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Our Process

We systematically test digital health technologies so life science companies, health systems, and digital health companies have the insights needed to advance product development and enhance patient impact.

Our Focus

At datosX, we systematically test digital health technologies so life science companies, health systems, and digital health companies have the insights needed to advance product development and enhance patient impact.

Our unique platform connects hospital systems and digital health companies for seamless end-to-end trial execution, enabling:

What we do

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Protocol development

We design protocols that meet sponsor’s unique needs and adhere to regulatory standards with scientific rigor.


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Health System matching

We tap into our extensive health system network to pair partners that are optimally matched.


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Comprehensive trial execution

Our experienced team of physicians, trial experts, and statisticians oversees the successful execution of studies from start to finish.

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Data capture & analysis

We ensure accurate and robust data analysis to enable everything from FDA submissions and investor reporting to preparing for journal publications
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Technology Validation

Generate the validation data you need to expedite regulatory submissions, support clinical publications, substantiate market claims, and more.

Partnership Opportunities

Collect pivotal data in partnership with leading US health systems with a vested interest in testing your solution

Enhanced ROI Analysis

Use study insights to evaluate your Go-To-Market strategy, ensure impact, and support your ROI analyses.

Healthcare System Matching

From contracting and onboarding the selected healthcare system to identifying the principal investigators, research coordinators and sites needed for the trial – datosX sources the most appropriate study partners from across our diverse network.

Protocol development

From engaging regulatory and therapeutic area subject matter experts (SMEs) to overseeing protocol IRB submissions, we work with clients to develop the optimum protocol.

Comprehensive trial execution

Pre-trial
We perform several core pre-trial activities including developing an overarching project plan, recruitment strategy and coherent documentation process. This preparation ensures a smooth trial start.

During-trial
During the trial we manage all clinical and operational issues, keeping sponsors up to date on trial progress, challenges, and outcomes.

Post-trial
We coordinate the collection and management of all documents required for regulatory reports and provide a final summary / study readout to sponsors.

Data capture & analysis

Pre-trial
We develop operations and processes to capture data securely and reliably, including the ePRO data collection tool (if needed)

During-trial
We conduct Source Data Verification to confirm completeness and accuracy of data entry.

Post-trial
We provide final statistical analysis of study data in addition to manuscript writing support (if needed)

Health Systems
​Digital Health Companies
Life Science Companies
Venture Capital