UDI regulation deadlines. Here’s how to make sure you’re in line.

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 […]

5 Questions You Need to Answer for Every Labeling Project

By Ken Boss At JN White™, we’ve spent years working with all kinds of labeling challenges and applications. And while every project is different, we have found that there is a consistent up-front process everyone should follow to help ensure the very best results. I like to call it the “5 Questions.” Question 1 – […]