SCHOTT iQ® Integribag

SCHOTT iQ® Integribag
Product Description

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® 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® Integribag, any additional decontamination steps, such as E-beam or manual alcoholic disinfection wipes, are no longer needed.

SCHOTT Pharma AG & Co. KGaA

  • DE
  • 2015
    On CPHI since

SCHOTT Pharma AG & Co. KGaA

  • DE
  • 2015
    On CPHI since

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SCHOTT Pharma AG & Co. KGaA resources (2)

  • News Pharma supply chain companies form alliance to accelerate sustainability

    Alliance to Zero aims to facilitate the transition of the pharma sector to reach net zero emissions target
  • Webinar End to End Sterility Assurance for Next Level Risk Mitigation

    In this webinar, originally broadcast as part of the Pharmapack Europe show, Dr. Robert Lindner, Global Product Manager RTU Vials, SCHOTT AG will discuss how sterile integrity is indispensable in aseptic fill-and-finish operations. Pharmaceutical companies pay highest attention to producing high quality drugs and safekeeping their efficacy during fill-and-Finish and beyond. The risks of contaminated batches leads to recalls, high costs, reputation loss and in the worst scenario may harm patients’ wellbeing. Hence, it is the pharma company’s obligation to ensure the sterility of all components when entering the aseptic filling core - which is possible, yet cumbersome with the RTU solutions that are currently available within the industry.