Blog

Discover what makes us tick by reading about what makes us talk.

Our son Charlie

Stephen Bates, Founder and CEO

“With life’s many twists and turns, my wife and I were unfortunately introduced to the world of medical equipment as parents at an early age.  Our second son, Charlie, was born with severe epilepsy and autism.  As if the autism was not enough of a diagnosis, it was really the epilepsy that was debilitating.  Little did I know

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Does The Acronym UDI Give You Heartburn?

Global Interconnect

Does the acronym UDI give you heartburn? How prepared and confident are you when it comes to meeting FDA’s Unique Device Identification mandate?   As part of Global Interconnect’s continual pursuit to expand our capabilities and satisfy the rising demands of the marketplace and our customers, we are excited to announce that GII now has

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Easing into the Regulatory Process

Global Interconnect

The regulatory process can be an intimidating cycle for start-ups and seasoned companies alike. In order to better understand the rules and regulations and be an asset to our customers, Global Interconnect, Inc. (GII) hired Dr. Steven Brooks M.D. M.B.A.F.A.C.C. as the company’s first Chief Medical Officer in May of 2017. Dr. Brooks has consulted various medical

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How Is Your Experience With Your Manufacturer?

Global Interconnect

Today’s supply chain process has become more automated, which has its pros and cons, but the ladder leads to uncertainty. It has created a system with unanswered phone calls, emails with late replies, and frustrating delays. Nobody wants to feel like just another account when working with a custom manufacturer. They want timelines hit and an

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Global Interconnect Adds Chief Medical Officer To Offer Product Development Insight

Global Interconnect

To further educate ourselves and remain knowledgeable about successful product development and launches within the medical device sector, Global Interconnect hired Dr. Steven Brooks M.D. M.B.A.F.A.C.C. as the company’s Chief Medical Officer in May of this year. With an impressive background of engagement in various stages of the medical device lifecycle, the wealth of regulatory

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