Community-Powered Research. Real-World Results.
Clinical research moves faster when communities lead.
We connect sponsors to diverse, informed participants through a HIPAA-compliant registry powered by crowdsourced insight—so recruitment is faster, retention stronger, and trust built in.
Why It Works
Crowdsourced Feedback → Better Messaging
We ask real people what matters to them—then co-create outreach that converts interest into action.
Data-Driven Precision → Smarter Targeting
Geo-data + SDOH analytics identify where to engage and how to support participants long-term.
Community Trust → Sustainable Enrollment
Local ambassadors deliver plain-language education and warm handoffs to study sites.
The Curated Clinical Advantage
IRB-approved, privacy-protected registry
Opt-in participants ready to learn about trials
Real-time feedback on message and retention
Measurable increases in minority representation
Sponsors partnering with Curated Clinical see:
Let’s Build Equitable Research Together
Every data point starts with a person.
Partner with Curated Clinical to make clinical trials more inclusive, efficient, and human.
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