Healthcare & MedTech

Clinical AI that a clinician signs before it acts.

Large clinical-ops opportunity, longer procurement cycles, and a liability line most firms won't touch. We serve payer operations, provider systems, and MedTech device companies — including a hardware-plus-software due diligence capability no software-only consultant can offer.

Payer OperationsProvider SystemsMedTech DevicesPE / VC MedTech Diligence

Use Cases

Eight use cases, from clinical ops to the device layer.

Use caseTechniqueValue delivered
Clinical documentation automationFull fine-tune on SOAP notes60–70% less documentation time
Discharge summary generationQLoRA on EHR recordsStandardised, audit-ready summaries in minutes
Prior authorisation processingRAG on payer policy docs80% faster PA turnaround
Medical coding (ICD-10 / CPT)Full fine-tune on clinical docs90%+ auto-coding accuracy
Diagnostic decision supportFull fine-tune on clinical literatureTriage-level diagnostic confidence at point of care
Radiology report draftingFine-tune on radiologist corpusDraft report in seconds; radiologist edits and signs
Clinical trial matchingRAG on eligibility criteria10x faster eligible-patient ID
MedTech DD — BLE hardware layerOperator-level firmware assessmentUncovers device risks software-only consultants miss

The Boundary

Clinical AI Track A / Track B — a published protocol.

The liability cliff isn't clinical AI itself — it's clinical AI autonomy. A supervised POC that a clinician reviews before acting is fundamentally different from a model that makes autonomous treatment decisions. Track B captures the revenue without the catastrophic-risk scenario.

Track A — Non-Clinical

Full delivery

Banking, retail, enterprise SaaS, non-clinical healthcare operations, PE ops. Production code, model fine-tuning, deployment — no restrictions.

  • Standard SOW and IP Firewall
  • Full implementation team
Track B — Clinical

Safeguarded trial delivery only

Sandbox / POC / validation environments. Human Review clause mandatory in every SOW. Clinical Governance Acknowledgement (CGA) required. PHI stays in your tenant, always.

  • We review; your clinical team validates
  • Never autonomous — a clinician is always in the decision loop

For PE & VC

Diligencing a MedTech target? See what software-only reviews miss.

Hardware-plus-cloud due diligence in one engagement — the seam between device and model is where MedTech investments actually fail.

Explore MedTech Due Diligence