Cleaning, Sterilization & Bio Decontamination White Papers & Case Studies

31. Decontamination Of Laboratory Animal Research Rooms Using Vaporized Hydrogen Peroxide (VHP®) 4/12/2012
    Walter Reed Army Institute for Research is a U. S. government laboratory facility located in the Washington D.C. area.
32. Biomanufacturing Debottlenecking And Process Optimization 3/6/2012
    Optimizing biomanufacturing is particularly challenging because of variability and complexity associated with the sharing of finite and interdependent resources. By BIO-G
33. Turning Data Into Information 12/22/2011

    As biopharmaceutical manufacturing has evolved from small-scale lab production in small flasks to massive commercial production in deep-tank bioreactors, an avalanche of production data has evolved to support it. From individual unit operation skids to distributed control systems and enterprise resource planning tools, biomanufacturing today is buried by the sheer quantity of data coming in from the manufacturing floor.

34. Crucial Questions To Ask Before Outsourcing Your Stability Storage 11/8/2011
    There’s overwhelming evidence that says now, more than ever, is the right time to get ahead of the game by outsourcing your stability storage needs to Vindon Scientific (USA) Inc.
35. Sterile Drug Products Produced By Aseptic Processing — Current Good Manufacturing Practice 7/28/2011

    This guidance is intended to help manufacturers meet the requirements in the Agency's current good manufacturing practice (CGMP) regulations (2l CFR parts 210 and 211) when manufacturing sterile drug and biological products using aseptic processing. By PharmaSystems, Inc.

36. White Paper: Production Of Prefilled Syringes 6/16/2011
    The production and the filling of prefilled syringes is a process that comprises a lot of single steps: first the syringe has to be manufactured out of glass tubes. After that the syringes have to be cleaned, sterilized, and siliconized. By Dr. Wenzel Novak
37. Case Study: Marchesini Group for Catalent Pharma Solutions: Efficient Syringe Packaging 5/4/2011
    To meet the requirements of efficiency and flexibility for packaging pharmaceuticals that are rather difficult to process is a challenge that the American pharmaceutical group Catalent Pharma Solutions has won alongside Marchesini Group.
38. White Paper: Utilizing InfoBatch To Generate Clean-In-Place (CIP) Reports 4/22/2011
    Many sterile manufacturing facilities find it difficult to manage Clean-in-Place (CIP) reports and are searching for a solution. InfoBatch is a flexible electronic batch reporting application that can be configured to create and maintain CIP reports for manufacturing facilities. By Informetric Systems Inc.
39. Selection Of Cleaning Agents And Parameters For CGMO Processes 1/27/2011

    Selecting suitable cleaning agents and determining justifiable cleaning process parameters are critical prerequisites for cleaning validation. Proper selection of these cleaning agents and parameters could simplify cleaning validation efforts immensely.By STERIS Corporation

40. The Design And Testing Of A Continuous Effluent Sterilization System For Liquid Waste 12/22/2010
    The disposal of microbiologically contaminated or potentially contaminated liquid waste is an important consideration for research facilities and other installations. This report describes a new continuous effluent decontamination system that allows for the continuous collection, thermal sterilization, and cooldown of wastewater prior to discarding from the facility. By STERIS Corporation