Facility Design Webinars
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PUPSIT Without The Pain: Practical Solutions For Implementation
5/6/2025
Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.
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White Raven's Accelerated Path To GMP Certification
4/28/2025
CDMO White Raven achieved GMP certification using an innovative aseptic filling solution in just 18 months. Discover how meticulous planning and collaboration set a new industry standard for efficiency.
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Why Internal Manufacturing Is Key To Meira GTx's Success
4/23/2025
CEO Zandy Forbes shared Meira’s origin story and how building an in-house manufacturing facility allows the company to develop an expansive pipeline of gene therapies.
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Sustainable Manufacturing Through Efficient BioProduction Unit Operations
4/23/2025
Delve into the critical environmental and economic aspects of bioprocessing. Explore the urgent need to manage the industry’s growing plastic waste issue and a three-pronged approach to address this challenge.
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Overcoming Facility Constraints Posed By Process Intensification
4/14/2025
Discover how your facility's layout and process flow might limit its potential and learn about media requirements in USP and DSP to optimize your scheduling and footprint for efficient media management.
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An Unrivaled Modular Seed Train For Process Intensification
4/14/2025
Listen to experts as they discover a modular, perfusion-enabled seed train system and learn about the time benefits, cost benefits, and scalable process development for various production needs.
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Meeting Demand For Enhanced Cleaning Protocols While Reducing Bioburden
3/31/2025
Intensified cleaning protocols are vital for drug purity, yet strain conventional protein A resins. Discover how a novel resin, engineered for robust caustic resistance, ensures longevity and efficiency gains.
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Do Not Bear Cross Contamination In The Pharmaceutical Industry – Prevent It
3/25/2025
Learn how thorough cleaning and process optimization in pharma manufacturing prevent cross-contamination, ensure product integrity, and enhance efficiency while also improving compliance and reducing costs.
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CARR Biosystems Bio-Expo Live February 2025: Downstream Bioprocessing
3/17/2025
Discover a single-use centrifuge system, made by a company with 30+ years in cell culture separation, that excels in scaling across various modalities and cell types to optimize workflows.
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Downstream Purification Strategies And Solutions For Biotherapeutic Molecules
3/17/2025
With 25+ years of experience in research and development, watch a Process Chromatography Support Scientist guide clients in chromatographic purification, protein production, cell therapy, and GMP manufacturing.