About our platform- Landing Page
One governed infrastructure. Every layer of the evidence stack.
Celéri Health builds and operates the data backbone that connects point-of-care outcomes, sponsored commercial registries, regulatory-grade real-world evidence, and a large de-identified pain dataset — on the same patients, without starting over.
From the first patient scan to a peer-reviewed manuscript.
Each layer feeds the next. Data captured at the point of care becomes sponsored evidence, sponsored evidence becomes regulatory-grade evidence, and every governed record strengthens the benchmark dataset behind it all.
Enrollment & outcomes capture
Celéri EaaS™ Platform
PainRWD™ Science Cloud
Evidence in the hands of the people who use it
Evidence infrastructure. Not just a registry.
Most evidence programs are built once, for one purpose, and abandoned when the study ends. Celéri Health builds permanent evidence infrastructure — platforms that generate commercial intelligence today and regulatory-grade data tomorrow, on the same patients.
One platform. Two functions. No rebuild.
Commercial and medical affairs teams draw from the same governed dataset — physician-level outcomes for the field, publication-ready longitudinal data for medical. No duplicate infrastructure. No version conflict.
Built regulatory-ready.
Every sponsored engagement runs on infrastructure purpose-built for 21 CFR Part 11 and governed under HIPAA. When signals confirm the right indication, the evidence base is designed to transition into a regulatory-grade cohort — same patients, no data migration.
Point of care to publication.
Practice registry, sponsored commercial program, regulatory submission, and journal publication — one connected infrastructure spans the full evidence lifecycle.
Four products. One evidence lifecycle.
Each product stands on its own. Together they connect a physician's first patient encounter to the evidence a sponsor, a payer, or a journal needs.
Celéri EaaS™ Platform
End-to-end Evidence-as-a-Service™ for medtech and pharma sponsors. Commercial Insights Registry™, Regulatory-Grade Evidence Cohort™, and traditional prospective study — one governed infrastructure, three evidence tiers. Deploy a governed real-world evidence registry in roughly eight weeks, at sponsors' own existing accounts.
Explore the EaaS™ Platform ›PainIntel™
Practice-level registry and outcomes platform for interventional pain physicians. 30+ validated PRO instruments, EHR integrations, automated patient outreach, and a real-time Pain Command Center — with no added staff burden. Your practice, your registry, your evidence.
Explore PainIntel™ ›PainRWD™ Science Cloud
A large de-identified longitudinal real-world pain dataset — PROs, procedures, diagnoses, and utilization signals — with ZIP-level social determinants enrichment. Used for external control groups, HEOR modeling, payer dossiers, and benchmarking sponsor evidence.
Explore PainRWD™ Science Cloud ›myPainIntel™
Patient-facing mobile app for PRO check-ins, visual pain tracking, and longitudinal outcomes monitoring. Deploy it out of the box or white-label it under a sponsor's brand. Improves completion and long-term follow-through in both practice and sponsored registry settings.
Explore myPainIntel™ ›Two environments. One data model.
Practice-side and sponsor-side evidence run in separate, separately governed environments that share a common data model — so a physician's registry and a sponsor's program never compromise each other, and evidence can move up the stack when consent and governance allow.
Point-of-care outcomes
Built for clinical workflow and practice-owned evidence. Physicians capture outcomes on every encounter and see them in real time.
- PainIntel™ practice registry and Pain Command Center
- myPainIntel™ patient app
- EHR integrations at no cost to the practice
- Investigator-initiated study support through the Celéri Research Group
Purpose-built for 21 CFR Part 11
The default for every medtech and pharma EaaS™ engagement — because audit trails cannot be applied retroactively. Commercial from day one, regulatory-ready from enrollment.
- Commercial Insights Registry™ — always running from launch
- Regulatory-Grade Evidence Cohort™ — sequential or parallel, on the same patients
- Tiered eConsent, IRB-ready protocol scaffolding, proprietary in-house EDC
- Separately governed and separately funded from any concurrent clinical study at the same site
What every product runs on.
Ready to build your evidence infrastructure?
Whether you're a medtech sponsor at commercial launch, a pain physician building a practice registry, or a payer looking for comparative effectiveness data — Celéri Health has an evidence pathway for you.
