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Institutional review boards at each participating site approved the study and all participants provided informed consent.
A properly constituted Research Ethics Committee at each participating site approved the study, and each participant provided written, informed consent.
All participants were enrolled under Institutional Review Boards or ethics committee approval at each participating site.
Ethical approval was obtained at each participating site, and a written informed consent was given by all study participants.
Each participating site is responsible for the recruitment and scheduled follow-up visits of participants.
Instead, I went to each participating site and shopped for shows I might want to copy.
The study was reviewed and approved by the institutional research ethics committees of each participating site.
Administrative data from each participating site were examined for utilization trends.
For our Workgroup, we selected all participating site URLs as the most relevant content.
IncobotulinumtoxinA was applied according to the individual treatment algorithms of each participating site and additional antispastic treatments were allowed.
The study protocols, procedures, and consent statements were approved by the Institutional Review Boards (IRBs) of each participating site.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com