Cleaning, Sterilization & Bio Decontamination White Papers & Case Studies

71. Fumigation Within A Pharmaceutical Aseptic Filling Line

    Bioquell's Room Bio-Decontamination Service was required for a major multi-national pharmaceutical company needed a solution that woul removed Staphylococcus edpdermidis from specific zones in an aseptic filling line with areas ranging from European GMP Grade A to Grade D. The solution neeeded to meet FDS regulatory requirements and have proven efficacy documentation againt S. epidermidis.

72. Decontaminate A Pharmaceutical Production Facility In Less Than 24 Hours

    Bioquell's Room Bio-Decontamination Service (RBDS) was the only solution for the a major multinational pharmaceutical company that required their production lines within a European manufacturing facility to be sterilized in a short period of time.

73. Decontamination Comparison: Hydrogen Peroxide Vapor (HPV) vs. Ultraviolet Radiation (UVC)

    The fundamental differences between these technologies, in terms of their mode of antimicrobial action and the method of delivery, result in a marked difference in microbiological impact. Bioquell HPV eradicates pathogens on hospital surfaces and achieves a 6-log sporicidal reduction in vitro.

74. Hydrogen Peroxide Decontamination: Vapor Vs. Aerosolized Systems

    When facing a microbial contamination challenge, hether from multidrug-resistant organisms in a hospital or in bio-pharmaceutical production facilities, not all hydrogen peroxide-based decontamination systems are the same.

75. Variability In Sterility Test Processes And The Benefits Of Modular Workstations

    This paper reviews some of the current operational practices that incorporate sterility testing and provides an insight into the role of hydrogen peroxide vapor bio-decontamination and continuous particle monitoring. By James Drinkwater, Bioquell UK Process & Compliance Director

76. Factors To Consider When Selecting Bio-Decontamination Services

    RBDS or Room Bio-decontamination service is not only about the practical side of service delivery. By Yvonne Yeo

77. A Strategy For Implementing Rapid Microbial Methods

    The purpose of this white paper is to present a strategy to be used and applied for rapid microbiological methods (RMM). By Gilberto Dalmaso, Sterility Assurance Consulting, A&L Co

78. Surrogate Testing Of A Downflow Booth Complete With Integrated Tray Dryer

    Walker Barrier Systems was tasked with providing two downflow booths, each with integrated tray dryer (client provision) mounted in the side wall. The booth was to be used for filling trays with wet cake, as well as the dispensing of dried product from the trays into drums using a custom designed “tray dispensing hopper”.

79. Improve Efficiency In Bio-Contamination Control And Risk Mitigation

    There is a need to improve the efficiency in the pharmaceutical industry to meet new challenges of globalisation, competitiveness and the increasing diversity of products. By James Drinkwater

80. Biological Contamination Management In Aseptic Environments: Requirements And Expectations

    Bio-contamination found in critical zones within processing environments can affect the whole process and sterility of the final products, potentially putting patients at risk. This can lead to significant financial costs and impact operational resources. By James Drinkwater