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! Complete the form to download our infographic.
You can also read our whitepaper: A Clear Vision: Developing the right strategy to assure compliant labeling inspection