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[INFOGRAPHIC] Can Vision systems safeguard label integrity

Medical device and pharmaceutical organizations are constantly looking at ways to avoid labeling errors which are a major reason for FDA product recalls.

In a recent survey conducted by PRISYM ID, 67% of respondents admitted that human error was the most frequent cause for their labeling errors and 45% frequently experienced quality issues throughout their label production process.

So, does inspection matter? Yes, it does!

Find out the FDA regulatory compliances you will need to consider for inspection.

DOWNLOAD OUR INFOGRAPHIC TO FIND OUT MORE >

Read our blog: Survey results show how label inspection is undertaken within the industry