nCartes CTMS clinical trial management reduces the time and cost of study data capture while eliminating study data errors. The sponsor cost and elapsed time of study data completion is materially reduced, while making it easier and chaper for sites to participate in sponsor trials.
- Enable sites to directly harness EHR source data and automatically populate study case report forms.
- Reduce elapsed time and cost of study data completion by using nCartes-sourced data entry.
- Increase data accuracy and reduce or eliminate data discrepancies for both numeric and text data.
- Materially reduce elapsed time and cost of source data verification (SVD) and study monitoring. nCartes automates Medical Records Abstraction (MRA), extracting relevant patient data directly from EHR systems without manual effort — giving sponsors clean, traceable data with full audit trails.