Find eligible participants - with consent built in.
Researchers and clinical trial recruiters can securely identify and prescreen eligible participants using harmonized health records - always with patient knowledge and explicit opt-in. Datasolids operates within HIPAA and HITECH-aligned environments. We enable standardized data access that improves trial design, accelerates recruitment, improves healthcare outcomes, and strengthens funding proposals.
No records are shared without patient approval.
A cleaner operational path to recruitment.
Clinical trial recruitment
Quickly identify and prescreen participants using cooperative metadata - all with patient knowledge and consent.
Feasibility & cohort sizing
Validate inclusion criteria early and estimate volume before committing time or budget.
Research funding support
Use standardized formats and clean data to strengthen grant proposals, studies, and outcomes.
Designed for real-world trial operations.
Submit requirements
Define eligibility criteria, data needs, and study scope.
Cooperative discovery
Search anonymized cooperative metadata to estimate fit and volume.
Finalize terms
Agree on access terms and payout before any record sharing occurs.
Patient onboarding
Patients are invited and must explicitly opt in per study.
Questionnaires
Send follow-up questions to confirm eligibility or capture study inputs.
Payment
After the study is complete, participants receive payment.
Let's talk about your study.
If you're a research organization, university lab, or clinical trial recruiter looking to onboard onto our platform, get in touch.
Get in touch →