SCHOTT iQ(R) Integribag

Sterile integrity is indispensable in aseptic fill-and-finish operations. Pharmaceutical companies pay highest attention to mitigating the risks of contaminated batches, which lead to recalls, high costs and reputation loss. Ensuring the sterility of all components when entering the aseptic filling core is possible, yet cumbersome with the RTU solutions that are currently available within the industry. SCHOTT iQ(R) Integribag's quality-by-design approach design takes sterility one step further by not only the inside of the RTU tub, but also the outside of the tub and the protective tub layer. This is possible thanks to the bags material, which has a high puncture resistance. It leads to a lower probability of failures and complaints. Additionally, the bags seal is tamper-evident and can easily be inspected by pharma companies as well as CDMOs. With the SCHOTT iQ(R) Integribag, any additional decontamination steps, such as E-beam or manual alcoholic disinfection wipes, are no longer needed.