eCRF/ePRO Development
This service provides the development of tailored electronic case report form databases, management of eCRF/ePRO systems, and CDISC/CDASH-compliant databases, including data coding and adverse event management, to ensure the collection of high-quality, traceable data. This service provides comprehensive design, implementation, and validation of paediatric-specific CRFs/eCRFs, as well as secure management of paediatric clinical trial data, with systematic data cleaning, query resolution, and handling of missing or inconsistent data. Special attention is given to paediatric-specific variables, including age-adjusted dosing, developmental assessments, and safety parameters, ensuring that datasets are accurate, reliable, and suitable for downstream analysis and report preparation.
