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The process of obtaining informed consent for subject participation in clinical research protocols is multifaceted and includes the researcher and subject or guardian reviewing the study purpose, procedures and informed consent document.
Designing and conducting clinical research protocols involve the planning and the making of intelligent, informed decisions from the start.
However, DTI images of the optic nerve may show severe geometric distortion, in particular in the region of the orbital apex, and fibre tracking of the optic nerve is still part of ongoing clinical research protocols.
In addition to being involved with BPRU clinical research protocols, I've also gotten involved with several pharmaceutical company studies and have acted as the clinical research coordinator on those projects.
Some agency personnel may not have had prior experience with clinical research protocols and may be unfamiliar with screening potential subjects; these personnel are likely to be employed in agencies unaffiliated with academic health sciences centers.
To evaluate a clinical classification system, the Clinical Age-Related Maculopathy Staging (CARMS) system, for age-related maculopathy (ARM) using a simple grading scale designed for clinical practice and clinical research protocols.
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This chapter is designed to increase the skills of clinical researchers and research sponsors to identify and address the ethical considerations of different sections of a clinical research protocol.
The clinical research protocol was approved by the Institutional Review Board (IRB) of each participating metabolic clinic.
Data management is one of the most critical areas in any clinical research protocol.
This research was conducted according to a clinical research protocol (DR08-0066) approved by the MD Anderson Institutional Review Board.
This battery is part of a clinical research protocol designed to track auditory development in this population.
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