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TERMINAL STERILIZATION OR ASEPTIC ASSEMBLY? CONSIDER ALL OPTIONS FOR YOUR PHARMA PRODUCT.

May 21, 2019 | (11:00AM)
USA (United States of America)
Regulation is clear that, whenever possible, products intended to be sterile should be terminally sterilized in their final container. Only if terminal sterilization is not possible, filtration or aseptic assembly should be applied. This webinar will focus on elements to evaluate prior to selecting aseptic assembly for the manufacturing of sterile drug products. Participants will learn about various mitigation possibilities for the use of terminal sterilization with gamma radiation or ethylene oxide. Understanding the fundamental differences between aseptic assembly and terminal sterilization is a critical factor in overall patient safety.
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