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For legal and ethical reasons, waived consent is "an area where universities are concerned that they not make a mistake," Dr. Cheung explained.
But in 1994, the government changed its rules regulating the conduct of research on humans, saying patients could be enrolled under so-called waived consent as long as the community at large was notified that the experiment was under way and family members, having been told of it once they were found, were allowed to remove patients from it.
The IRB waived consent for the study.
The research ethics board of Sainte-Justine Hospital approved waived consent for this study.
This has lead to a number of publications on community consultation on the specific issue of waived consent.
Can surrogate consent be a fair and ethical solution, or can we ask for waived consent and, if so, under what circumstances?
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While some medical ethicists opposed waiving consent, the FDA approved the proposal in August 1998 for five medical centers.
A number of studies have suggested that members of the public are more willing to waive consent when they understand the issues involved in carrying out such studies.
The requirement for signed written consent was waived, as consent was implied by participants completing and submitting the survey.
Salus IRB waived informed consent.
The University of California San Francisco Committee on Human Research approved this study and waived patient consent requirements.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com