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Our Data
Our patent-pending algorithms run on top of the iTrials Data Universe to identify optimal trial/investigator sites and high density groupings of pre-qualified patients. Designed and developed specifically for this purpose, this proprietary database and service platform aggregates provider and patient information from a variety of sources, including: claims clearinghouses, electronic medical record providers, independent physician associations, pharmacy benefit management providers, and a variety of other healthcare data sources.
For each of the approximately 80 million individual patients in our database, we have compiled data from a variety of disparate data sources to create de-identified longitudinal health histories for each patient.
By drawing upon information from dozens of data sources, the iTrials Data Universe transcends the limitations of any single data feed or type. iTrials is thus able to determine the prospective eligibility of providers, trial sites, and patients much more accurately and reliably than is enabled via any other means in the market today.
Our Tools & Processes
iTrials develops and deploys uniquely tailored, client-specific strategies to identify high potential sites and patients. This approach is rooted in the understanding 1) that every trial sponsor’s needs are unique and 2) that the up-front ability to modify and fine-tune a patient recruiting strategy, based on the results of a data-driven analysis, quantifiably improves a clinical trial’s ultimate chances of success.
iTrials proprietary tools and models assess the cause and effect of real-time adjustments to numerous study parameters such as:
Inclusion & exclusion criteria,
Physician and investigator performance,
Local and regional media market metrics,
Proximity to required facility resources, and more.
Ultimately, iTrials clients receive compelling analysis tools and reports that offer a uniquely actionable series of recommendations for protocol feasibility, site selection and patient recruitment.
The Results
iTrials assumes responsibility for identifying target sites and high probability patients, so trial sponsors can focus their resources and attention on other critical tasks, activities, and objectives.
Our clients plan and launch clinical trials with a never-before-available understanding of the expected costs, trial duration, complexities, and scope. Such perspective and understanding helps our clients optimize the investment of every dollar.
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