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  3. Medical device software development services
SOLUTIONS

Medical device
software development services

Code for care. Software for life.

Build your remote patient monitoring solution with domain experts. Backed by 15+ years of experience.

Our medical device software
development services

We develop intelligent embedded software that powers the core functionality of medical devices.

  • Implantable devices: Pacemakers, insulin pumps, cochlear implants
  • Diagnostic equipment: Ultrasound machines, ECG monitors, X-ray systems
  • Therapeutic devices: Infusion pumps, ventilators, surgical robots

Our SaMD solutions empower healthcare providers and patients with innovative tools for diagnosis, treatment, and monitoring.

  • Telemedicine platforms: Remote patient monitoring, virtual consultations
  • Medical image analysis: AI-powered image interpretation
  • Patient management systems: Electronic health records, appointment scheduling

Our software for IoT solutions enhance patient care, improve operational efficiency, and drive data-driven decision-making.

  • Wearable health devices: Fitness trackers, smartwatches with health monitoring
  • Remote patient monitoring systems: Continuous glucose monitoring, blood pressure monitoring
  • Smart hospital environments: Asset tracking, patient location systems

Medical device software features

What we develop as a medical device software development company.

For patients and end users

  • Reliable data capture from medical devices and sensors
  • Clear feedback on measurements, device status, and usage
  • Simple, guided interfaces designed for non-technical users
  • Secure transmission of health data to care teams or platforms
  • Interfaces adapted to specific devices, therapies, and patient populations

For clinicians and operators

  • Accurate, real-time visibility into device-generated data
  • Clear trends and alerts based on clinical thresholds
  • Access to historical measurements and usage logs
  • Tools to support clinical decision-making, not overwhelm it
  • Workflows aligned with real clinical and operational processes

For the platform and device ecosystem

  • Secure data ingestion from hardware and connected devices
  • Stable firmware-to-software integration
  • Role-based access and permission control
  • Full traceability of data, actions, and system changes
  • Custom platform features aligned with IEC 62304, FDA, MDR, and other regulatory requirements

Let’s work together!

Discuss your medical device software with our engineering team

Case studies

QAUSA
Abbott - Flyant client

Quality Engineering at Scale for a Global Glucose Monitoring Platform

Our collaboration with Abbott Laboratories to build and maintain a highly stable QA ecosystem for a cloud-based glucose monitoring platform used by millions of doctors and patients.

Legacy modernizationEngineeringQAUK
GoodShape - Flyant client

Modernization & Quality Engineering for an Employee Wellness Platform

A long-term technology partnership supporting a UK workforce well-being leader in modernizing its platform, rebuilding architecture, and embedding QA directly into delivery.

EngineeringUSA
GazeHealth - Flyant client

Mental Healthcare Analytics Platform Development

A long-term engineering partnership supporting a US-based healthcare technology company in building a modern EMR and analytics platform for data-driven mental healthcare.

Why choose us?

Trusted to deliver when failure is not an option.

Healthcare focus

Deep experience delivering regulated healthcare software.

Delivery discipline

Predictable execution backed by mature delivery and governance.

Trusted by investors

Chosen by PE and VC-backed companies globally.

Senior engineering teams

High-calibre engineers with healthcare context.

Commercial assurance

Clear contracts, legal safeguards, financial accountability.

Proven execution

30+ healthcare products delivered and supported.

Compliance is part of the delivery

Regulatory alignment is built into engineering, quality assurance, and release processes across healthcare systems.

