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Currently, these high-/medium-throughput test models avoid the main questions referring to why an adverse scar forms instead of a normotrophic scar and what causes a hypertrophic scar to form rather than a keloid scar and also, how is the genetic predisposition of the individual and the immune system involved.
Once all data, including the adverse event forms and primary source documents, were received, they were reviewed using a structured abstraction form.
All events either mild or serious were recorded on adverse effect forms.
Hospitalization information was obtained from the IMPRESS trial's standardized case report and serious adverse event forms.
All but two adverse events forms were returned.
Treating therapists were also asked to complete adverse event forms.
We used standardised serious adverse event forms for reporting (serious) adverse events.
All study participants were informed of the study's safety policy and given adverse event forms at baseline.
Identifying an adverse effect forms the basis for hazard identification and for defining the critical effect for quantitative risk assessment.
All AEs were recorded on adverse event forms and evaluated by the investigator for causality for the relationship to the study feeding and for severity.
All AEs are recorded in adverse event forms and are evaluated by the investigator for causality for the relationship to the study feeding and for severity.
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CEO of Professional Science Editing for Scientists @ prosciediting.com