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The goal is to create databases, with the consent of the study subjects, that would be open to all doctors and researchers.
Their aim is to put the vast and growing trove of data on genetic variations and health into databases — with the consent of the study subjects — that would be open to researchers and doctors all over the world, not just to those who created them.
All subjects have given written informed consent of the study.
Consent of the study participants was obtained before taking the samples for stool examination.
The verbal consent of the study respondents were documented using tape recorders.
The informed consent of the study was obtained from all patients.
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The GPs had given permission for further contact at the time of consent to the study.
Waiver of consent for the study was obtained from the Intermountain Office of Research.
As the majority of the population in the study area was illiterate the IRB endorsed oral consenting of the study participants.
The patient died 30 days after withdrawal of informed consent for the study.
After submission of the signed consent form of the study participants („informed consent"), patient enrollment takes place in the participating rehabilitation centres based on the assessment of the inclusion and exclusion criteria by the attending physician.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com