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Medical Device Design and Development

Medical Device Design and Development

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.

 

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Medical Device Engineering That Provides a Solution to Your Healthcare Needs

Nectar’s medical device design and development helps to take innovative ideas and bring them to life through our development process. Starting with intensive research, Nectar uses design thinking methodology throughout every step to ensure that our products are easy to use and meet all of our customer’s needs.

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.

 

We have a robust cross-disciplinary team that can solve
almost any challenge, delivering a product that is user-centered
and optimized for manufacturing. We are one of the
best Biomedical Engineering Companies in California and
across the USA.

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Medical Device Design Engineering

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

-User-Centered Design

-Faster Market Clearance Than Competitors

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Do you have additonal Questions about our Medical Device Design & Development Services? Schedule A Consultation.

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.