Manufacturers looking to apply these procedures will have to provide robust validation data to reveal their equivalence to pharmacopoeial procedures. As these new systems emerge, the WHO emphasizes the value of an intensive hazard evaluation and validation system. How can sterility testing isolator manufacturers combine glove ports, transfer chambers, https://tailinscitech.wixsite.com/tailinscitech/post/applications-and-benefits-of-tailin-containment-isolator-for-handling-high-potency-materials