CDNR PLATFORM
Organizations with on-going needs for biospecimens and clinical data may subscribe to CDNR platform to plan studies, identify patient cohorts for biospecimen collections and real-world data studies, and to manage biospecimen and associated clinical data requests:
- Platform contains massive historical clinical data that supports population analytics and study planning
- Researchers, CROs, biobank managers and others use CDNR to analyze data for patient cohorts based on very detailed clinical criteria, including demographics, primary diagnosis and co-morbidities, lab test results and medication history
- CDNR estimates patients and biospecimen numbers, and accrual timelines. Users can modify criteria and observe how these changes impact anticipated availability
- CDNR enables prospective and longitudinal collection of clinical data and biospecimens from patient cohorts so that researchers can observe changes during disease and treatment progression, better understand outcomes, etc.
- CDNR synthesizes all donor and biospecimen data for easy reference by end-user researchers; patient data is either anonymized or coded
- CDNR has received biopharma industry awards and customer accolades for ease of use and intuitive end-user experience
CDNR LICENSE
Novaseek offers license and on-demand implementation of the CDNR platform to the organizations that want to:
- Deliver superior transparency into clinical data at their sites for research
- Support real-world data studies and precision medicine programs and initiatives
- Facilitate biospecimen and associated clinical data acquisitions
- Streamline patient consenting and tracking for research within their own clinical sites
- Conduct site-specific clinical feasibility and patient cohort definition and recruitment
