TURBOARD OEM Solutions

for Clinical Trial Management Systems

Empower Your Clinical Trials Software

with Business Intelligence and Analytics Platform


Advertising your product without BI features can be difficult. You need a strategic, experienced BI partner that provides OEM services to ensure hassle-free, cost-effective and lucrative sustainable outcomes.

Enhance your CTMS software with TURBOARD's OEM services to deliver unparalleled analytics capabilities. By integrating our advanced BI tools, you can offer your clients more robust data processing, insightful analytics, and interactive reporting features.

This integration enables CTMS software providers to stand out in the market, offering a more comprehensive solution that not only streamlines clinical trial management but also provides deep insights into trial data, ultimately leading to more informed decisions and successful outcomes. Click here to discover more about TURBOARD's capabilities in the Clinical Research and Trials sector.

Why choose as your OEM partner?

Our Experience in BI & Data Analytics

  • A prospering BI software,
  • Chosen by many reputable clients from various business sectors,
  • Utilized by over 250K users all over the world,
  • Experienced in big data ecosystems,
  • Experienced in the field of Pharmaceuticals and Clinical Data.

Our Experience in OEM

  • 16 years of OEM partnership with PharmaCircle serving more than 100 international pharmaceutical companies comprising 79% of big pharma organizations,
  • Exclusively chosen by the Ministry of Health of Turkey to develop the SİNA application.

Adding features and developing analytics capabilities in-house for your clinical trials’ software requires a dedicated team of BI experts, developers, designers, and data scientists, which can be very costly and time-consuming. On the other hand, you may consider partnering with an experienced BI vendor.

We would be happy to combine our expertise with yours!

By considering TURBOARD as an OEM partner for BI integration into your software, you will earn advantages other alternatives cannot provide, as outlined below:

With Other BI Vendors By Partnering with TURBOARD
Pricing
  • Expensive
  • Fixed price
  • Upfront payments
  • Paid support services
  • Flexible pricing
  • No upfront payment
  • Revenue-sharing model
  • Support service included in package
Time to Market
  • Takes longer to integrate with your system
  • Fast integration due to previous domain expertise and enthusiastic support
Flexibility & Extensibility
  • Insufficient, not very flexible in developing a tailor-made platform to your needs
  • Lacks deep experience in your domain
  • Thorough examination of the case and its particular needs prior to start
  • Vast experience in domain
  • Continuous correspondence and feedback sessions
  • Software updated with latest industry demands
Support
  • Limited until the integration is complete or, if continuous, would be costly
  • Experienced and devoted support team

Sample Showcases Demonstrating TURBOARD’s Analytic Capabilities in Clinical Trials Data

The data is automatically collected and made available to users from various up-to-date, open source clinical databases.

These reports and analytics can be viewed according to various dimensions, such as study duration, purpose, type, masking type, trend, diseases, sources/sponsors, therapeutic areas, trials count, success status and rates, and more, with drilling-down and slicing options.

By monitoring these analyses, a sponsor can adjust a trial development plan, compare the performances of sponsors, and decide whether to opt for a certain clinical trial or apply a fail-fast policy to eliminate it. The sponsor will earn insights into:

  • The number, type, masking type, etc. of clinical studies,
  • Number and success rates of completed trials,
  • Trials’ participants and volunteers,
  • Trials hitting primary endpoint.
  • Trend analysis of trials’ diseases, sources, etc.,
  • Diseases with the highest share of completed and successful trials,
  • Companies with the highest count of completed and successful trials,

    

Trial sponsors and CROs can monitor, follow up, and prepare any kind of report for their ongoing clinical trial(s) via a perceptive platform. For a selected clinical trial, users can monitor participants’ recruitment data, eligibility, visit/lab/test results, and rating scales’ details.

1. Subject Recruitment: Trial participants’ reports and analyses with multi-filters and slicing options.

  • Inclusion/exclusion,
  • Demographic and location check,
  • Age and gender dimensions,
  • Eligibility reports,
  • Dropout and screen failure rates,
  • Subject scores with standard deviation analysis.


2. Visit Analysis: Visualized reports and analysis of lab results, values, and visits with multi-filters and slicing options.

  • Active/Placebo criteria,
  • Gender filters,
  • Visits check: count, dates, over trial’s periods, etc.

    

3. Scale Outcome: Visualized reports and analysis of rating scale outcome with multi-filters and slicing options.

  • Outlier analysis,
  • Real-time situation check on matrix,
  • Comprehensive adverse events analysis: by severity, seriousness, status, gender, study arms, doses intensity, etc.

    

To reveal striking insights hidden in your own data, discover

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