Evidence-as-a-Service — Celéri Health
Evidence-as-a-Service Platform

Enroll patients. Generate evidence. Built regulatory-ready.

Two ways to bring patients into the platform. One governed infrastructure behind both. Start with commercial intelligence — real-time outcomes for your sales and medical affairs teams. Activate regulatory-grade evidence whenever you're ready, on the same patients, with no rebuild.

57%
Mean NRS pain reduction at 90 days*
82%
30-day assessment completion rate*
8 wks
Time to a fully operational platform
85%
Cost reduction vs. traditional study

*Illustrative sample signals from a commercial engagement (182 patients, 16 sites) — the kind of signal the platform surfaces as a cohort matures, not a population-level claim.

Enrollment Pathways

Two ways in. One platform.

Choose the enrollment path that fits your commercial model — or run both. Every patient enters the same governed, HIPAA-compliant infrastructure regardless of how they arrive.

Primary Path · Direct-to-Patient

QR Code Direct-to-Celéri

Place a QR code on product packaging, patient discharge materials, trifolds, or demo kits. Patients scan and enroll directly — no rep account setup, no portal complexity, no site staff required.

  • Patient scans QR code on packaging, brochure, or sales collateral
  • Chooses App Path (custom-branded app or integration with an existing app) or Direct Enroll (mobile form, app optional later)
  • Every patient enters the same Part 11-ready, HIPAA-compliant platform — eConsent captured digitally against governed registry infrastructure
  • Automated PRO sequences begin immediately — NRS, PGIC, PROMIS-29, ODI at defined milestones
  • Data flows to the sponsor Command Center in real time — no rep action required
Brand flexibility: Deploy under your brand as a fully white-labeled experience, or use myPainIntel™ as your out-of-the-box patient engagement channel.
Enterprise Path · Rep-Initiated

CRM-Integrated Enrollment

For commercial organizations that want enrollment embedded directly in the rep workflow. Reps submit patients to the registry from within your existing CRM — no duplicate entry, no separate portal, no change to the pre-procedure process.

  • Rep submits patient record from CRM at the pre-procedure stage
  • Celéri receives the enrollment trigger — patient outreach begins automatically
  • Every patient enters the same Part 11-ready, HIPAA-compliant platform — eConsent delivered via SMS or email, no site visit required
  • Rep gets enrollment confirmation and milestone alerts back through the CRM
  • Patient outcomes surface in the rep territory view in real time
Used in our case study engagement: This client's sales team submitted patients from their CRM as part of standard pre-procedure workflow — achieving 82% 30-day completion with no duplicate data entry.
Platform Flow

Enroll. Engage. Signal. Act.

Four steps from patient enrollment to clinical decision — fully automated, no site staff burden.

01

Enroll

Patient enters via QR scan or CRM trigger. eConsent captured digitally. Tiered consent built in — commercial feedback, registry participation, or both.

Part 11-readyeConsentHIPAA
02

Engage

Automated SMS and email sequences deliver PRO assessments at baseline and every clinical milestone. Behaviorally-informed messaging maximizes response.

NRS · PGICPROMIS-29ODIPain Body Map
03

Signal

Outcomes surface in real time — rep territory views, physician-level performance, indication and payer signal analysis. Benchmarked against PainRWD™ comparator data.

Live Command CenterMCID AlertsBenchmarking
04

Act

Commercial teams use outcomes in physician conversations. Medical affairs uses the same dataset for publication and payer submissions. When ready, activate the Regulatory-Grade Evidence Cohort™ — same patients, no rebuild.

Field ActivationPayer DossierPublication
Evidence Architecture

The regulatory pathway, preserved from enrollment.

The Commercial Insights Registry™ is always Layer 1 — it runs from launch and never stops. The Regulatory-Grade Evidence Cohort™ runs on top of it. Start both together, or add regulatory-grade evidence when your signals tell you it's time.

Layer 1 · Commercial Insights Registry™ — always runningNOW
Path A · Sequential

Commercial signals build first. Add the Regulatory-Grade Evidence Cohort™ later, on the same patients.

Path B · Parallel

Regulatory-Grade Evidence Cohort™ runs alongside the commercial registry from launch.

Layer 1 is always the foundation — the Regulatory-Grade Cohort runs on top of it, whenever it starts.

Every commercial engagement preserves the regulatory pathway.

Celéri's infrastructure is designed to be 21 CFR Part 11-ready and IRB-ready from enrollment — even in pure commercial mode. That means when your signals confirm the right indication, payer segment, or geography, your evidence base is built to transition into a regulatory-grade cohort — without new infrastructure or data migration. Whether the goal is payer coverage expansion, label update, or peer-reviewed publication, the foundation is already in place.

Commercial + Medical Affairs

One dataset. Two teams. No version conflict.

