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Data managers and statisticians will be blinded throughout the trial.
Moreover, data analysts and statisticians will be blinded to group allocation.
Patients, investigators, monitoring members, outcome assessors, and statisticians will be blinded to group assignment and intervention.
The statisticians will be blinded to the randomized allocation of groups.
The principal investigators, clinical research assistants, drug administrators, patients and statisticians will be blinded.
Extensive multidisciplinary collaboration among biologists, toxicologists, epidemiologists, and statisticians will be needed to identify MOAs that describe the biological dose response process in a manner that is informative for modeling.
Similar(53)
The statistician will be given coded data to ensure blinding.
The statistician will be blinded with regard to treatment allocation.
The statistician will be blinded to the true group until the analyses are complete.
An independent statistician will be the only person with access to confidential participant data.
As was previously mentioned, the statistician will be blinded to participant condition.
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