Innovation Without Borders: 
🇺🇸 Why U.S. Teams Still Look to Canada for Product Development 🇨🇦

All-in-One Medical Software Design & Development Firm

We design and develop digital experiences that have an impact with your users.

We Help You Create Compliant, Market-Ready Medical Software

Writing code is just one of many things our software engineers excel in. They work closely with our strategists, UX/UI designers, embedded software engineers and quality assurance teams to choose the perfect technology stack.

We develop iOS and Android mobile applications, web portals, desktop applications, user interfaces, and much more. Working closely with our firmware team, we build Cloud (Amazon web service and Google Cloud) and IoT solutions. We also collaborate with the user interface (UI) and user experience (UX) design teams to create intuitive experiences for your users.

Digital Health & Remote Patient Monitoring

Medical Software Development (SaMD & SiMD)

Electronic Health Records (EHR) Software

Telemedicine Platforms

Patient Portal Software

Healthcare & Medical Practice Management Software

Mobile Health Apps

Custom Health Data Analytics Platforms

Need Something Else?

Our full-stack software engineers develops powerful, interactive, and connected applications

Innovation Strategy

Human Factors Engineering

UX & UI Design

Software Architecture

Technology & Stack Selection

User Interface Integration

System Integration

Front-end Development

Back-end Development

Web, Desktop & Mobile Apps

Risk Management

DevOps & App Deployment

Maintenance & Support

Project Management

Our Quality Management Process Follows the Highest Development Standards

ISO 13485:2016

ISO 14971:2019

IEC 62304:2006/AMD1:2015

IEC 60601-1 Ed. 3.2

IEC 62366-1:2015/AMD1:2020
At CLEIO, our integrated design process follows the highest development standards. From concept to market, all our teams are involved and collaborate to make the product evolve according to the recommendations of our quality assurance experts.

Our ISO-13485 certification means that our development activities are controlled and structured by audited and certified processes. These ensure our service quality and the satisfaction of our customers.

In addition, our teams develop your products according to applicable harmonized standards to meet the medical device’s regulatory requirements. It speeds up the time to market and facilitates product approval by relevant authorities.
PROJECTS

Discover the Innovations
We’ve Brought to Life

From life-saving MedTech innovations to intuitive digital experiences, breakthrough consumer products, and cutting-edge industrial solutions, explore our projects.

Launch Your Medical Device with Confidence – Our Experts Are Here to Help

Facing roadblocks? Need external support? Our experts will answer your questions, help you navigate challenges, and guide you through every stage of your product development journey.

We are ISO 13485 certified. It means that our development process for medical devices is fully compliant with the high expectations of the FDA and other healthcare organizations. For you, it’s the assurance that your idea is in good hands.

Get a Free, 45-minute Consultation with our Industry-Leading Experts

TESTIMONIALS

What our partners
say about us

300+ Customers

Let's talk about your project