Fhirex by Examya
FHIR/Core-CL pilot service for clinics, laboratories and HIS/EHR systems: synthetic data, interoperable clinical resources and technical evidence before touching production.
Fhirex by Examya is a service for starting clinical interoperability pilots using FHIR R4 and Core-CL alignment, without connecting production systems or exposing real patient data on day one.
The proposal is simple: take a focused clinical workflow, represent it with FHIR resources, use synthetic data and generate technical evidence so medical leadership, IT teams and HIS/EHR vendors can evaluate the path before a production integration.
FHIR pilot service
- Pilots with synthetic data: initial validation without PII or unnecessary risk over real clinical data.
- Clinical resource mapping:
Patient,ServiceRequest,Observation,DiagnosticReport,AuditEventandProvenancedepending on the use case. - Core-CL alignment: a technical approach to the Chilean standard for discussing concrete contracts with IT teams and vendors.
- Evidence for IT review: payloads, traceability, expected errors, integration boundaries and criteria for moving toward production.
Who it is for
Fhirex is designed for clinics, laboratories, healthcare providers, HIS/EHR vendors and teams that need to test interoperability without putting critical systems at risk from the start.
A pilot can begin with something as concrete as representing a medical request as a ServiceRequest, linking it to a synthetic patient, returning results as Observation/DiagnosticReport and leaving auditable evidence.
What it does not promise
It is not a formal Core-CL certification or a universal integration ready in one week. It is a safer, honest way to start small: one use case, synthetic data, clear FHIR contracts and technical review before production.
Services and features
- Use-case design: definition of the initial clinical workflow, actors, involved systems and expected evidence.
- FHIR R4 modeling: representation of requests, synthetic patients, results, diagnostic reports and auditable events.
- Core-CL technical validation: review of contracts, payloads, codes, traceability and compatibility with HIS/EHR or LIS systems.
- Safe pilot environment: testing with synthetic data to reduce regulatory risk before discussing production.
- Findings report: documentation of gaps, technical decisions, risks and next steps for the IT team.
Expected outcome
At the end of the pilot, the team has concrete evidence to decide whether the clinical workflow is interoperable, what adjustments it needs and what conditions must be met before moving toward a production integration.