Consumers today are more educated on the products they purchase and are very conscious of what is deemed “healthy.” We have recently seen waves of food manufacturers facing lawsuits over false advertising, especially focused around foods labeled “healthy” and “natural.” Ryan Fournier, an international trade associate for law firm Armstrong Teasdale lists items manufacturers must […]
A great blog post from Oracle (www.Oracle.com) with our CEO Paul Van Hout discussing how vital it was for our business to migrate to the cloud to ensure all ends of our business are reliable and efficient. Read more in the link below: https://blogs.oracle.com/midsize/small-business-big-technology
Paul Van Hout, Pragmatyxs CEO at Oracle Open World discussing the benefits of Oracle Cloud and how those benefits are utilized by Pragmatyxs. https://youtu.be/G8vt-jcbFVc
Pragmatyxs SmartLabel (PXSL) wasn’t created for just improving print operators user experience on the manufacturing and labeling line. It was also created as a tool that can offer proper validation, record history and security. Pragmatyxs is constantly evolving PXSL to not only meet customer requirements but also to improve processes that organizations haven’t even thought […]
Managing label and barcode print operations can be a heavy task for any administrator, especially when it comes to controlling operations across the globe. Ensuring that the correct label and the quantities printed are important for supply chain movement and accuracy. A disciplined approach to global label printing that is extended to all of the […]
The FDA has recently published the final rule implementing section 708 of the Food and Drug Administration Safety and Innovation Act (FDASIA). The rule provides the FDA with an administrative process for the destruction of certain drugs refused admission to the United States. Many of these drugs come into the United States via international mail. […]
The Pharma and Medical device industry is well informed on the changes being implemented for better device identification and issue tracking known as the UDI ruling. The first wave of requirements for Class III devices is now behind us and Med Device Online sat down with Jay Crowley, VP and UDI Practice Lead at USDM […]
Counterfeit drugs have become a growing issue in the Medical Manufacturing industry and as technology advances we are seeing more and more occurrences. We have addressed in previous posts the major risks in counterfeit products and how they can have a severe impact on the consumer. We rely on the integrity of the drug supply […]
The future of RFID tagging is looking more promising than ever. The RFID Journal expects the industry to reach over $5.4 Billion by 2020. A unique story we discovered on RFID Journal’s site was one that came from the operating rooms at the University of Tennessee Medical Center; they had implemented the tracking of consumable […]