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Compliance will be assessed by return of study drugs and drug bottles with electronic track caps.
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Informed consent was implied by the return of study questionnaires, as approved by institutional review boards.
Consent to participate in Phase 1 of the study was implied by return of the postcard and completion of survey.
Consent to participate in the study was assumed by return of a completed questionnaire.
Consent was implied by return of questionnaire.
Compliance was determined by pill count of returned bottles of study medication.
By returning to his study of economics, he felt he would be able to understand more thoroughly what was occurring in the world.
A validated FFQ was mailed to participants who had answered the RFQ and was returned after completion by 79.6% of study participants in three centers (CCO, USC, and UH).
Pre-treatment, there was one case of Grade 1 neutropaenia (1600 × 10/l) in the group that received the non-fixed combination first; this subject returned to normal by Day 7 of Study Period 1.
I have certainly benefited by returning to further studies – a PhD in education at Goldsmiths College – where I have been amazed by the skills of the education lecturers.
Patient compliance was assessed at each visit by quantifying the amount of study medication returned.
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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