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This solution provides organizations with complete label integrity to meet the strictest compliance requirements for FDA & EU regulations, specifically FDA 21 CFR Parts 11, 810, and 820.
Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the latest recalls trends from the industry, to see how the right software platforms can minimize the risks of labeling recalls.
Companies’ continued reliance on manual processes and disparate labeling systems often culminates in pricey product recalls.