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Aliquots of normal bone marrow were obtained from four normal allogenic bone marrow donors granting written informed consent and as approved by the Johns Hopkins Medical Institute Institutional Review Board (J0002).
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All participants received a complete description of the study and granted written informed consent.
The patient granted written informed consent for conducting the genetic test as required by our institutional review board.
Prior to study inclusion, all participants received a complete description of the study and granted written informed consent according to the Declaration of Helsinki.
All participants granted written informed consent.
The ethics committee of each institution approved this study, and all patients granted written informed consent.
The parents of the patient granted written informed consent for publication of this report as the patient was underage.
Consequent upon granting a written informed consent, the clinicians and field assistants obtained the following information from the child's health card: date of birth (DOB), birth order, sex, place of birth and dates of the administered vaccines.
The trial protocol, which complied with the declaration of Helsinki, was reviewed and approved by the pertinent National Ethics Committees, and all patients granted their written informed consent to participate.
Tenets of the Declaration of Helsinki were followed, institutional review board approval was granted, and written informed consent was obtained from all participants.
The institutional review board of all participating centres granted approval and written informed consent was mandatory.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com