Just one week after BLUE is scheduled to exhibit at PACK EXPO in our hometown of Chicago, we’ll be hitting the road and heading West. Our destination will be the Pharma and Device Packaging and Labeling Conference taking place in San Mateo, Ca, November 16-17. This trip promises to be a big event ... Read More
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Matt Gordon on June 20, 2016
Your company’s digital assets are a crucial part of your business. Each one costs time and money to make, and is a hard-working part of your brand identity. And digital assets can have a long lifespan. They can be used and reused any number of times on packages, labels, advertising, point of ...
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Admin on March 23, 2016
Pharma companies who fail at the labeling process are at serious risk of failing as a company. Lost revenue from missed shipping deadlines are a tame example of the potential consequences of a flawed process. That’s because mislabeled pharma products are dangerous! They can lead to ...
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Admin on December 8, 2015
The running back bursts through a hole in the defensive line, ball tucked tightly under his arm, the hash marks beginning to blur as he gains momentum. He sheds one tackle, then two, as his eyes gaze wildly at the end zone he sees that the path is obscured by defenders, but he remains determined to ...
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Admin on September 15, 2015
For Pharma leaders, taking on the challenge to move your organization toward Labeling & Artwork Excellence can be daunting when you look at it from the very beginning. Don’t let a blank page overwhelm you. Instead, get a head start. One easy way to generate early momentum is to build on the ...
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Admin on August 4, 2015
For many brands, the package has taken on a new role, beyond just being a delivery device for the product or an alluring brand image on shelf. With renewed recent attention from regulatory entities in the United States and European Union, the package is increasingly being viewed and regulated as a ...
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Admin on June 24, 2015
In the Pharmaceutical industry, the meticulous work required to complete the software validation process is not something many professionals wish to repeat more often than necessary. Certainly, the initial implementation of a validated system should not have to be endured more than once. Though the ...
