Tiet · Studio

Turn manual handoffs into approved workflows your team owns.

A clinician in a white coat looking to the sideTiet · Studio canvas with an admission, discharge and transfer workflow
System friction

Your data is digital. The work between systems is still manual.

Handoffs by hand

Teams copy, check and reconcile the same case across systems, inboxes and spreadsheets.

Pilots that never ship

Scripts break when a screen or format changes, and generic AI pilots can't reach production systems.

No evidence trail

Every site runs the process differently, and approvals and exceptions are hard to show later.

How it works

Compose the process. Review the release. Run it with evidence.

Compose the process step by step.

Wire triggers, standards, transforms, agent, retrieval and audit steps on one canvas. Workflows act on live, normalised data from Tiet · Connect.

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Tiet · Studio canvas with a discharge-summary workflow

Embedded compliance for global healthcare standards.

HIPAABuilt againstGDPRBuilt againstISO/IEC 27001CertifiedEHDSReadiness foundationsCertified · High
Use cases

Start with one process your team can measure.

Operational answers

What teams ask before their first workflow.

Do we need developers to build a workflow?

You build workflows on a visual canvas from ready-made healthcare nodes, so most of the work is configuration, not code. Your IT team connects the source systems, and developers can call approved workflows through the API.

How long does a first workflow take?

An example plan runs six weeks: define, connect, compose, validate and go live, each with an exit criterion. Your source access, review and release readiness set the actual schedule.

How do you control the AI steps in a workflow?

Sandbox policies apply at every node, agent and tool boundary, and approval gates hold consequential steps until a person signs off. Agent configuration and AI-system risk are governed in Tiet · Agentic.

Is Tiet · Studio a medical device?

No. Tiet · Studio is workflow infrastructure with no medical purpose on its own. The intended purpose of each workflow you configure determines its regulatory route, and health institutions can build and use their own workflows under Article 5(5) of the EU MDR where its conditions are met.

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Clear the way for health.