Insights On Facility Design
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Key Elements Of Process, Analytical Development To Support Tech Transfer
5/13/2024
Tech Transfer for biologic medicinal products is complex - filled with potential pitfalls, hazards, and breakpoints. Review strategies and methodologies for seamless technology transfer to your CDMO.
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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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Get To Know WuXi Advanced Therapies Testing Services
3/21/2024
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
3/6/2024
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
2/22/2024
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 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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Understanding ISO/TR 14644-21 Airborne Particle Sampling Techniques
2/22/2024
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 Services
2/21/2024
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 Validation
2/20/2024
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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Prove A Sterility Assurance Level Of 10⁻⁶
2/13/2024
Explore the Biological Indicator/Bioburden (BI/BB) method for achieving sterilization of products along with the prerequisite studies needed to develop the sterilization process.