VITALITI Tricorder wins Epic Innovator Prize at XPRIZE Awards
DFM is a critical aspect of the product development process. Targeting considerations of feasibility and cost-effectiveness of the product during production, DFM is a complex process. It requires careful consideration of numerous factors and a delicate balancing of often competing priorities and constraints. Unfortunately, some important elements of DFM are often overlooked, leading to problems…
Last year we wrote about how Cortex client AceAge was selected for Amazon’s inaugural Alexa Accelerator Cohort. Now, we’re proud to announce that AceAge has secured Series A funding! AceAge’s flagship product, Karie, is a medication dispenser and personal health companion with huge possibilities for care inside the home and institutional settings. Karie uses preorganized…
When AgeWell Toronto invited Cortex President Dylan Horvath to present a workshop to their network of researchers and entrepreneurs, our goal was to relate the vital importance of using ethnography to de-risk the product design process. Many startups (especially those under time pressure and budget limitations) choose to dive straight into development, assuming the product…
Outsourced Manufacturing “Welcome to the Design to Product Podcast! In this interview episode, we talked to Dylan Horvath about saving cost and time with outsourced manufacturing. Dylan Horvath is the founder and president of Cortex Design, a product design + manufacturing firm. Dylan talked about common mistakes of product builders and innovators that drive up timelines and…
Medical product development risks exist because medical device development is a complex process. It requires a thorough understanding of the risks involved. In this post, we will take a closer look at the 4 most common physical product development risks and how to mitigate them. We also tap into Cortex Design’s Founder and Chief Product…
A primer from Cortex Design. All medical devices marketed in the U.S. are regulated by the Food and Drug Administration (FDA). The FDA classifies any new medical device as either Class I, Class II, or Class III, depending on the device’s risk, invasiveness, and a number of other factors. If you want to market a…