Clinical documentation infrastructure

AI drafts the report. A clinician signs it.

Med-AI Clinical prepares structured radiology and laboratory reports from studies your hospital already produces. Every draft goes to a licensed practitioner, who edits and signs it. Nothing reaches a patient record unsigned.

Become a design partner Selecting two hospitals for paid pilots.

Draft, review, sign

The workflow radiologists already use, with the first pass prepared for them. The signature is enforced by the software, not asserted in a policy document.

01

A study arrives

An image or lab report is uploaded, or arrives from your existing systems. It is analysed and a structured draft is prepared — findings, impression, coded conclusions.

02

A clinician reviews

The draft appears on a reading worklist, oldest first. The reviewer accepts it, corrects it, or rejects it with a reason. Urgent findings are escalated separately until somebody acknowledges them.

03

The report is signed

Signing attributes the report to a named practitioner with a timestamp. Only then does it become final — including to any system reading it over FHIR.

Built for the parts nobody demos

Most of the work in clinical software is not the model. It is isolation, auditability, consent and interoperability — the questions a hospital's IT review asks first.

Tenant isolation in the database

Each hospital's data is separated by PostgreSQL row-level security, not only by application code. A missing filter in a query cannot leak another hospital's records.

An audit trail that cannot be rewritten

Every read and write is recorded. The application can append to the audit log and cannot alter or delete it. Six-year retention is enforced in the database.

FHIR R4 interoperability

Patients, observations, diagnostic reports and imaging studies are exposed as conformant FHIR R4 — the same standard India's ABDM is built on.

Coded, validated output

ICD-10 conclusions and LOINC-coded lab results. A code the system cannot confirm is carried as text rather than asserted as a coding.

Prescription safety checks

Drug-class allergy cross-reactivity, interaction and duplicate-therapy checks, with daily dose ceilings. A contraindication blocks the prescription until a prescriber explicitly accepts it, on the record.

Consent, redaction and residency

Per-patient consent for research and model-training use, PHI redaction with a stated coverage report, and deployment in Indian data centres.

Where we actually are

Healthcare software is bought on trust, and trust does not survive discovering something later. So this is the honest state of the product.

  • BuiltReport drafting for imaging and laboratory studies
  • BuiltClinician sign-off, amendment and audit
  • BuiltCritical-result escalation with acknowledgement
  • BuiltFHIR R4, ICD-10, LOINC, RxNorm
  • BuiltMulti-tenancy, audit, consent, retention
  • Not yetClinical validation study — the first design partner's data will produce it
  • Not yetHospital SSO (SAML / OIDC) — in progress
  • Not yetSOC 2, ABDM registration, PACS integration

We are looking for two design partners

A diagnostic chain or hospital willing to run a paid eight-week pilot on real historical studies. You get the product and a retrospective validation report on your own data. We get the evidence and the clinical direction.

hello@medaiclinical.com