INSIGHTS ON FACILITY DESIGN
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Thermo Fisher Scientific Large Volume Liquid Expansion
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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Get To Know WuXi Advanced Therapies Testing Services
Learn how we can help you move your pipeline forward, whether you manufacture with us at WuXi Advanced Therapies, in-house, or with one of our fellow CDMOs.
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Single-Use Microbial Impactor On A Filling Line
Discover the advantages of a single-use microbial impactor through a demonstration of its ease of use in an isolator and an explanation of its ability to eliminate false positives.
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How Airflow Visualization Characterizes Pharmaceutical Sterility
Explore how airflow visualization studies influence contamination control and risk management in pharmaceutical environments.
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ISO/DTR 14644 -21 Cleanrooms And Associated Controlled Environments2/22/2024
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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Understanding ISO/TR 14644-21 Airborne Particle Sampling Techniques2/22/2024
Industry expert Mark Hallworth guides viewers through the latest ISO document (ISO 14644), exploring the reasons behind the decisions made by the team during its development.
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EMPQ And Validation Support Services2/21/2024
A growing pharmaceutical/biotech company hired a global consulting firm for a project that required EMPQ services for qualification activities on a newly completed aseptic processing suite.
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SAP S4HANA Implementation: Commissioning, Qualification, And Validation2/20/2024
Explore how CAI helped one company navigate complications when implementing SAP and how new solutions are being developed, validated, and implemented to establish this new global ERP system.
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Consolidating The Supply Chain For mRNA2/12/2024
Learn about the first end-to-end cGMP facility that was developed for mRNA manufacturing to address the shortage of CDMOs and the inadequate and inefficient supply chain options for sourcing GMP mRNA.
FACILITY DESIGN SOLUTIONS
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Discover aseptic sampling solutions designed to seamlessly integrate with stainless steel processes and collect perfectly representative samples at every process step and scale without false-positives.
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By streamlining the synthesis pathways, see how these products can effectively diminish the requisite number of developmental and manufacturing stages essential for generating payloads.
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Explore a portfolio of best-in-class detergent alternatives to Triton™ X-100 for use in biomanufacturing applications.
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Experience Unparalleled Cleanliness and Speed
At AES Clean Technology, we understand the critical importance of maintaining ultra-clean environments in industries such as pharmaceuticals, biotechnology, medical device, high tech manufacturing, and more. That’s why we’re proud to introduce the CleanLock Module™ – a revolutionary airlock solution designed to enhance cleanliness, speed, and efficiency in your cleanroom project execution.
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Review how a comprehensive cGMP manufacturing facility is poised to support the development and manufacture of your mammalian cell program.