Real-world evidence platform

    Launch Your Study in Under 48 Hours.

    Once your protocol and ethical approval are ready, Aria handles the rest. We automate the entire participant journey—from smartphone onboarding to real-time data tracking. The fastest route to regulatory-grade evidence.

    Get My Study Blueprint

    Takes 5 minutes • Generated by our Clinical Engine + Expert Review • Delivered within 24 hours

    Built for

    Supplement & Nutraceutical
    Health Innovators
    Patient Organisations
    Research Institutes

    Vetted & Partnered with

    EIT HealthEuropean Innovation CouncilThe LancetNovartis BiomeGerman Medical InstituteForbes

    Why spend 6 months on setup when you can launch this week?

    The Old Way

    Slow, fragmented, expensive.

    • 6 months of setup
    • Multiple disconnected tools
    • Wait-and-see data
    • High participant dropout
    The Aria Way

    Rigorous, automated, fast.

    • Study live in 48 hours

      From protocol to live study in under two days.

    • One unified study flow

      Single platform for engagement and oversight.

    • Real-time visibility

      Track progress and catch issues as they happen.

    • Higher participant completion and adherence

      Better engagement means better data quality.

    One platform for participant engagement and study oversight.

    Participant Application

    • ePRO and Survey Delivery
    • AE and Symptoms Capture
    • Medication Adherence Tracking
    • Task Management and Notifications
    • Rewards and Engagement Logic
    • One-Way Participant Communication

    Research Platform

    Aria Research Platform
    • Rapid Study Setup
    • Real-Time Progress Tracking
    • Digital eConsent
    • Smart Scheduling
    • Regulatory-Grade Data Handling
    • Direct Community Invitations

    Data Infrastructure

    AWS-hosted secure cloud environment
    Live mobile-to-platform data synchronization
    GDPR-compliant data architecture
    Externally assessed security controls
    The Process

    From Protocol to Participant.

    01

    Protocol & Blueprinting

    Submit your goals. Our experts review your study design and finalize a digital protocol optimized for the Aria engine.

    02

    Ethical Submission Pack

    Generate the documentation you need for IRB/Ethics approval: Participant Information Leaflets, Consent Forms, and Data Safety Plans.

    03

    Platform Build & Validation

    While your ethics review is pending, we configure your study environment. Run internal tests to ensure your surveys and triggers are perfect.

    04

    Community Onboarding

    Once approved, deploy your unique study link to your patients, community, or recruitment partners. One-click onboarding starts the data flow instantly.

    Ready to launch your study?

    Stop the manual grind. Let our Roadmap Engine build your first study protocol draft and identify key clinical considerations for free—providing a rigorous, validated foundation for you to finalize and launch.

    Get My Study Blueprint

    Generated by our Roadmap Engine • Delivered to your inbox within 24 hours

    Study Protocol already finalized? Get in touch and let's get started.

    Trusted by EU-backed research teams and international medical institutes.