Developing innovative medical devices & equipment that ensure patient safety and product equity requires an experienced Medical Product Development Company like Nectar. We have extensive experience in Medical Device Development working on numerous and varied device types—including consumable, point-of-care, diagnostic, surgical devices, and more. With this experience, Nectar can help you navigate the design, engineering, manufacturing, and regulatory challenges associated with medical product development, all while keeping a user-centered design focus.
Our ISO 13485 Certified Quality Management System facilitates the regulatory approval process by extensively documenting and tracking risks and design controls throughout the project. Nectar utilizes a phase-gated product development process that takes a new medical device from definition, specification, and design all the way through verification, validation, and transfer to manufacturing.
All the way through verification, validation, and transfer to manufacturing. We can assist you in taking medical devices from concept through commercial launch or engage with you at any phase of the process to accelerate development, minimize risk, and increase profitability.
We have a robust cross-disciplinary team that can solve almost any challenge, delivering a product that is user-centered and optimized for manufacturing.
Our portfolio encompasses a variety of first-in-class products, including those that served as a launchpad for entry into new markets as well as next-gen, industry-leading products.