Nectar’s 25 years of experience and extensive scientific knowledge allows us to deliver comprehensive medical device consulting services from the beginning of your project all the way to FDA approval. Our ISO 13485 certification and competent engineers create an efficient product development process for your medical device projects.
Our medical device consulting capabilities include all aspects of product development and regulatory compliance. We are experienced in turnkey development projects and can ensure that we are meeting all of your project needs, making sure your device will meet FDA compliance.
Our complete range of industry-leading product development services ensures that you have access to the resources that you need to create innovative products when you need them. We provide turnkey product development, from research to manufacturing design transfer with engagement at any stage of a project.
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.