For Medical Researchers
Accelerate discovery with high-quality, diverse and ethically sourced health data
Why ConsentHealth?
ConsentHealth offers direct access to health data contributed and consented to by individuals who understand the purpose of your research. Whether you're building AI models, conducting observational studies, or planning a clinical trial, our platform gives you the data you need—ethically, transparently, and at scale.
Key Benefits
Larger, More Diverse Cohorts
Go beyond siloed hospital data. Access nationwide—and eventually global—data pools reflecting a broad range of demographics and conditions.
Lower Cost, Higher Efficiency
Reduce acquisition and legal overhead by working within a trusted, compliant framework. Build fit-for-purpose datasets instead of mining noisy EHRs.
Ethical, Transparent Data Use
Every data point comes with explicit, study-specific consent. Build trust in your research and improve the odds of regulatory and clinical adoption.
What You Can Do With ConsentHealth
Identify Target Cohorts
Search and filter by diagnosis, demographics, treatment history, and more.
Request Additional Data
Participants can be invited to share missing data, complete surveys, or upload lab results.
Engage With Participants
Provide updates, return results, or offer compensation—monetary or non-monetary—to boost participation and retention.
Recruit New Participants
Launch targeted campaigns with our platform or through our partnerships with advocacy organizations and health systems.
Built for Compliance and Interoperability
Our platform aligns with modern standards such as FHIR, LOINC, and RxNorm, ensuring smooth data integration and quality you can rely on. We adhere to HIPAA, GDPR, and other local regulations so you can stay focused on your research—not red tape.
Use Cases
AI Development for Rare Disease Diagnosis
Build a diverse training set with real-world variability and clean labels.
Post-Marketing Surveillance
Track long-term patient-reported outcomes for approved therapies.
Health Equity Research
Study underrepresented populations with data you can’t get from a single hospital system.
Ready To Collaborate?
Get in touch to discuss your project. Whether you need 500 participants with a rare mutation or 50,000 for a large-scale registry, we’re here to help you design a data collection plan that works.