Our technology stack

CSS

Angular

HTML

JavaScript

Next.js

React

Vue.js

TypeScript

.NET

ASP.NET

Vaadin

Node.js

Nest.js

Koa.js

Express.js

Python

Django

Java

Spring Boot

Hibernate

Play Framework

Ruby

Ruby on Rails

Go

Fiber

.Net Core

ASP.Net Core

Entity Framework Core

Kotlin

Android SDK

Android Studio

Android Jetpack

Objective-C

Swift

iOS SDK

Xcode

Cocoa Touch

React Native

Expo

Flutter

Ionic

Docker

Kubernetes

Jenkins

Puppet

Azure DevOps

GitLab CI

Grafana

Prometheus

Azure SQL database

Google Cloud SQL

Google Cloud Datastore

Microsoft Azure

Amazon Web Services

Google Cloud

Cucumber

Selenium

Appium

Mocha

Playwright

Robot Framework

Specflow

TestNG

WebdriverIO

Selenide

Calabash

Watir

Codeception

Cypress

HCL AppScan

Nessus

NMAP

BurpSuite

Acunetix

OWASP ZAP

Metasploit

Wireshark

DBeaver

Rdp-Sec-Check

SNMPCHECK

AiR

SSLSCAN

JMeter

Load Runner

Visual Studio

Rest API

GraphQL

Apiary

Bluetooth Low Energy API

Apple Pay

Google Pay

Apple Maps

Fingerprint API

Postman

Swagger

Charles Proxy

Ready API

ACCELQ

Katalon Platform

REST-Assured

SQL Server

MySQL

Oracle

PostgreSQL

Cassandra

MongoDB

Firebase

SQLite

RethinkDB

Amazon S3

Redshift

DynamoDb

Amazon RDS

DocumentDb

Amplify

Lambda

Amazon EC2

Elasticache

Azure Datalake

Blob Storage

CosmosDb

SQL Database

Synapse Analytics

Figma

Sketch

Adobe Xd

Invision

Marvel

Photoshop

Illustrator

FigJam

Mirro

FlowMapp

ProtoPie

Proto.io

Spline

GoogleWebDesigner

Adobe After Effect

Mural

Notion

Human Interface Guidelines

Material Design

Our approach to medical device
software development

A structured process for delivering medical device software that remains safe, compliant, and reliable in real-world use.

Strategy

Design

Develop

Our approach process colorful

Get in touch

You have a vision. We have the expertise and resources to get you there.

Frequently asked questions

We start medical device software development by reviewing clinical intent, risk class, and regulatory exposure before talking about features. Requirements are mapped to intended use, hazards, and verification needs early. This avoids redesign later when compliance gaps surface. Scope is adjusted as evidence, not assumptions, emerges.
Our medical device software development services cover architecture decisions, documentation, validation planning, and release controls. We align development tasks with verification and traceability from day one. This keeps engineering and compliance moving together instead of blocking each other. Code is only one part of delivery.
As a medical device software development company, we work as an extension of your internal team with clear ownership boundaries. Product decisions stay with you; engineering and quality execution stay with us. Communication is structured around milestones, risks, and evidence readiness. No black boxes, no hand-offs at the end.
Medical device app development timelines depend on risk class, integrations, and required validation depth. We plan in phases with defined checkpoints instead of fixed long-term promises. Early builds focus on proving safety-critical paths and data flows. This gives realistic forecasts as the product matures.
Many medical device software development companies treat compliance as documentation after development. We design systems so compliance artifacts are produced as a by-product of engineering work. This reduces rework and audit stress. It also keeps teams focused on real risks, not paperwork volume.
Medical device software engineering starts with separation of safety-critical and non-critical components. We design for controlled change, clear interfaces, and predictable failure modes. Scalability is addressed without compromising validation boundaries. Architecture decisions are documented with regulatory context in mind.
In medical device software development, integrations are treated as risk surfaces, not simple connectors. We validate data integrity, timing, and error handling across devices, cloud services, and clinical systems. External dependencies are isolated to limit blast radius. This approach simplifies future updates.
Our medical device software development services align daily engineering work with applicable standards and regulatory expectations. We maintain traceability between requirements, risks, tests, and releases as the system evolves. Compliance is reviewed continuously, not just before submission. This avoids late surprises.
As a medical device software development company, we design security controls into architecture, not as add-ons. Access control, encryption, and auditability are implemented based on data sensitivity and clinical impact. Security decisions are documented for regulatory review. This keeps patient data protected and defensible.
Medical device app development can run as a dedicated team, a phased delivery model, or targeted augmentation. The choice depends on internal maturity and regulatory workload. We adapt the model as risk profile and scope change. Engagement structure stays flexible, accountability does not.
Systems from medical device software development companies often fail when scaling breaks validation assumptions. We plan scalability with controlled configuration changes and repeatable verification steps. Performance growth does not bypass safety controls. Scaling remains predictable and auditable.
Medical device software engineering does not end at release. We support change impact analysis, regression strategy, and controlled updates over the product lifecycle. Each change is evaluated for clinical and regulatory impact. This keeps products stable years after launch.

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