Pharmaceutical Clean Rooms

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  • Isolator Systems Take On Clean Rooms
    What's smaller than a clean room, cooler than a glovebox, and able to leap any aseptic standard in a single bound? It's Super-Barrier, better known as the isolator system. In its Technical Report 34, Design And Validation Of Isolator Systems For The Manufacturing And Testing Of Health Care Products
  • Isolator Systems Take On Clean Rooms
    is expensive given energy consumption, equipment, air filtration, gowning and difficulty working in such environments. In pharmaceuticals, the trend has been away from larger classified space toward maintaining ultra-clean stations wherever appropriate. "It makes much more sense for pharmaceuticals to have
  • Monitoring Provides Process Validation in the Pharmaceutical Industry
    Process validation in the pharmaceutical industry is critical; physical or chemical changes in medications can result in the loss of their effectiveness. Hence, rigorous and adequate temperature and humidity control in pharmaceutical industry environments, such as laboratories and clean rooms
  • The Use of Optical (Chilled Mirror) Sensor Technology for Moisture Measurement
    to calibration and metrology laboratories, these applications include clean rooms, pharmaceuticals, fuel cell research, R&D, and furnaces.
  • Interphex Preview, Part Deux
    the planning and design of facilities, clean rooms, HVAC systems, central utility plants, and distribution systems for advanced manufacturing and healthcare institutions. High-Tech Instruments for Life Sciences offers instruments, scientific equipment and integrated software solutions. Products
  • What to Expect at Interphex 2007
    needs. Cashco offers a full line of sanitary regulators and control valves solutions for pharmaceutical applications. ( Dwyer Instruments, Inc. is featuring its new Digihelic II Differential Pressure Controller, which is suited for monitoring pressures in clean rooms or containment zones
  • Extending the Validated Workplace
    Production typically involves mixing active pharmaceutical ingredients into solution, while another part of the plant produces IV bags and closures, Collins says. The two come together in filling stations in clean rooms, and the finished products are then steam-sterilized. Regulatory compliance
  • Extending the Validated Workplace
    or through alliances with other vendors. Here, too, though, questions about whether activities are regulated or non regulated have crept in. Many validated facilities put strict controls on access to clean rooms, for example, and thus records on who entered such rooms can become a part of the

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