The eCRF technology goes hand-in-hand with ePRO solutions for clinical trials. Electronic Case Report Forms (eCRF) are cost-effective and timely and also scale down the likelihood of human error while tracking and analyzing patient data.

CROS NT applys Oracle’s RDC (Remote Data Capture) Onsite program to conduct studies which enables a single portal for data input and the ability to produce highly organized and standardized information.RDC Onsite contains a patient casebook spreadsheet which can quickly communicate the status of all CRFs in the system.

Data accuracy and timeliness is substantially improved using RDC Onsite for CRFs. The system provides edit checks, patient validation and batch validation. The “discrepancy navigator” also addresses all discrepancies with a CRF and allows users to communicate the discrepencies between different groups involved in the study.

Onsite also allows Monitors and Investigators to verify and approve CRFs one at a time and provide an electronic signature on approval. Finally, the Patient Data Report consisting of a single PDF file can be created for all patient CRFs.

The electronization of of CRFs allows more for improved data accuracy and data entry efficiency in less time. Electronic CRFs improve organization within clinical trials and provide at-a-glance overviews and ready-to-access CRFs.

CROS NT’s Clinical Data Management department works with eCRFs including CRF design and review and CRF tracking.