Articles

Optimizing Reliability Sensitivity and Speed In Automated CCI Testing Technologies

When assuring the quality of all packaged products, testing container closure integrity (CCI) is critical, especially as related to parenteral pharmaceuticals. If there is a breach of the seal, even a microscopic one, it affects the sterility and the stability of the product – the drug may not be as effective due to oxidation or moisture ingress impacting the active ingredient.

But more importantly, a defect in the seal can lead to patient safety concerns. Parenterals are sterile preparations intended to be administered directly into the systemic circulation in humans or animals (think solutions, suspensions, and powders for injection, infusion, or implants).¹ A compromised parenteral container can act as a vehicle for microbial transmission and pose a significant risk to patient safety. Once bacteria find their way into the container, the drug is no longer a treatment but instead is a threat to the patient.

COPYRIGHT 2020, CCIT, ALL RIGHTS RESERVED PRIVACY AND COOKIES TERMS OF USE
Popup Popup