Cleanroom Whitepapers and Case Studies
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Watermain Leaks Can Be A Costly Contributor In Energy Consumption And NRW Loss
2/10/2023
Mueller was hired by an energy performance firm to survey a federal government water distribution network in Ontario to determine if leakage was contributing to unnecessary energy consumption.
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CAR-T And Laminar Flow Glovebox Isolators
6/6/2024
A request was made for a containment system that would protect operators during lentivirus transfer, as well as provide a controlled environment for IL-2 charging of media, bead addition, and blood bag spiking.
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Robust, Scalable Strategy For Monodisperse Nanosuspensions Of Poorly Soluble Drugs
5/16/2025
By tailoring the formulation strategy, selecting the appropriate excipients, and fine-tuning process conditions, see how our team was able to improve bioavailability and in vivo exposure.
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Cell Collection Basics For The Transplant And CGT Industries
6/3/2025
Breakthroughs in CAR T-cell and stem cell therapies depend on mastering cellular collection. Understanding these fundamentals is vital for advancing treatment efficacy and patient outcomes.
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A Shift Towards Biofluorescent Particle Counters In Manufacturing
5/12/2025
Sterility in injectable drug manufacturing is vital for patient safety and efficiency. Discover how biofluorescent particle counters revolutionize contamination control, regulatory compliance, and operational excellence in modern pharma.
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Understanding Viral Clearance During Anion-Exchange Chromatography
3/26/2024
A design of experiments (DoE) study examined the anion-exchange process in general and to draw possible correlations between such properties and overall viral clearance capability.
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Compliance With Annex 1- Sterile Fill Finish
5/5/2025
Eurofins ensures Annex 1 compliance through robotic isolators, PUPSIT, contamination control strategies, and rigorous training for aseptic sterile fill-finish of early-phase clinical products.
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Perspectives On The Adoption Of Fully Closed Processing
1/16/2024
In this study, industry experts share their perspectives and plans related to the implementation of fully closed processing. Explore the drivers and challenges of fully closed processing and more.
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Mycoplasma Contamination In Biopharmaceutical Manufacturing
2/9/2024
Learn how strict laboratory practices and routine testing for mycoplasma contamination using nucleic acid-based assays can help ensure safe, high-quality biopharmaceutical products.
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A Streamlined Biopharmaceutical Isolator Solution
6/19/2024
This custom-designed, eight-foot isolator helped a client meet their decontamination needs, maintaining ISO-5 sterile conditions while decreasing turn-around time for filling small batches.