Labeling Scrutinized – The Importance of Inspection
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 survey conducted by PRISYM ID, 69% of respondents admitted that human error was the most frequent cause for their labeling errors, yet 57% rely on humans to spot errors. So, does inspection matter? Yes, it does! Fill out the form to download our infographic.