$ cd industries/healthcare

Healthcare Software
HIPAA from Day One.

Patient data handling, clinical workflow software, and EHR integrations built to HIPAA, HL7, and FHIR standards from the first sprint, not retrofitted after the fact.

FHIR R4 compliant APIs
ISO 13485 QMS ready
100% PHI encrypted
Growing practice
// Capabilities

What We Build

Every system we deliver for healthcare clients is designed for regulated production, not prototyped and handed over.

EHR / EMR Integrations

Bidirectional FHIR R4 integrations with Epic, Cerner, and proprietary hospital systems, with full HL7 v2 compatibility layers.

Clinical Workflow Software

Scheduling, patient communication, care coordination, and clinical decision support tools that fit into existing clinician workflows.

Medical Device Software

SaMD development under EU MDR and ISO 13485 QMS, with full traceability and IEC 62304 lifecycle management.

Patient Data Platforms

PHI-compliant data lakes, analytics pipelines, and reporting platforms for population health management and clinical research.

Telemedicine Platforms

Video consultation scheduling, asynchronous messaging, e-prescription workflows, and patient journey management: HIPAA and GDPR compliant by design.

Consent & Data Rights

Patient consent lifecycle management, data subject access request automation, and right-to-erasure workflows, built for GDPR and HIPAA simultaneously.

// Compliance

Where Patient Safety Meets Software.

Healthcare software carries the highest compliance burden of any sector we work in. Every standard below is built into our architecture, not bolted on after audit findings.

HIPAA
Health Insurance Portability and Accountability Act. PHI handled with strict access controls, audit logging, encryption at rest and in transit, and breach notification protocols.
✓ PHI controls implemented
HL7 FHIR R4
Health Level 7 Fast Healthcare Interoperability Resources. Bidirectional FHIR R4 APIs for seamless data exchange between EHR systems, devices, and applications.
✓ R4 compliant APIs
EU MDR
EU Medical Device Regulation. SaMD classification, clinical evaluation, and post-market surveillance built into the development lifecycle from day one.
✓ MDR lifecycle management
ISO 13485
Quality Management System for medical devices. Full traceability, IEC 62304 software lifecycle, and design history file management throughout the development process.
✓ QMS-ready delivery process
GDPR
Patient data handled under GDPR with data minimisation, explicit consent management, and data subject rights enforcement. Cross-border data transfer controls implemented.
✓ Consent-first design
DSPT
Data Security and Protection Toolkit (NHS England). Mandatory information governance standard for NHS systems and their suppliers, built into our delivery model.
✓ NHS-ready architecture
// Our Approach

A Growing Practice. Serious Standards.

Healthcare is a growing area for Yameo. We bring the same compliance rigour we've applied to insurance (Solvency II, DORA) and banking (PCI DSS, MiFID II) to clinical systems, from the first line of code.

Compliance-First Architecture

HIPAA, FHIR, and EU MDR aren't retrofit: they're sprint zero decisions. We document architecture decisions against compliance requirements from day one.

Clinical Workflow First

Software that doesn't fit clinician workflows doesn't get used. We embed clinical process discovery in our requirements phase, before a line of code is written.

Transparent About Our Experience

Healthcare is new territory for us. We're honest about that. What we bring is proven compliance engineering from adjacent regulated domains and a genuine interest in doing it right.

// By the numbers

Healthcare Standards We Build To

FHIR R4
Compliant APIs
ISO 13485
QMS Ready
100%
PHI Encrypted
HIPAA
Compliant Architecture
EU MDR
SaMD Lifecycle
GDPR
Consent-First
// What We Do

Related Services

Custom Software Development AI Projects Strategic Development Partners System Transformation All Services →
// Next Step

Have a Healthcare Project?

If HIPAA, FHIR, or EU MDR compliance is the hard part of your project, we're interested in talking. We bring regulated-industry rigour. And we're honest about where we're building experience.

Get in Touch →