Developing innovative scientific devices, software, and equipment that ensure accuracy, robustness, and product equity requires an experienced partner like Nectar. Our extensive experience working on numerous product and device types—can help you navigate the design, engineering, manufacturing, and regulatory challenges associated with scientific product development.
Our Quality Management System is compliant with ISO 13485 requirements, which facilitates negotiation of the regulatory approval process. Nectar utilizes a seven-stage, phase-gate product development process that takes a new medical device from definition, specification, and design.
All the way through verification, validation, and transfer to manufacturing. We can assist you in taking scientific products from concept through commercial launch or engage with you at any phase of the process to accelerate development, minimize risk, and increase profitability.
Our portfolio encompasses a variety of first-in-class products, including those that served as a launchpad for entry into new markets.
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.