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For Clinical Research

Clinical trials that work for everyone

Manage multi-site clinical trials with unprecedented efficiency, participant retention, and regulatory compliance.

Built for modern clinical research

Powerful tools that streamline every aspect of trial management

Patient-centric trial configuration

Design trials that put participants first. Intuitive interfaces make complex protocols accessible.

Multi-site coordination

Manage trials across multiple sites with centralized oversight and real-time visibility.

Automated data collection

Capture patient-reported outcomes, surveys, and clinical data automatically with smart scheduling.

Real-time participant engagement

Keep participants informed and engaged with personalized communication and progress tracking.

Regulatory documentation

Generate compliant documentation automatically. ICF, IRB submissions, and protocol amendments made easy.

Comprehensive audit trails

Every action is logged and timestamped. Meet regulatory requirements with confidence.

Built-In Intelligence

Operational Intelligence That Outpaces the Competition

While competitors like Medidata and Veeva focus on data management, Flusso delivers AI-powered insights that help your site run more efficiently and retain more participants.

AI-Powered Pre-Screening

Parse complex eligibility criteria automatically. Get eligibility scores in seconds, not days.

Faster screening

Dropout Risk Alerts

Identify at-risk participants weeks before they disengage. Intervene early, retain more.

Higher retention

Protocol Variance Detection

Catches site drift before it impacts data quality. Real-time monitoring across all sites.

Real-time compliance

Competitive Trial Analysis

See how your trial compares. Track competing enrollment, analyze therapeutic landscape.

Market intelligence

Your Data Stays Protected

All smart features are built on our Contextual Integrity framework. Your participants' data is never used to train models, and every recommendation can be explained.

HIPAA Compliant No Data Training Explainable Results

From protocol to publication, simplified

Three steps to transform your clinical trial operations

1

Configure your trial protocol in minutes

Use our intuitive builder to set up visit schedules, activities, and data collection requirements.

2

Enroll and engage participants seamlessly

Streamlined consent process, automated reminders, and personalized participant portals.

3

Generate compliance documentation automatically

Export audit-ready reports, track protocol deviations, and maintain regulatory compliance effortlessly.

The Patient Experience

What your participants actually see

Everything you configure in Participate, participants experience through Engage—their trusted healthcare app.

The participant journey

Week 0 Enrollment
  • Consent form appears in Engage
  • Welcome message from research team
  • First visit reminder scheduled
Week 2 First Study Visit
  • 24-hour reminder notification
  • Day-of confirmation request
  • Post-visit thank you + next steps
Week 4 Survey Window
  • ePRO notification with estimated time
  • Simple tap-to-start interface
  • Completion confirmation + appreciation
Ongoing Engagement
  • Protocol updates and announcements
  • Community access (if enabled)
  • Progress milestones and encouragement

They're not downloading "another trial app"

The #1 adoption barrier in clinical trials is asking participants to download and remember yet another app. With Flusso, your trial lives inside Engage—the app they already use for their GP, specialists, and health records. No friction, no forgotten logins, no app fatigue.

What you see when they engage

When participants...
You see in Participate
Open a survey notification
Real-time completion tracking
Read a message
Read receipt + timestamp
Confirm a visit
Attendance prediction update
Engage less frequently
Dropout risk alert

Built for Clinical Research Coordinators & Investigators

Trials that run themselves

Spend less time on administration, more time on science

High participant dropout rates due to poor engagement

Intelligent engagement tools that keep participants connected and motivated

Manual data entry consuming coordinator time

Automated data collection directly from participants and integrated systems

Fragmented systems requiring multiple logins

Single platform for all trial management activities

Compliance documentation taking weeks to prepare

One-click generation of audit-ready regulatory documentation

Limited visibility into multi-site trial progress

Real-time dashboards showing enrollment, retention, and data quality across all sites

Ready to revolutionize your clinical trials?

Join research institutions that are achieving higher retention rates and faster enrollment.

Talk to our team to see how Flusso can transform your operations.