Compress trial timelines by front-loading patient engagement. Every day saved in clinical development protects $600K–$8M in patient exclusivity revenue
Go beyond clinical endpoints. Capture longitudinal RWD on quality of life, symptom burden, and treatment adherence directly from verified patient communities
Move from transactional data buying to sustainable partnerships that satisfy FDA Diversity Action Plan mandates. Our transparent compensation models ensure GDPR & HIPAA-compliant access to re-contactable patient pools
Keep patients engaged through 'Retention by Design.' By incorporating Patient Burden Scoring into protocol design, we prevent screen failures and dropouts before they happen
Ravi B. Parikh, MD - Coalition to Transform Advanced Care


Cut trial attrition by 30% - retention improves when patients co-design trial experiences - community insights inform scheduling, burden scoring, and caregiver support

Bring trials to patients, not the reverse - Communities help map access barriers - Geo-mapped burden scoring improves site selection and hybrid trial feasibility

De-identifiable community data sharing + consent and compensation models build trust - and meet CT.gov, CTIS, and DAP requirements

Living Evidence is real-time, longitudinal patient data that evolves beyond static clinical snapshots. Unlike traditional EHR data, Hyper-Care's Living Evidence utilizes Patient Burden Scoring and zero-party consent to reduce screen failures and satisfy FDA Diversity Action Plan requirements
Schedule a consultation today and take the first step towards accelerating your clinical velocity