Skip to content
Laboratory information system

EMA Lab — the laboratory system your team deserves

Clinical LIS with 3-stage validation flow, HL7 v2 + FHIR R4 connectors, complete microbiology and antimicrobial stewardship. ISO 15189 and configurable country by country.

Schedule a demo

Key capabilities

What sets EMA Lab apart from a classic 2000s LIS.

HL7 v2 orders and results

ORM/ORU/OML with our own mapping engine — no extra middleware to connect to the existing EHR.

3-stage validation

Technical, expert with Emi assistance, professional. Full traceability, signable audit trail.

Complete microbiology

Cultures, susceptibility, MALDI-TOF and reports conditioned by organism and antibiotic.

Antimicrobial stewardship

Quarterly CLSI M39 antibiogram with multi-front alerts and a committee-ready signable report.

FHIR + HL7 v2 interop

Dual emission (Aidbox canonical + HL7 v2 to HIS) with retry sweep and visible status.

ISO 15189 quality

Indicators, internal control, non-conformities and management review — already in the dashboard.

Operational flow

Laboratory flow

From order to signed report, with audit trail and retry.

01

Order

HL7 v2 or FHIR intake — validated against catalog and patient rules.

02

Pre-analytical

Sample collection, labels, chain-of-custody control.

03

Analytical

Instrument connection, automatic read, internal quality control.

04

3-stage validation

Technical → expert with Emi → signing professional. Full audit trail.

05

Signed report

PDF + FHIR DiagnosticReport with public code-based verification.

Compliance

Configurable country by country

FHIR is the technical standard; legal compliance lives in each jurisdiction. Pick your country and see the regulations that apply and how the implementation fits.

✓
Status
Available

Reference deployment: ISP + Law 21.668 + CL Core IGs. HL7 v2 connectors and 3-stage validation flow active.

National regulations

  • Acreditación ISP / SS
    Mandatory clinical laboratory accreditation.
  • Ley 21.668 (lab clínico)
    Lab coverage inside Law 21.668.
  • DS 433/1995
    Sanitary regulation for laboratories.
  • Reglamento de Bioseguridad
    MINSAL biosafety manual.

FHIR Implementation Guides

  • CL Core 1.9.3 (Observation, DiagnosticReport)
    Observation, DiagnosticReport, Specimen — Chilean profiles.
  • Urgencia Interoperable IG
    Critical-value ER reporting rules.

Universal standards

Country-independent technical foundation that travels with the product.

HL7 v2 (ORM/ORU/OML)
Standard messaging between instruments and LIS — decades of global adoption.
HL7 FHIR R4
FHIR R4 for reports and observations — modern interoperability.
LOINC
Universal exam coding — comparable cross-country.
SNOMED CT
Clinical vocabulary for findings, organisms and results.
ASTM E1394 (instrumentos)
Connection to analytical instruments — ANSI/IEEE foundation.
ISO 15189 (calidad)
Quality management system for clinical laboratories.

Let's talk about your laboratory

30 minutes to understand your volume, your EHR and your compliance challenges — plus a live demo.

Schedule 30 minutes