

Enrolment takes years. Participants disengage. Coordinators drown in admin. Promising therapies wait while paperwork stalls progress. Phase III delays cost $600K–$8M per day.
To talk to their own care team. GPs, specialists, allied health, mental health — all on different platforms. Messages get lost. The patient becomes the messenger. Care falls through the gaps.
"We built Flusso because clinical trials shouldn't be this hard — for anyone on either side."
AI extracts protocol arms, endpoints, eligibility from PDF in minutes — not weeks of manual entry.
Survey instruments and ePRO schedules push to participants as notifications — completed in under 3 minutes.
Retention dashboards and risk alerts deliver predictive flags before disengagement happens.
Multi-site coordination and audit trails provide real-time visibility across every site, simultaneously.
One app for GP, specialists, and their trial — no new download, no portal to forget. Their existing healthcare routine.
Surveys as smart notifications, not email attachments — feels native, part of their daily routine.
Plain-language consent — "Your heart rate data monitors medication safety." Transparency that builds trust.
Full visibility into who sees their data — trust through transparency is what turns 70% retention into 85%+.

Configurable protocol workflows with real-time amendment tracking and regulatory-grade audit trails from first patient in to database lock.
Multi-site coordination with performance dashboards, enrollment analytics, and decentralized trial support across geographies.
Electronic consent, patient-reported outcomes, and context-aware surveys that cut coordinator admin burden in half.
Participant-trial matching, dropout risk prediction, and automated protocol extraction — 15 operational AI features built in, not bolted on.
Trial discovery, gamification, and end-to-end encrypted messaging that directly attack the industry's 30% dropout problem.
Contextual Integrity embedded at every layer — compliant data collaboration by design, not by paperwork.
Built with Flutter for iOS and Android


Multiple organisations establish shared data norms once, then collaborate on every future request without renegotiating.
Built on a 20-year academic framework with 5,000+ citations — privacy violations aren't just flagged, they're architecturally impossible.
Data sharing agreements that take 18+ months today close in weeks, with every request evaluated against governance norms in milliseconds.
Publish, discover, and access governed data products with tiered pricing — turning cross-org data collaboration into a revenue stream.
HIPAA, GDPR, PIPL, and PDPA enforced through a single framework with immutable, regulator-ready audit trails.
Healthcare proves the architecture; mining, financial services, and government adopt proven infrastructure.
Perfect for cross-border trials, research networks, and pharma partnerships.

