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Both the study protocol [ 58] and the full search strategy [ 58] were registered before initiation of the search.
All authors were deeply involved and contributed actively to development of both, the study protocol and the manuscript.
The Colorado Multiple Institutional Review Board approved both the study protocol and a waiver of informed consent.
Both the study protocol and an earlier wave of data (2008) comparing deceased cancer patients in Belgium and the Netherlands have been published [ 4, 15, 16].
This may be achieved, most directly, through the use of appropriate terminology in both the study protocol and standard operating procedures documents: in avoiding the use of dogmatic excessively or didactic language, interventions may be implicitly permitted appropriate levels of flexibility in intervention delivery, whilst maintaining fidelity to the original study protocol.
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Local institutional review boards and independent ethics committees, or both, approved the study protocol and informed consent forms before use.
The Medical Ethics Committees of both hospitals approved the study protocol and opt-out consent method.
BROD developed the concept for the study and both authors designed the study protocol.
Both authors modified the study protocol, contributed to the analysis of data and wrote the paper.
Institutional review boards at both universities approved the study protocol, and all participants provided written informed consent.
The local medical ethics committees of both hospitals approved the study protocol, and informed consent was obtained from patients or their legal representatives before inclusion.
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