Health software. Audit-ready.

Healthcare software development where every record read is logged.

Healthcare software development covers clinical tools, patient portals, telehealth and medical AI that handle sensitive health data. In the EU that means GDPR special-category rules; US clients need HIPAA-aware design with access controls, audit logs and encryption. Yarify, a senior engineering team in Prague, builds this for hospitals, clinics and health companies, including medical AI with human review and HL7/FHIR integration with hospital systems.

Built in from day one

  • Audit logs

    Who saw which record, and when

  • Least-privilege access

    Roles mapped to real clinical work

  • Human-in-the-loop AI

    Clinicians sign off every output

  • HL7 and FHIR

    Connectors to EHR, LIS, scheduling

  • GDPR by design

    Minimised data, EU hosting

Healthcare software development we ship

  • Medical AI software

    Decision support, document summaries, triage assistants and classification, with evaluation sets, monitoring and clinician review.

  • Hospital integrations

    HL7 v2 and FHIR connectors with mapping, validation and retry queues, tested against real message samples.

  • Patient portals

    Booking, secure messaging, document upload, consent management and multilingual screens.

  • Clinical workflow tools

    Referrals, intake and reporting off paper. See replacing manual data entry with AI.

  • Telehealth and monitoring

    Video consultations, device data ingestion and alerting dashboards for care teams.

  • Health product MVPs

    A fixed-price first version with the security posture to pass a hospital procurement review.

Stethoscope on a desk next to medical paperwork

Compliance without the theatre

We are engineers, not auditors. We hold no HIPAA certification, and no software is HIPAA compliant on its own. We make your compliance work straightforward.

  • GDPR for health data

    Minimisation, purpose limitation, consent records, subject access and deletion, and EU hosting where required.

  • HIPAA-aware for US clients

    Encryption, unique user IDs, session timeouts, audit logs and hosting where your provider signs a business associate agreement.

  • Queryable audit logs

    Append-only records of who viewed or changed what, exportable for your DPO or a hospital's security review.

  • Medical device scope flagged

    If EU MDR or FDA rules may apply, we say so on the scoping call, before the architecture is fixed.

Engineer monitoring secure servers in a data room

Medical AI in production

AI software for a hospital: human review of every output, audit logging, integration with existing systems. Anonymised at the client's request.

From data map to pilot

  1. Data map · Week 1

    Every piece of health data: source, storage, access, retention. The backbone of your DPIA.

  2. Architecture and access · Weeks 1–2

    Roles, audit logging, encryption, hosting region and an AI evaluation plan agreed in writing.

  3. Build on synthetic data · Build

    No real patient data in development. Weekly demos for clinical stakeholders, pull requests in your repo.

  4. Validate and pilot

    Integrations tested on real message samples, AI measured against the agreed set, then a controlled pilot with monitoring.

What drives the cost

Regulated builds cost more, honestly. Vendor surveys put compliance overhead at roughly $20k–$80k on top of an MVP, and regulated AI projects at 20–40% more. See the AI development cost guide.

The drivers: number of hospital integrations, whether AI affects clinical decisions, data residency, audit depth and user roles. Our price is a fixed written quote after a free scoping call.

Inherited a health app nobody trusts?

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Related services

Questions buyers ask us

Is your healthcare software HIPAA compliant?

No vendor can honestly sell software as HIPAA compliant on its own, and we hold no HIPAA certification. Compliance depends on how you operate the system. We provide HIPAA-aware design: encryption, access controls, audit logs and hosting on providers that sign business associate agreements.

How do you handle GDPR for patient data?

We start with a data map: what is collected, why, where and for how long. Then minimisation, access logging, subject access and deletion, and EU hosting where required. Yarify is a Czech company, so we work under EU law and sign a data processing agreement.

Can you integrate with our hospital EHR?

Usually, yes. Most hospital systems expose HL7 v2 interfaces, FHIR APIs or both. We build connectors with mapping, validation and retry queues and test them against real sample messages. The hospital IT access process often sets the timeline more than the code does.

How do you make medical AI safe to use?

Outputs are drafts until a qualified person accepts, edits or rejects them, and each decision is logged with model version and input. We agree an evaluation set with clinicians before choosing a model and monitor accuracy after launch.

Is our software a medical device?

It might be. Software that informs diagnosis or treatment can fall under EU MDR or FDA rules. That is a regulatory question, so we flag it on the scoping call and recommend specialist advice early, then build to the change-control process your path needs.

How much does healthcare software development cost?

Market data puts a regulated MVP at the normal MVP range plus roughly $20k–$80k for compliance work, with AI adding more. We give a fixed written quote after a free scoping call, and on fixed-scope work our estimation overruns are our cost.

Health data, handled like it matters.

Book a free 30-minute call with the engineer who would build it. Leave with scope, risks and a fixed quote.

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