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Nectar’s QMS is Officially ISO 13485 Certified: What it Means and Why it Matters

For years, Nectar has been meeting and exceeding the requirements necessary to meet the ISO 13485 standards, but today we are excited to announce that we have become one of the few companies who officially hold an ISO 13485 certified Quality

Designing For Disability: How Augmented Perception and Adapting to Extremes Drives Innovation

When designing for disability, it is important to consider our preconceived ideas and our perceptions. Not only do we need to consider the ‘normalcy’ we place on having all our senses, our limbs, and an average height; we also have to consider how

Preparing to Partner with a Product Development Firm

Product development firms are in the business of helping to conceptualize, build, and develop new products that have the potential to fundamentally change markets.  Finding a solid partnership with the right development team is critical, as the

What the New FDA 510(K) Guidelines Mean for Medtech Product Development

For centuries scientists, engineers, and visionaries have been iterating and expanding on each other’s designs, even on products seemingly as simple as the light bulb Their efforts are focused on making them safer, more reliable, and more compatible

Join Nectar at the 2019 Medical Design & Manufacturing (MD&M) Expo!

This February, the largest three-day Medtech conference in North America will kick off in Anaheim, CA.  The Nectar product development team is excited to attend. We will join thousands of industry professionals and over 1,900 suppliers to discuss