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In the highly-regulated medical device industry, labeling plays a central role. The introduction of the US FDA’s Unique Device Identification (UDI) system, the publication of the European Union’s (EU) Medical Device Regulation (MDR) in 2017, and the implementation of similar requirements in other countries have made labeling more complex – and even more critical.

As requirements continue to evolve, do you have a systematic method to labeling that will ensure compliance? Download our white paper co-authored with Loftware to find out!

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