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‘Labeling Challenges’ Blog Series, Issue #5 Label Defect Control - Achieving zero-defect labeling

With the introduction of UDI, the need for medical device manufacturers to examine systems, processes and operations is intensifying. Product recalls in the medical device industry are increasing – impacting operational efficiencies and profitability. Labeling errors are a common cause of recall, but they can be easily avoided. The introduction of automated vision systems means there are more effective, efficient and secure ways of ensuring zero-defect labeling.

By integrating automated vision inspection with label lifecycle management software, medical device manufacturers can manage and document labels through design, approval, print and inspection. This end-to-end approach gives greater visibility and control of the entire process, and supports FDA compliance.

To find out more, watch our best practice guide to achieving zero-defect labelling which can be viewed here.
This webinar presents best practices to help:

• Understand why print verification systems are becoming an essential part of the production line
• Discover why your medical device label production may not be meeting FDA compliance requirements
• Achieve insight into best practices for managing defect control

Watch the Vision Systems Webinar Here