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Webinar: Using Residual DNA Quantification Data to De-risk mAb Development
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IND-stage analytical methods must support validation, tech transfer, and evolving regulatory expectations. In this webinar, learn how residual host cell DNA quantitation can guide downstream mAb process decisions, assess impurity clearance, and identify risks early. Explore assay performance in protein-rich matrices and strategies for building scalable, validation-ready workflows that remain robust through manufacturing and commercial production environments globally. Click here to learn more.
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Webinar | MilliporeSigma
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Learn about best practices for cell bank manufacturing, how to get the most out of your cell bank, the future of closed processing in line with Annex 1, and more.
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Video | Thermo Fisher Scientific Bioproduction
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Master the essentials of single-use assembly design. See how a step-by-step configurator with 3D renderings simplifies fluid management.
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Video | Bioprocess Online
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In this segment from the Bioprocess Online Live event, panelists Moiz Diwan, Ph.D. (AbbVie), and Kat Kozyrytska (independent technology consultant) agree that collaboration across the industry is the quickest way to make meaningful progress with today’s technologies.
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Video | Bioprocess Online
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In this episode of "Better Biopharma," host Tyler Menichiello is joined by BioPlan Associates’ director of research, Katrina Cordovado, as well as Joshua Nelson, Ph.D., a senior material qualification specialist at Takeda, and Paul Priebe, a consultant and single-use expert, to continue their conversation from the Bioprocess Online Live event, "Closing The Adoption Gap For Advanced Single-Use Materials."
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Webinar | AES Cleanroom Technology
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ISO classification decisions shape cleanroom design. Find out how early alignment between process needs, biosafety, and classification can reduce redesign risk while supporting scalable environments.
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Webinar | Repligen
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High‑concentration mAbs change how UF/DF behaves. Discover how modern TFF platforms help address these challenges and maintain control as formulations move beyond traditional limits.
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