Founded in 1986, VEI was born out of unbridled passion to meet the unmet and emerging needs faced by medical manufacturers.  At a time when manufacturing processes were advancing at an ever-increasing rate and FDA regulation continued to expand it was clear there was a need to protect against the inevitable product mix.

Since our infancy, we've grown with FDA regulations by systematically designing solutions with Title 21 CFR Part 11 compliance and validation in mind.  Throughout our history, VEI has expanded from providing solutions based purely on product mix avoidance to a comprehensive suite of quality centered solutions.  Our offerings consistently reduce cost & mitigate risk, creating a powerful package making justification common sense.  In fact, our clients repeatedly tell us that our technology has successfully prevented many CAPAs and recalls.

At VEI we're passionate about living with purpose and wholeheartedly believe that by protecting our clients and their patients we're making a meaningful difference.  In an unforgiving industry where there's no room for mistakes we've built our business on dedication to our customer and their success.  This is what we're all about, we're customer centered, market driven innovators who develop robust solutions where others only see problems.  We're going to continue to question the status-quo, develop solutions for the needs of the industry & play a critical role in advancing medical manufacturing for the better.