Cleaning, Sterilization & Bio Decontamination White Papers & Case Studies
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Biodecontamination Of Animal Rooms And Heat-Sensitive Equipment With Vaporized Hydrogen Peroxide
4/12/2012
Common methods used to decontaminate and disinfect laboratory animal areas are difficult to standardize, labor-intensive, and potentially hazardous for staff members and the environment.
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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.
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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
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Bacteria May Avert Radioactive Waste Problems
1/11/2012
Saxony and Thuringia are mountainous German states featuring quaint villages, carved nutcrackers and centuries-old castles. But there is another side to this region.
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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.
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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.
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OSHA Laboratory Standard
11/1/2011
Part 1910-Occupational Safety And Health Standards
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Development Of The Labconco Protector® XStream® High Performance Laboratory Fume Hood
8/3/2011
Safety is the primary purpose of any laboratory hood. Facility managers and laboratory planners desire fume hoods that can conserve energy without compromising safety.
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Case Study: NANOSAFE TESTED™ Summary
8/3/2011
NanoSafe, Inc. developed a testing program to independently evaluate the generation and containment of a controlled nanoaerosol inside a Labconco XPert® Nano™ System.
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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.