Starting in 2013, the US Food & Drug Administration (FDA), the European Commission (CE), and other regulating bodies established new labeling requirements for medical devices. The goals were to increase patient safety, increase supply chain efficiencies, and improve the traceability of medication and medical devices. These regulations were phased in over time, with the first […]
Read MoreFrom prime labels to membrane switches, the materials we use on a day-to-day basis can have a huge impact on the products we deliver to our customers. That’s why I like to keep a close eye on new developments, inside and outside of our business. As many of us know, one of the great advantages […]
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