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Other safety outcomes were clinical AEs, relevant laboratory measurements (peripheral eosinophil counts, liver function and haemoglobin), maximal helminth infection intensities during the study and requirement for additional anthelmintic treatments.
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Recruited women were interviewed and given a description of the study and requirements for participation in the project.
Prior to beginning data collection, participants were given the opportunity to ask any questions about the study and requirements of their involvement.
Four established human breast tumour cell lines with different biologic properties were selected for study and requirements for their clonogenic growth in semisolid cultures were identified.
The Institutional Review Board approved this retrospective study and the requirement to obtain informed consent was waived.
The Institutional Review Board approved this retrospective study and the requirement to obtain informed consent was waived (IRB #: 13-139B).
The narrow selection criteria in this study and the requirement to stay in hospital contributed to the screening of a very large number of patients.
The institutional review board at Partners HealthCare System approved the study and the requirement for informed consent was waived.
Approval of the University Ethics Committee was obtained before the study and the requirement for informed consent from patients was waived because of the observational nature of the study.
Following provision of written consent, panel members provided an information letter via email outlining specific details relating to the overall aims, study procedures and requirements of the study.
In the current study, the researchers presented the study outline and requirements of participants (clinician and patient) to oral and maxillofacial surgeons at a continuing professional development meeting.
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