The most expensive data in medtech is data that has to be gathered twice. Celéri gives commercial and medical affairs access to the same governed evidence base — each with the view built for their function. One governed, HIPAA-compliant data environment; one source of truth.

Commercial Team

Real-time outcomes intelligence

  • Rep territory view: case volume, NRS trends, milestone alerts, open follow-ups
  • Physician-level outcomes — blinded patient results, available in a clinical conversation
  • Signal analysis by indication, payer type, and geography — no data analyst required
  • MCID breach alerts routed to the assigned rep automatically
  • Site FMV eligibility tracking for the Commercial Insights Program
Medical Affairs

Publication-grade evidence pathway

  • Same governed cohort — draws from identical data, not a parallel extract
  • Signal analysis drives cohort scoping before protocol design begins
  • Longitudinal PRO dataset: NRS, PROMIS-29, ODI, PGIC, procedure timelines
  • Payer dossier and HEOR modeling via PainRWD™ Science Cloud comparator data
  • Celéri Research Group available for biostatistics review and manuscript support
The Command Center

Four views. One governed environment.

Every tab draws from the same HIPAA-compliant data infrastructure — access-controlled by role. The figures shown are illustrative sample signals — the kind of evidence Signal Analysis surfaces as a cohort matures.

celéri health 90-Day Snapshot Signal Analysis Rep & Physicians Reconciliation ILLUSTRATIVE Mean NRS — signal building over 90 days Client cohort vs. PainRWD™ benchmark · lower is better 86420 NRS (0–10) Signal: ≈57% mean reduction* Baseline2w4w6w30d60d90d Client cohort PainRWD™ benchmark −3.9 Δ Mean NRS · baseline → 90 days ≈57%* Mean NRS reduction (illustrative) PGIC at 90 days 77% better Very much (34%) Much (43%) Minimal (15%) No change (8%) *Illustrative sample signal · n=182 across 16 sites · updates in real time

Sample Command Center — Signal Analysis view. Illustrative signals, not a population-level claim.

90-Day Snapshot

Cohort KPIs anchored to procedure date

The primary leadership view. NRS trajectory, PGIC distribution, enrollment trends, and 30-day completion — in a single view updated in real time. 24+ KPIs available, including PROMIS-29, NRS, PGIC, EQ-5D, ODI, and custom instruments per indication.

  • NRS Trajectory — mean pain by timepoint, baseline through 90 days, benchmarked to PainRWD™
  • PGIC Distribution — patient-centric outcomes narrative for health-system and payer conversations
  • Enrollment Trend — monthly growth by site; tracks rep engagement and site maturation
57%
NRS reduction, 90 days
77%
PGIC much/very much better
182
Patients · 16 sites
Signal Analysis

Outcomes by indication, payer, and geography

Lets clinical and market-access teams interrogate outcomes without a data analyst — and doubles as the scoping instrument for the Regulatory-Grade Evidence Cohort™, confirming the optimal indication, payer segment, and geographic cohort before protocol design.

  • Indication Signal — case volume and NRS improvement by indication
  • Payer Signal — outcomes by payer type for market-access discussions
  • Geographic Performance — volume and NRS improvement by state
4.2
Avg NRS improvement, top indication
4.3
NRS improvement, commercial payer
5
Indication categories
Rep & Physicians

Close the loop between activity and outcomes

Commercial leadership sees, in a single governed view, which reps drive enrollment, which physicians deliver the strongest outcomes, and which patients are overdue. The physician-outcomes view is sales-enablement safe — reps filter to a physician's cohort with patient identities blinded.

  • Rep Performance — cases enrolled vs. 30-day completion by rep
  • Physician Outcomes — top physicians by volume and average NRS improvement
  • Milestone Tracking — patients pending or overdue, for proactive outreach
89%
Completion, top reps
4.1+
Avg NRS, top physicians
Blinded
Identities in rep view
Reconciliation · Restricted

Site FMV eligibility — admin view

Tracks milestone completion across enrolled patients to determine site eligibility for Fair Market Value payments in exchange for Commercial Insights Program participation. Access-controlled to authorized client and Celéri admin only — Celéri surfaces eligibility; dollar amounts and disbursement stay in your finance workflow.

  • Site Eligibility Summary — sites meeting milestone thresholds this period
  • Milestone Completion Funnel — attrition from consent through 90-day completion
  • Access Controlled — restricted read-only; not accessible to the field team
87.5%
Sites eligible this period
95%
Consented completing baseline
Admin
Not visible to field
Trusted By

Leading MedTech & Pharma sponsors.

PainTEQ Medtronic Interaxon Ethos CornerLoc Aurora Spine

Talk to a Celéri strategist.

We'll help you identify the right enrollment path and evidence tier for your product and commercial stage — whether you're at launch or seeking evidence renewal for a mature product line.

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