Internet of Medical Things (IoMT) Development

NOVO is a medical product development company that helps innovative companies design and develop market-ready IoMT products.

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Years in Business
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Experts In-House
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Projects Completed

Our strategy, design, and engineering teams will help you create compliant, market-ready & connected medical devices.

Medical wearables & small devices with connectivity

Small wearables with sensors that monitor patients conditions and gives important insights to health professionals.

Large medical devices & machines with connectivity

Devices use in hospitals in various sectors (oncology, respiratory, cardiovascular, and more)

Remote Patient Monitoring (RPM) & health at home

Devices & Apps that allow health professionals to monitor patients in the comfort of their homes.

Cloud Systems with secure & accessible data from anywhere

Build the infrastructure and software architecture to securely view, process and manage data in the Cloud.

Connected Devices for asset monitoring, easy servicing & troubleshooting

Get notified if your product need servicing, troubleshoot remotely and push over-the-air updates to the firmware.

Have other IoMT ideas?

Let’s talk about your project!

ISO 13485

NOVO is ISO 13485:2016 certified for medical devices development

By co-creating with NOVO experts, your idea is in good hands. You’ll be fully confident that you’ll get a solid product and that our work will fully comply with the high expectations of the FDA and the other regulatory health organizations.

See our unique process for successful medical product development.

NOVO has helped develop a wide range of medical products including digital health systems, patient monitoring systems, oncology, cardiovascular and respiratory devices.

Identify your product's key features and market positioning

Get a cost-effective proof of concept to attract potential investors

Work with complete team of experts including strategists, designers & engineers

Have a complete and transparent vision of the project progress with our IDEAL methodology

Clear up any doubts about project documentation requirements for medical devices and software

Comply with the FDA, Health Canada and CE certification regulatory requirements

Working with NOVO allowed us to quickly show investors a certified, effective, well-designed and attractive ready-to-market medical device that addresses critical human factors in a hospital environment. We’re moving forward with additional certification and collaborating with our NOVO team on the next phase of development.

François Lellouche MD, PhD
OxyNov Cofounder

Not sure where to start?

Let our experts guide your project to success.

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