Containment & Isolation White Papers & Case Studies
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Improve Efficiency In Bio-Contamination Control And Risk Mitigation
There is a need to improve the efficiency in the pharmaceutical industry to meet new challenges of globalisation, competitiveness and the increasing diversity of products. By James Drinkwater
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Biological Contamination Management In Aseptic Environments: Requirements And Expectations
Bio-contamination found in critical zones within processing environments can affect the whole process and sterility of the final products, potentially putting patients at risk. This can lead to significant financial costs and impact operational resources. By James Drinkwater
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5 Questions To Ask Yourself Before Purchasing A Containment System
If you are considering purchasing a containment system, here are five questions to answer that will help you prepare before contacting or working with a containment system vendor.
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Facing The Challenges: Single-Use Approaches To Powder Transfer
Media and buffer preparation is a key part of the biopharma manufacturing process. Improving the powder transfer process makes this step cleaner, safer, more efficient,and reduces costs.
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Benefits And Risks Of (UV) Ultraviolet Radiation
Soon after the discovery of microorganisms, biologists began to observe that many varieties of these creatures were able to be incapacitated by exposure to sunlight. Following the discovery of the ultraviolet bandwidth in 1801, scientists attributed the sun’s lethal effect to this invisible energy. Facilitated by the findings of a large body of experimental evidence collected in the decades following these initial hypotheses, contemporary scientists have determined that nearly all bacterial activity can be eradicated or at least attenuated by some wavelength of ultraviolet energy.
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Flexible Containment Solutions Guide: Drum Transfer System
Flexible Containment for offloading drummed materials in a safe and efficient manner is provided by the Drum Transfer System (DTS) platform. The DTS consists of an enclosure attachment frame, a support stand, a drum lifter, an enclosure, an outer drum sleeve, and discharge softgoods that are dependent upon your process equipment.
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Particle Testing in Cleanroom High-Pressure Gas Lines for ISO 14644
This paper provides guidelines for the testing of high pressure gases used in cleanrooms according to the cleanliness limits derived from the ISO 14644-1 cleanroom classification standard, the FDA cGMP guidelines and the EU GMP Guidelines. Specifically, this applications paper relates to satisfying the air particle concentration limits of Class 100 (ISO 5) where product is exposed to the air environment.
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Flexible Containment Solutions Guide: Document Transfer Enclosure
The Flexible Document Transfer Enclosure is designed to allow paperwork used in pharmaceutical processing to be handled in a contained way so that powders are not transferred onto the documents and to areas or individuals that are not protected. Submitted by ILC Dover
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Continued Process Verification Methods In Cleaning Validation
An increasing interest in continued process verification has led to the spread of on-line assay methods in cleaning processes. This paper deals with two different on-line applications: conductivity sampling and the Total Organic Carbon analysis for washing machines.
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Innovative Valve Interfaces Ensure Customized Productivity In B. Braun LIFE Nutrition Plant
B. Braun Melsungen AG is one of the leading companies in the international pharmaceutical and medication sector. With an investment of 164 million Euros the company is currently building the LIFE Nutrition plant, one of the world’s most modern production sites for innovative nutrition solutions, at the company headquarters in the North Hessian city of Melsungen. Jens Voigtländer, Editor