Business Intelligence Solutions for Clinical Research and Trials
Performing a clinical trial is time consuming, expensive, and requires refinement and precision. Companies experience enormous pressures to obtain regulatory approvals and expedite the process of serving their products on time.
Clinical data collection, entry, validation, and reporting are key factors to a successful clinical trial, but once a clinical trial begins, data processing and the preparation of numerous reports for medical monitors, regulatory authorities, stakeholders, and investors can take its toll on the project.
TURBOARD helps researchers and CROs to blend data from multiple data sources and provides a united analysis platform that accelerates the lifecycle of the trials, reduces costs, and accesses insights at a faster rate.
Without TURBOARD | With TURBOARD | |
---|---|---|
Reporting | Performed manually or via outdated methods such as spreadsheets. | Sophisticated and automated reports/dashboards for regulatory authorities and/or stakeholders. |
Data Analysis | Does not provide at all or is limited to certain types of clinical trials. | Agile tools that fulfill data processing requirements, and provide insightful analytics and risk-based monitoring. |
Data Integration | The clinical trial lifecycle is completed via multiple standalone tools and solutions. | Processed via a single integrated platform that enables all participants across the lifecycle of the clinical trial to work as a team (CROs, sponsors, biostaticians, medical monitors, and stakeholders). |
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