The importance of Design
The design of a medical device can be the most crucial phase for success when it comes to developing a medical product. A successful medical device is one that, fulfills it’s intended purpose is easy to use, but most importantly is safe and meets all regulatory compliance.
At Nectar our medical device design is executed through a six-step process that starts with extensive product and market research, to make sure that we are developing a device that meets our consumer’s needs. Our medical device development engineering team has over 25 years of experience designing innovative medical products and software that enhances people’s lives.
No matter where you are in the process with your product, from early-stage to final design tweaks our medical device design engineering takes a user-centered approach, that meets all regulatory standards to deliver a quality product that is compliant with for FDA submission.
Incorporating ISO 13485 Throughout Every Step
Here at Nectar, ISO 13485 QMS is heavily rooted into each phase of our medical device design process. From research to concept and design, all the way to testing and validation; we make sure that each input and output is carefully measured and recorded for regulatory compliance. By using quality standards and what are known as design principles to drive the design our products, this allows for complete synchronicity with our ISO 13485 QMS and thus faster times for market clearance.
Why Choose Nectar For Your Medical Device Design Needs?
-Medical Device Design experts
- ISO 13485 Quality Management System
-Faster Market Clearance Than Competitors
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.