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A trial nurse responsible for obtaining informed consent was requested to present standard informed consent information on the microbicide study to the 18 women in the non-intervention group, in addition to health information on cervical cancer, and was advised to allow the women to ask questions.
Informed consent was requested at the start of the questionnaire.
Following interviews, further informed consent was requested to access medical records.
For minors, the informed consent was requested from their parents/guardians.
As the patient recovered consciousness, deferred informed consent was requested from the patient.
Depending on the national requirements, written or oral informed consent was requested.
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Written informed consent is requested from all patients prior to participation in the study.
In research, it is common practice that extensive informed consent is requested, whereas traditionally, there is no (or little) feedback of results.
A written informed consent is requested concerning participation in the study, employment data from the employers' records, as well as dates and diagnoses of SA from the medical records of the OHS.
Informed verbal consent was requested from each study subjects.
If the patient had died or was not mentally competent to give informed consent, consent was requested from the patient's next of kin or the individual who had legal authority to consent on behalf of the patient.
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CEO of Professional Science Editing for Scientists @ prosciediting.com