Encounters
Diagnoses · procedures · care pathways
The trusted network for Real-World clinical data
First-Party.Direct From Source.Live. Longitudinal.Multimodal.
Patient-level clinical data connected across encounters, records, notes, labs, devices, therapies and diagnostics—continuously refreshed from U.S. providers.
ONMDSource profileDirect from source
- 0M+
- Patients
- 0+
- U.S. facilities
- 100%
- Direct sourced
- DAILY
- Refresh
FIRST-PARTYDIRECT FROM SOURCELIVELONGITUDINALMULTIMODALOMOP 5.4DAILY REFRESHHIPAA SAFE HARBORHEALTHVERITY + DATAVANTFIRST-PARTYDIRECT FROM SOURCELIVELONGITUDINALMULTIMODALOMOP 5.4DAILY REFRESHHIPAA SAFE HARBORHEALTHVERITY + DATAVANT
01 / The data
One living patient index. Every clinical dimension.
First-party data remains connected to its source, preserving provenance while new clinical activity extends each longitudinal record.
Clinical records
Structured EMR · unstructured notes
Diagnostics
Laboratory results · reports · imaging
Device signals
ECG · EEG · waveforms · interpretations
Therapies
Medication · utilization · adherence
Patient-reported
Outcomes · symptoms · quality of life
First-party
Provenance
Direct
Source relationship
Daily
Refresh cadence
Longitudinal
Patient history
Multimodal
Clinical breadth
02 / For life sciences
A better foundation for Real-World Evidence.
Multimodal, longitudinal, patient-level data reveals the clinical signal that claims and single-source records leave behind.
EHR + EMR
Encounters, diagnoses, procedures, medications and the full care journey.
Clinical notes
Provider, surgical and discharge narratives that reveal signals structured fields miss.
Imaging
Native studies, reports, findings and diagnostic metadata linked at patient level.
Laboratory
Chemistry, hematology, pathology and genetic results connected to longitudinal history.
Device data
ECG and EEG waveforms paired with interpretations and associated clinical context.
Pharmaceutical
Prescription history, utilization and adherence connected to Real-World outcomes.
From query to evidence
Explore before you license.
Confirm cohort depth, coverage, field availability and quality before committing. Then receive only the matched patients and attributes your study requires, in an analytics-ready structure.
RWE + HEOR
Outcomes and safety
Synthetic controls
Trial acceleration
Payer evidence
Defensible endpoints
Living cohorts
Scheduled refreshes
03 / Fit-for-purpose curation
We are a curation partner. Not a data reseller.
A named delivery team builds every engagement around your study question, label schema and regulatory pathway.
- 01
Define
Study question, indication, inclusion criteria and endpoints become a written specification.
- 02
Feasibility
Counts and volume are confirmed with your team before contract signature.
- 03
Sample
A representative sample arrives in your target format for hands-on review.
- 04
Refine
Schema, labels and cohort are tuned against your feedback.
- 05
Scale
The accepted spec becomes a full build with QC and provenance per record.
Dedicated project manager
One accountable lead for scope, schedule, change requests, refreshes and follow-on work.
Curation specialist
Clinical intent translated into query logic, cohort definitions and a delivery schema that answers the question asked.
04 / Privacy by construction
De-identification is the first step. Not the last.
HIPAA Safe Harbor is the baseline. Expert Determination is available when a use case requires it, with redaction confined to the PHI bounding box.
At-source De-ID
Headers, free text and burned-in pixels checked across four detection technologies.
Evidence: Per-record pass log
Human-in-the-loop QC
Manual review confirms no residual PHI before data reaches the cohort library.
Evidence: Batch QC sign-off
Clinical expert audit
Pixel-level diagnostic integrity with no recompression, depth reduction or re-windowing.
Evidence: Reviewer attestation
Conformance to spec
Completeness, linkage, coding normalization and delivery schema verified.
Evidence: Acceptance audit trail
HITRUST certified
SOC 2 Type II
AES-256 encryption
Role-based access
05 / Programs supported
Built for the evidence standard ahead.
Delivered as native DICOM with CSV, SAS, Parquet or JSON companions — one-time or on a scheduled refresh.
Foundation models & AI training
Multimodal pre-training and ground-truth datasets across clinical records, diagnostics, notes, labs and device signals, with source provenance and longitudinal context.
Device validation
510(k) and PMA evidence with provenance attached to every accepted record.
Post-market surveillance
Live, longitudinal Real-World Data to monitor safety, performance and outcomes after approval.
In market / July 2026
$11.5M+
Initial contract value
Foundation-model scale is already in motion.
An initial agreement to supply millions of de-identified, multimodal clinical records for development and training of a foundational AI model.
Next step / 30–45 minutes
Start with the cohort you need.
Walk through your criteria, confirm the depth and volume available, and meet the team who would run the engagement.
Request a working sessionNO OBLIGATION · CURATED TO YOUR SPEC