declaration of Helsinki.
This study was deemed eligible for abbreviated consent as per Federal regulations.
Similar(45)
Researchers must foresee third-party consent as a major encumbrance.
Black Americans were more likely to consent than Asian Americans (P < 0.001) and as likely to consent as white Americans.
Approval for the study was also provided by the District Children's Officer (DCO), and we obtained a waiver of individual guardian consent because as per human subjects regulations, the study was minimal risk, the study could not have been practicably carried out without the waiver, and because the waiver did not adversely alter the risk-benefit ratio for participants.
Consent was verbal as per protocol approved, since dealing with healthy control blood.
Verbal informed consent was obtained as per guidance provided by the IRB, since this is an observational study where no personal information was recorded, thus anonymizing the study data.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com