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  • Testing Aseptic Packaging
    The aseptic package is only as good as the final sealinq of the ingredients. A small amount of inert gas is injected into a package of dairy and meat products to ensure freshness.
  • Aseptic Processing, the Japanese Way
    By Jim Akers, Akers Kennedy and Associates, Kazuhito Tanimoto, Shibuya Kogyo Co., Ltd., and Masahito Kawata, Handai Biken While the global pharmaceutical industry tends to be conservative in nature, its implementation of newer technologies for aseptic processing has been impressive and nowhere
  • Aseptic Processing, the Japanese Way
    Operational Excellence & Lean Six Sigma Akers, J.E., M. Kokubo and Y. Oshima. "The Next Generation of Aseptic Processing Equipment. " Aseptic Processing Supplement to Pharmaceutical Technology U.S. Food and Drug Administration. Guidance for Industry: Sterile Drug Products Produced by Aseptic
  • What is Advanced Aseptic Processing?
    performing it would be important concerns. It is not clear to what extent a major line clearance might be required, and what subsequent interventions might be required to restore the system to operation. Clearly, aseptic systems that use gray- or black-side maintenance come closer to the spirit
  • What is Advanced Aseptic Processing?
    By James Agalloco, James Akers and Russell Madsen Over the last few years the term advanced has been applied to a number of aseptic manufacturing technologies. The 2002 open conference on sterile products co-sponsored by USP and PDA made advanced aseptic processing a discussion point
  • Robotics in aseptic drug manufacturing.
    They key to Advanced Aseptic Processing. is absolute control of all sources of contaminants,. most importantly the human. element. Robotics and isolator-barrier. systems are core technologies in this regard. A properly integrated robot system. combined with an isolator-barrier system. offers
  • Aseptic Processing, the Japanese Way
    particulate contamination, which would be considered significant in an ISO Class 5 environment. In fact, studies have determined that they would be suitable for use in an ISO Class 4 environment. These robots were co-developed by Shibuya Kogyo Co. Ltd. and Fanuc Robotics specifically for use in aseptic
  • What Makes a Room Suitable for Aseptic Processes?
    Biological contaminants are ubiquitous. Microorganisms such as bacteria or fungi roam free in most environments and can cause disease. A major goal of aseptic applications, including surgery, pharmaceutical compounding or medical implant packaging is to prevent contaminants and the potential
  • From Drinks to Drugs: A Proposal for Advancing Aseptic Processing and Eliminating Contamination Risk
    By Dr. James E. Akers, Akers Kennedy Associates, and Yoshi Izumi, Shibuya Hoppmann Corp. For most of the last three decades, there has been a tacit understanding that one simply had to accept some level of contamination in any aseptic processing environment. The reasons for this begrudging
  • From Drinks to Drugs: A Proposal for Advancing Aseptic Processing and Eliminating Contamination Risk
    By Dr. James E. Akers, Akers Kennedy Associates, and Yoshi Izumi, Shibuya Hoppmann Corp. In the beverage industry, there is no debate at the present time regarding aseptic manufacturing environments. All such environments are separative enclosures similar if not identical in all respects to what

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  • The intensive medicine
    - The prevention of the V. femoralis, Daily review, of the indication position, skin disinfection, with chlorhexidine / alcohol standardized the aseptic installation or Octenidin / Alkohohl (remanence effect) Infektionssurveillance, personal trainings .
  • Microbiological traineeship
    A sterile solution or a sterile apparatus is disinfected therefore also automatically whereas a disinfection nor no sterility represents.
  • Prevention of katheterassoziierter infections
    Because of this risk, the same aseptic installation conditions are asked for the installation on the described focalizations like for the installation of a ZVK.
  • Prevention of katheterassoziierter infections
    Because of this risk, the same aseptic installation conditions are asked for the installation on the described focalizations like for the installation of a ZVK.
  • Encyclopedia of Industrial Biotechnology: Bioprocess Bioseparation and Cell Technology 7 Volume Set
    � water lines are usually constructed of schedule 80 plastic PVC (1�2 pipe) which delivers the deionized water to tanks where it is batch-sterilized or else transferred to a stainless steel piped sterilizable filter unit to be sterile-filtered into aseptic equipment .