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All participants in this study consented voluntarily.
All patients involved in this study consented to participate in the study and publication of its results.
Before the initiation of treatment, all patients included in this study consented to the possibility of being included in a study with a retrospective design in the future and publication of their data in an anonymized fashion.
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As in the cohort of this study, consent to use register data was likely to compensate for mental disorder bias.
All consumers who were invited to participate in this qualitative study consented to do so.
All cartilage specimens in this study were consented under an IRB-approved protocol of informed consent through Hôpital Necker-Enfants Malades.
The selected subjects were informed about this study and consented to participate.
All participants in this study had consented to take their treatment and had a certain level of adherence at baseline.
All participants provided verbal consent for this study; verbal consent was approved by our Institutional Review Board.
There was no verbal or written informed consent for this study, as consent of the salesperson would have undermined the simulated client methodology.
There was no verbal or written informed consent for this study, as consent of the salesperson would have undermined the simulation.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com