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Vokl
  • Platform
  • PATIENTS
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  • About
    • Articles
    • Contact Us
    • FAQ
    • Trust
    • Values

Convert Patient Consent into Clinical Velocity

Stop Buying Static Snapshots. Access LivinG Evidence.

De-Risk Your Pipeline with High-Fidelity Retention

Protect Exclusivity Revenue

Compress trial timelines by front-loading patient engagement. Every day saved in clinical development protects $600K–$8M in patient exclusivity revenue

Longitudinal, Regulatory-Grade Evidence

Go beyond clinical endpoints. Capture longitudinal RWD on quality of life, symptom burden, and treatment adherence directly from verified patient communities

FDA-Aligned Diversity Access

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

Eradicate Preventable Dropouts

Keep patients engaged through 'Retention by Design.' By incorporating Patient Burden Scoring into protocol design, we prevent screen failures and dropouts before they happen

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Patients need to be in charge of their own data, and that means determining how to use and potentially profit from those data - We owe this to patients.


Ravi B. Parikh, MD - Coalition to Transform Advanced Care

Consent-Driven Pipelines at Scale

Build community-driven data pipelines to replace one-off outreach - Condition communities opt-in together accelerating recruitment 3×

Community-Validated Eligibility

Condition communities validate eligibility logic - real-world feedback improves computable criteria and reduces false exclusions to cut screen failures by 40%

Retention by Design

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

Hybrid Access with Community Infrastructure

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

Build Trust + Regulatory Confidence

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

What is Living Evidence?

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

Curious to learn more?

Schedule a consultation today and take the first step towards accelerating your clinical velocity

Request A Consult
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