There’s an easier way to design, develop, and manufacture your medical devices & software. Our full-service team combines Design Thinking & Human Factors Engineering to create products that are remarkably innovative, highly effective, and follow all FDA guidance.
Bringing your medical device & software to market can be a lengthy, complicated, & frustrating process — filled with challenges like obtaining FDA approval, managing complex processes, and assembling a team of experts who are as good at their job as you are yours.
You deserve a guide who understands the journey you’re on, the path you should take, and the obstacles you’ll encounter. Of course, with decades of experience in the medical industry, Nectar does more than understand the challenges you face. We help you solve them.
Our phase-gated approach to product development is designed to bring your Digital Health device from definition to manufacturing.
We combine User Experience Design and Human Factors Engineering to create devices that are truly remarkable — and our hardware and software teams have a profound understanding of SaMD, IEC62304, and the software lifecycle.
Our entire technical team understands design controls, risk management, and usability — and our ISO 13485-certified Quality Management System facilitates the regulatory approval process by extensively documenting and tracking risks and design controls throughout the entirety of your project.
Does your medical device or software store data in the cloud? We have you covered there, too. Every cloud-based medical application we design is built from the ground up to be HIPAA-compliant.
There is an easier, and simpler, way of doing things. And it all starts with Nectar — your one-stop solution.
Our full-service team is here to help take you from napkin sketch to product rollout and beyond. Nectar combines Design Thinking with FDA principles of Human Factors Engineering & Usability, to provide solutions that are innovative, safe, and effective. The results?
In response to the Covid-19 health crisis, we partnered with BreathDirect to bring a new ventilator to market much sooner than many thought possible. By navigating the challenges posed by remote working, regulatory complexities, and extreme supply chain shortages, our ventilator received FDA approval in just ten months.
You can read about our case study here, and check out a few of our other medical devices below.
“It was an absolute pleasure working with the Nectar team. They were extremely responsive and provide clear and consistent communication throughout the project...we tasked the Nectar team with extremely challenging timelines and they rose to the occasion and kept us on track to complete the project!”
As a startup, it's not easy to find the right partners. The team at Nectar exceeded our expectations for engineering, design, and R&D — and helped Smardii with a very successful showing at the largest consumer electronics show on the planet, CES 2020.
I’ve learned through the years that the industrial design of a product in development can have an impact on the success or failure of the product launch. Nectar’s unique approach to industrial design emphasizes design concepts for manufacturability as well as human factors for ease of use, which are key factors for a successful launch.
Nectar provides advanced solutions in Development Strategy, User-Centered Design, Integrated Product Engineering, and Design Transfer to transform user needs into manufacturable products for the Medical Industry. Fill out the form below to have a Nectar Product Engineering Consultant contact you to schedule a free consultation about your project.