Does a container closure integrity test (CCIT) failure always indicate a defective closure? This webinar aims to explore the various failure modes that can occur even on a perfectly sealed container. We will delve into the complexities of determining whether a CCIT failure is indicative of a true container leak or if it is caused by other factors.
The webinar will begin by examining the different scenarios that can lead to CCIT failures, including environmental conditions, equipment calibration issues, and operator errors. Understanding these factors is crucial for accurately diagnosing the root cause of a failure. Participants will learn how to differentiate between true leaks and false failures, ensuring that appropriate corrective actions are taken.
Furthermore, the webinar will highlight the importance of product-specific method qualifications. Ensuring that the test method and fixturing are suitable for your specific product is vital for obtaining reliable and accurate results. We will discuss the value of tailoring the test setup to match the unique characteristics of your product, as using a less-than-ideal test configuration can lead to false failures and misinterpretations.
By the end of this webinar, attendees will have a deeper understanding of CCIT failures, the various factors that can influence test outcomes, and the best practices for conducting accurate and reliable container closure integrity tests. This knowledge is essential for quality assurance professionals, packaging engineers, and regulatory compliance experts who are responsible for ensuring the integrity and safety of pharmaceutical and medical device packaging.
Join us to gain insights into effectively identifying and addressing CCIT failures, optimizing your test methods, and maintaining the highest standards of product safety and compliance.