What can TURBOARD do

for the Clinical Research and Trials Sector?

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.

What can TURBOARD do for the Clinical Research and Trials Sector?

  • Generate insights on clinical studies and review multiple study datasets to adjust development plans for trials and implement fail-fast policies.
  • Monitor trial safety, efficacy and data quality across the entire portfolio to rapidly respond to the protocol amendments.
  • Use templates to kickstart a project instead of starting it from scratch.
  • Share reports and analyses with teammates in real-time via the same platform.
  • Send reports and data to external recipients (with a single click and in various file formats).

Advantages of a Clinical Trials System Powered with BI Tools

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Reporting Performed manually or via outdated methods such as spreadsheets.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).
Time-saving: Eliminates manual data cleaning and entry, saving the clinical trial team from overwhelming data management processes while creating the necessary reports.
Cost-effective: An integrated solution that does not require dedicated IT/software/data science resources.
Minimizes errors: Preserves the integrity of clinical trial data and significantly reduces opportunities for error or overlooked insights via a single integrated platform for accessing and processing clinical data.
Faster decision-making: Provides insights and captures quality data to help accelerate decisions regarding changes, regulatory approvals, and quality improvements.

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