Insights On Critical Environments
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Thermo Fisher Scientific Large Volume Liquid Expansion
5/2/2024
This video provides an insightful look into the expansion of the large volume liquids manufacturing site at the Grand Island facility, highlighting the various stages of the manufacturing process and the capabilities it offers to support the bioprocessing industry.
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New Vs. Used Processing Equipment: A Cost Comparison
5/9/2025
For pharmaceutical and chemical manufacturers, balancing budgets with operational needs is crucial. Discover how sourcing used equipment offers significant cost advantages over new.
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ISO/DTR 14644 -21 Cleanrooms And Associated Controlled Environments
2/22/2024
Here, we review the Technical Report outlining how particle counters are used to classify and monitor cleanroom performance, ensuring it meets required standards under normal operating conditions.
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Unstoppable Critical Cleaning To Increase Pharmaceutical Throughput
5/20/2024
Process optimization is key to achieving effective pharmaceutical and cosmetic critical cleaning. Learn how manufacturers can improve cleaning efficiency and ensure product safety.
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Selecting A Platform Filter For High Concentration mAbs
4/9/2025
Read more about how Fujifilm Diosynth Biotechnologies evaluated a prime filter with challenging simulant solutions and how the experimental data confirmed superior performance, which demonstrated twice the throughput.
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Scope 3 Emissions: Cut The Complexity With Creative Collaboration
11/20/2024
Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.
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A Mobile BSL-2 cGMP Cleanroom Delivered In Less Than 3 Weeks
6/6/2024
A mobile cleanroom facility was needed for manufacturing a new monoclonal antibody product for phase 1 clinical trials. The facility had to have the ability to be repurposed for additional applications.
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MilliporeSigma Bio-Expo Live February 2025: Downstream Bioprocessing
3/17/2025
Advancements in single-use technologies are transforming antibody-drug conjugate manufacturing and offering increased flexibility. Examine key data, design considerations, operational benefits, and applications in ADC production.
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Establishing Effective Visual Residue Limits In Cleaning Validation
10/23/2024
Learn about the technical nuances of Visual Residue Limits (VRLs) determination and explore strategies to implement robust VRL programs that meet regulatory standards and enhance manufacturing efficiency.
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Single cGMP Module: An Engineering Perspective
4/12/2024
Follow along on a tour through a recent Standard cGMP Module project. Germfree cGMP Modular Cleanrooms are a platform solution that unlock standalone manufacturing capacity for a variety of applications.