The purpose of the guidance is to allow food manufacturers to use the name “potassium salt” on food labels as alternative to the common name, “potassium chloride”. This salt alternative is formulated to reduce sodium content. This alternate name also makes it more clear the consumer as to what this item is. This guidance supports […]
In the midst of the COVID-19 pandemic, businesses are forced to find ways to gain efficiency. Switching to a cloud-based labeling solution enables business teams to access data, design and processes online to keep productivity high. Companies can take advantage of this change to standardize, centralize and simplify their processes. Read more about how our […]
NiceLabel’s Label Cloud Compliance can help any size business with labeling compliance needs. Check it out! Need implementation assistance? We are your go-to experts for implementation and training. Contact us at sales@pragmatyxs.com
With manufacturing plant locations and distribution facilities operating globally, companies are seeing the benefits of developing a standardized global labeling approach. Pragmatyxs has been engaged in developing solutions for global label operations for many years. We have consulted with many organizations that have multiple plant locations in migrating from their own custom legacy labeling solutions […]
When it comes to making labeling work across global supply chains, many organizations have tried to meet their evolving needs through a variety of homegrown custom solutions. Such solutions may provide steps in the right direction, but they don’t get the job done adequately. These solutions can work to solve immediate challenges but are not […]
Here are some examples of the requirements for labeling in Food & Beverage Examples: The FDA’s Food Safety and Modernization Act (FSMA), aimed at preventing food contamination across every step of the supply chain, including use of imports and exports across international boundaries. FSMA also gives the FDA authority to order a mandatory recall of […]
The European Commission legislation is introducing new compliance requirements on medical devices and creating completely new medical device regulations (MDR). Following in the footsteps of the Food and Drug administration of the US, EU has decided to adopt the Unique Device Identifier (UDI) for all medical devices and In Vitro Diagnostics (IVDR). This will be […]
UDI requirements for class 3 and class 2 devices are now behind you, but the compliance standards continue to emerge and you must maintain the ones you have already completed. Maybe your organization is impacted by all three (3) UDI class distinctions, or MDR (European UDI) standards, or you have additional requirements to maintain these […]