Yameo engineers healthcare software for clinical environments — patient management systems, EHR/EMR integrations, telemedicine platforms, and medical device software. Built to HIPAA, GDPR, and MDR standards. Fixed price. Zero data breaches in 21 years.
Six core solution categories for healthcare organisations. Every one is delivered with clinical workflow expertise and compliance built in at the architecture level.
End-to-end patient record management with appointment scheduling, care pathway tracking, and clinical documentation workflows. Role-based access controls, HIPAA-compliant audit trails, and GDPR consent management included as standard.
Evidence-based alerting, drug interaction checking, and diagnostic support tools that integrate into existing clinical workflows without disrupting them. Designed with clinicians to reduce alert fatigue while maintaining safety-critical coverage.
HL7 FHIR R4-compliant integrations connecting your applications to Epic, Cerner, MEDITECH, and national health information exchanges. We handle the complexity of clinical data mapping so your team focuses on care delivery, not middleware.
Secure video consultation, asynchronous messaging, and remote monitoring platforms for primary and specialist care. Built with end-to-end encryption, GDPR-compliant data residency controls, and accessibility to WCAG 2.1 AA standards.
Software as a Medical Device (SaMD) and device-companion applications developed under IEC 62304 processes with full traceability from requirements to test evidence. We support CE marking under EU MDR and FDA 510(k) submission documentation.
Population health dashboards, outcomes reporting, and operational analytics platforms that surface actionable insights from clinical data. Built with de-identification, data governance controls, and NHS/EU data sovereignty requirements in mind.
Healthcare software that fails a compliance audit puts patients at risk and organisations in breach. Every framework below is a built-in constraint — not an optional add-on.
Four phases built for clinical environments. Every deliverable is traceable to a requirement. Every decision is documented. Every release is tested against the regulatory framework that governs your system.
Clinical workflow mapping, data flow analysis, regulatory classification, and stakeholder interviews with clinical, IT, and compliance teams. Output: fixed scope, regulatory risk register, and a price locked before build begins.
System architecture, data sovereignty model, HL7 FHIR integration design, and clinical UX prototypes reviewed with clinicians before development begins. For SaMD projects, IEC 62304 software architecture documentation is produced here.
Sprint-based development with fortnightly clinical stakeholder demos. Every feature is verified against its compliance requirement at the PR level — not deferred to a compliance phase. HIPAA and GDPR controls are unit-tested.
Clinical user acceptance testing, penetration test, OWASP scan, accessibility audit, and regulatory review before go-live. For SaMD: full technical file compilation support. Post-launch SLA with the same engineering team.
21 years building for organisations where software failures have clinical consequences. These are the four things healthcare clients tell us matter most.
We've built software used daily by doctors, nurses, and patients for over two decades. Our engineers understand clinical workflows, not just technical patterns. We design for the nurse in a hurry, not just the architect reviewing diagrams.
Patient data never leaves the jurisdiction you specify. We architect for data residency from day one — cloud regions, encryption at rest, key management, and access logging are configured before a single byte of PHI touches the system.
HL7 FHIR R4 APIs built into every new system. We don't create data silos — we build systems that share data with your existing EHR, national registries, and health information exchanges using standards your IT team can maintain after we're done.
For medical device software, we produce the IEC 62304 technical documentation, risk management files, and clinical evaluation support needed for CE marking and FDA 510(k) submissions. We've supported regulatory submissions in 5 EU countries.
Share your clinical requirements and we'll respond within 48 hours with a detailed scope, regulatory compliance checklist, and fixed price — no obligation.
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