Cleaning, Sterilization & Bio Decontamination White Papers & Case Studies
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Improving Uptime In Aseptic Processing Of Pharmaceutical Liquids
10/17/2018
Maximized uptime, minimized changeover time, and efficient OEE are key factors that have influenced the acceptance of aseptic blow-fill-seal in the packaging of pharmaceutical liquids.
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Aseptic Blow/Fill/Seal Technology vs. Traditional Aseptic Processing
10/17/2018
Learn why blow-fill-seal technology has been gaining increasing worldwide acceptance in the parenteral drug marketplace, replacing traditional glass vial processing in a growing number of applications.
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Aseptic Blow-Fill-Seal: A Sustainable Process For Packaging Pharma Liquids
10/17/2018
Aseptic blow-fill-seal systems for packaging pharmaceutical liquids incorporate materials and processes that provide critical advantages for sustainable initiatives.
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Mixing Technologies In The Pharmaceutical And Medical Industries
3/1/2018
Mixing equipment employed in the production of pharmaceuticals and medical devices deal with a higher level of complexity because their use is more specialized. Not one design fits all.
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Maximizing Contamination Control With Vacuum Technology
2/13/2018
For the 50 or so years that cleanrooms have been in use, a steady debate has centered on the best ways to keep them clean, and regulatory and advisory agencies have weighed in on maintenance.
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Isolator Advantages in Cell Therapy Production
11/15/2017
Cell and gene therapies are currently produced in fixed facilities that require a significant upfront investment. Modular concepts offer an opportunity to shift from these large, fixed assets.
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Blow-Fill-Seal For Biologics: Breaking Through In Pharma Packaging
5/3/2017
As the industry continues its move toward biologics, innovative solutions and technologies will be needed to ensure a safe and reliable approach to the manufacturing and delivery of these drugs.
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High-Potency Containment For Polypeptide Vaccine Manufacturing
4/5/2017
The team at Polypeptide Labs' overall project aim was to achieve homogenization (blending/tumbling) of potent lyophilized polypeptide product offloaded from a separate isolator.
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Optimizing Your Critical Cleaning Process To Ensure Results
2/2/2017
Getting the best results from any cleaner requires proper mixing and cleaning procedures. This article includes mixing directions for aqueous cleaning detergent and methods for monitoring performance.
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Cleaning Validation For Medical Device Manufacturing
2/2/2017
Cleaning validation or verification is a necessary regulatory compliance step in medical device manufacturing and reprocessing. Support from the cleaner manufacturer can save time and money.