Automation Of Class III Medical Device Packaging

VeriPac LPX-2

When assuring the quality of all packaged products, testing container closure integrity (CCI) is critical, especially as it relates to Class III medical devices. If there is a breach of the seal, it affects the sterility of the device and may present a significant quality concern at a critical moment of use.

Traditional container closure integrity (CCI) testing methods can be destructive, time-consuming, and limited in their effectiveness and reliability, as they are probabilistic methods. Explore the need for sensitive, fast, and reliable automated CCI testing technologies and how existing solutions can help achieve optimum quality goals for medical device manufacturers.


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