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Discover LudwigThe phrase "acquired informed consent" is correct and usable in written English.
It is typically used in contexts related to research, medical procedures, or legal agreements where individuals are informed about and agree to participate or allow something to happen.
Example: "Before starting the clinical trial, the researchers ensured that all participants had acquired informed consent."
Alternatives: "obtained informed consent" or "secured informed consent."
Exact(2)
The survey acquired informed consent from mothers of the children included in this study before asking any questions and before obtaining biologic and anthropometric measurements.
The first series of specimens ('M' samples) was collected in an anonymous manner from patients according to Finnish laws and regulations by the permission of the director of the health-care unit, and the other series included specimens ('MY' samples) from patients with an acquired informed consent.
Similar(58)
Researchers say that the controversy prompted some trials involving infants to halt work while organizers reviewed and revised materials used to acquire informed consent.
Hospitals will be matched in comparable pairs in terms of 1) the number of deaths per year for the participating geriatric wards, and 2) the motivation of the participating wards in terms of the number of patients from whom they will acquire informed consent for participation in the baseline measurement period.
This study was approved by the Hirosaki University Ethics Committee and we acquired written, informed consent for this study from patients and/or family.
It found women were often not properly appraised of less invasive and risky alternatives, such as physiotherapy, and that doctors did not acquire fully informed consent.
DNA was obtained from the peripheral blood of the affected and healthy family members after acquiring written informed consent.
Blood was acquired from informed, consenting individuals according to institutional guidelines, and DNA extracted using established protocols.
HCPs provided study information to patients and Health Insurance Portability and Accountability Act (HIPAA) informed consent was acquired from all study participants.
Blood samples were taken and demographic and clinical data were recorded from all patients enrolled in the study after written informed consent was acquired from patients or their next of kin.
Written informed consent was acquired from every participant prior to participation.
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CEO of Professional Science Editing for Scientists @ prosciediting.com