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The protocol and informed consent received regional ethics committee approval and study subjects provided full consent prior to participating in any study-related procedures.
A classic model of regulating the use of human materials for research objectives is the "informed consent" received by a researcher from a patient, confirming commitment to provide personal biological material for a certain kind of the research as well as a decision of a bioethical commission (an ethic committee) made about moral acceptance of the conducted research objectives and methods.
At the screening visit, women were interviewed to confirm understanding and willingness to comply with study requirements, completed written informed consent, received HIV pretest and condom counseling, and underwent oral mucosal transudate (OMT) rapid HIV testing.
Eligible women who gave informed consent received a postal questionnaire.
5) Consent received from the participant's General Practitioner.
The concept of informed consent received a great deal of attention during the 1980s in Japan.
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Our data raises questions over the meaningfulness of the expressions of non-consent received in this study.
At the end of the 7-year study period, all men who consented received a biopsy.
Women who consented received vaginal and perianal swabs at 31 33 weeks, 35 38 weeks and during labour.
Children whose parents consented received a dental examination and the clinical data was collected on mark sense cards.
Written informed consent was received from patients.
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CEO of Professional Science Editing for Scientists @ prosciediting.com