One secure inbox for patients and their care team. Surveys, messages, and reminders in the app they trust. Free for patients.
End-to-end clinical trial and study management. From protocol PDF to configured trial in minutes. Your AI-powered command center.
Collaborate on data across organizations without it ever leaving your systems. Agree on governance once—share forever.
GP, specialists, allied health, mental health — one encrypted thread per patient. No more faxes or phone tag.
Olm protocol. Keys on device only. Even Flusso can't read messages. No other clinical platform offers this.
Patients swipe through trials matched to their health profile. Recruitment happens where patients already are.
Apple Health, Fitbit, Oura data feeds eligibility screening and monitoring. Contextual consent for every flow.
Points, badges, streaks. Designed to drive survey completion rates above industry benchmarks by making participation feel rewarding, not burdensome.
Offline support, voice input, large text, 48px touch targets. Designed for the people most often left out.
Drop a PDF or DOCX. AI extracts arms, endpoints, eligibility, randomisation — with confidence scoring. You verify; you don't rebuild. Saves 2–4 weeks of setup.
ICH E6(R3) aligned. Arms, randomisation, objectives, endpoints, IRB tracking, site monitoring, protocol deviations — all in one platform.
Dedicated workflows for observational and longitudinal research. Not forced into trial workflows for non-interventional work.
Build once, deploy across any trial or study. Clone, version, share across your entire portfolio with zero duplication.
Eligibility pre-screening, diversity dashboards, wearable-based qualification. Patients matched and reached via Engage.
Bidirectional integration via Flusso Connect. Use both platforms without double entry. No disruption to existing workflows.
The root cause of complexity in managing clinical trials isn't technology. It isn't regulation. It's that current systems force an impossible choice: lock data down (killing innovation) or share freely (killing trust).
There has never been a middle ground — until now.
This is Contextual Integrity (CI)— a privacy framework developed over 20 years at Cornell Tech by Professor Helen Nissenbaum. Over 5,000 academic citations across law, computer science, and public policy. We turned it into production infrastructure.
Every data flow is validated against contextual norms before it happens.
Violations aren't against policy — they're technically impossible. The system itself prevents them. No policy gaps. No human errors. No misconfigured permissions.
Coalition members agree on sharing norms once. Every subsequent request is auto-validated. 80% pre-approved instantly. Legal friction eliminated by design.
Data stays in your systems. Only governance rules flow between organisations. Zero breach liability — because there is no data processing.
Define activities, attributes, subjects, roles, norms, and transmission principles. Visual configuration — not legal documents.
Register, tag, version, and publish data assets. Access requests with governance evaluation. Organisations earn revenue from their data contributions.
Automated classification per context — the same data may be sensitive in one context and entirely appropriate in another. Context-aware, not field-locked.
HIPAA, GDPR, PDPA, PIPL built in. Regulatory changes become configuration updates, not architecture rebuilds.
Governance that travels. Data that doesn't. Your legal team will approve sharing on this platform that they'd never greenlight anywhere else — because violations are architecturally impossible, not just against policy.
Five hospitals. Twelve patients each — nowhere near statistical significance alone. With Data Coalitions, they form a governed research network in weeks, not years. Participants are already on Engage. Trial workflows run through Participate. Combined cohorts of hundreds. No new legal agreements. The research that was impossible last year becomes routine this year.
A network of 200 GP practices joins a Data Coalition. Patients use Engage for care coordination. When a pharmaceutical company needs a diabetes cohort, coalition governance norms pre-approve the query. Eligible patients are surfaced through Engage with contextual consent. GPs refer in minutes, not weeks. Practices earn marketplace revenue.
A trial spans Australia, Singapore, and Hong Kong. Each jurisdiction has different privacy laws. Participate manages the protocol. Engage keeps participants connected. Data Coalitions handle cross-border governance with CI norms that satisfy all three regulatory regimes simultaneously. Global trial data that actually globalises.
End-to-end encryption via Olm protocol. Keys on device only. Flusso cannot read patient messages — by design, not by policy. No other clinical platform offers this level of security.
82+ database tables implementing the CI framework. Three-tier governance evaluation engine. Violations aren't just against policy — they're architecturally impossible.
HIPAA, GDPR, PDPA, PIPL, NHMRC, ICH E6(R3), 21 CFR Part 11. Cross-border compliance built into the architecture. Regulation changes = configuration updates, not code changes.
Every data access, consent decision, and governance evaluation — permanently logged. Ethics committee audits take hours, not weeks. NHMRC-compliant reports exportable on demand.
PDF to configured trial with confidence scoring. Minutes, not weeks of manual setup.
Flag participants at risk of disengaging before they leave. Intervene early, retain more.
Accelerate eligibility assessment. Surface promising candidates, flag exclusions automatically.
Catch deviations automatically. Real-time compliance monitoring across every site.
AI matching surfaces relevant trials based on health profile, location, and preferences.
Reminders and content that adapt to individual preferences and schedules. Right time, right channel.
Automatically classify data sensitivity per context, not per field — the CI way.
Surface compatible datasets and mutually beneficial partnerships across the coalition network.
If your most pressing challenge is your next clinical trial — protocol setup, enrolment, or retention.
If your priority is care coordination across a provider network or improving participant communication.
If multi-site data collaboration or cross-organisational research is your most immediate bottleneck.
Three products. One governance layer. The platform that solves healthcare's trust problem — so patients complete trials, providers coordinate care, and organisations collaborate on research that was previously impossible.
30 minutes. Tailored to your organisation's specific challenges — not a canned demo. We come prepared with your workflows in mind.
Explore product details, case studies, and the Contextual Integrity framework behind the platform.
Email us at contact@flusso.ai​ and we will respond within one business day with a proposed agenda tailored to your team.
The complete trial platform