Internet of Medical Things (IoMT) Development
NOVO is a medical product development company that helps innovative companies design and develop market-ready IoMT products.
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.
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.
- Improve collaboration.
- Accelerate Impact.
- Reduce complexity.
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.
OxyNov Cofounder
Not sure where to start?
Let our experts guide your project to success.
