Oracle Clinical Data Management
Oracle Life Sciences Data Management Workbench is the only clinical trial data management solution that provides a validated, trustworthy single source of truth for all trial data that automatically reconciles data discrepancies and provides complete traceability. You’ll know immediately when something is going wrong with a trial and be able to take action.
Clinical trial data management in the post-COVID era.
The future of clinical data management
Get real-time access to trustworthy clinical trial data
Oracle Health Sciences Data Management Workbench gives you a complete, real-time picture of clinical trial data, providing visibility into the trial so that you can make better decisions quickly, effectively, and easily.
Reduce time, cost, and risk in collecting clinical trial data
Oracle Health Sciences Data Management Workbench provides you with a process-driven approach to simplify end-to-end clinical data flow, resulting in lower costs, increased quality, and lower risk.
Optimize high-volume clinical trial data processing
Oracle Health Sciences Data Management Workbench aggregates data from any source and provisions it to support you with analysis and reporting.
Collaborate with sponsors and CROs across clinical trials
Oracle Health Sciences Data Management Workbench improves study oversight and provides a single process for both in-house and outsourced studies.
Related clinical data management products and solutions
Clinical One
The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of the future.
Clinical One Data Collection
Clinical One Data Collection goes beyond electronic data capture, allowing you to collect datasets from any source and harmonize them in a single place.
Clinical One RTSM
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding.
Decentralized clinical trials
Virtual components in clinical trials allow greater patient participation and significantly improve clinical trial data quality.
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