For life sciences and research

Reach governed real-world data. Keep patient data inside the hospital.

A researcher looking up
Operational bottlenecks

The data exists. Getting to it takes months.

Months per request

Every data request becomes its own legal, data and engineering project before anyone sees a record.

Data you can't compare

Sources differ in format and quality, so every cohort needs conversion and cleaning before analysis.

Privacy handled case by case

Consent, pseudonymisation and purpose rules are settled one request at a time, which slows every approval.

Platform capabilities

Build research-ready data products on one secure foundation.

Research-grade data from the source

Normalise clinical and imaging feeds, and validate wearable data from the first datapoint of a trial.

Explore Tiet · Connect
Tiet · Connect ingestion pipelines
200+Native connectors.
170+Healthcare nodes.
80+Agent templates.

Embedded compliance for global healthcare standards.

HIPAABuilt againstGDPRBuilt againstISO/IEC 27001CertifiedEHDSReadiness foundationsCertified · High
Operational answers

How Tietai fits your research programmes.

Does data leave the hospital?

It doesn't have to. Access happens inside a secure processing environment, and deployments can run fully on-premise.

Which data models do you support?

OMOP CDM 5.4, FHIR R4 and openEHR programmes, with HealthDCAT-AP metadata for discovery.

Can you support clinical trials?

Yes. Tiet · Connect enrols and validates wearable devices and monitors incoming vitals for integrity before data enters the trial dataset.

How does this relate to the EHDS?

Tiet · Govern gives you the technical foundations for EHDS secondary use: catalogue, quality, provenance, policy and controlled delivery. Legal decisions stay with your governance owners.

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Clear the way for health.