Healthcare data for model development

We work with data partners to qualify clinical and multimodal cohorts for post-training and evaluation, with the histories, tasks and evidence the research needs.

Luminous mineral lamellae.

Hundreds of clinical-history environments

We build each environment from partner records after checking chronology, linkage and missing context, then run it against frontier models. Clinicians shape the rubrics.

Clinical and multimodal data

Clinical histories

Encounter notes, treatments, diagnoses and follow-up records, with chronology and source references.

Imaging & pathology

Radiology studies, associated reports and digital pathology, with image-to-record linkage checked for each study.

Laboratory & molecular data

Lab observations, sequencing and molecular measurements, linked to the patient record.

Longitudinal cohorts

Records across visits and modalities, scoped around a research question.

Each task starts at a fixed point in the patient history

Future events stay out of the input. Each expected response has a rubric, evidence requirements and clinician review.

For extraction tasks, the model identifies a documented event, keeps its date and returns the supporting source span.

Inside a clinical environment

Patient history up to the task start

  1. Clinic visit
  2. Lab result, abnormal
  3. Medication started
  4. Imaging
  5. Clinic visit
  6. Task starts here
  7. Later events, hidden from the model

Care plan from the model

  • MedicationChange, dose and reason
  • Follow-upTest and timing
  • ReferralSpecialty and urgency

Rubric from clinicians

  • Acts on the abnormal resultCritical
  • Avoids a known interactionCritical
  • Sets follow-up timingImportant
  • Cites evidence from the historyImportant

PassEvery critical item met, 3 of 4 overall

What each dataset includes

Cohort qualification

Population, time period, modalities, inclusion criteria and completeness, with gaps recorded alongside the coverage.

Rights and provenance

Source authority, permitted purpose and onward-use conditions, with source and delivery records kept connected.

Task and review design

The input boundary, reference evidence and evaluation rule for each task. Clinicians review the rubrics.

Delivery

Schema, formats and access path agreed with the receiving team. Raw source data and prepared training tasks ship separately.

Work with us

Tell us what the work is, what data it touches and what constraints apply. We’ll work out what to build and how to measure it.