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Moving into GMP manufacturing can bring costly challenges—from sourcing and validating materials to regulatory compliance, risk assessment, and facility fit. Join Bioprocess Online’s Tyler Menichiello and industry experts Wei Lu, Ph.D., Tiffany Rau, Ph.D., and Mary Rodley 9/18/26 at 11 AM ET for an interactive panel on phase-appropriate CMC decisions and material selection. Discover key considerations for implementing GMP-grade materials and equipment while preparing your process for successful clinical manufacturing. Register today!
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Video | MilliporeSigma
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Discover a faster, more sensitive approach to rodent virus detection that offers a targeted NGS workflow to help uncover contaminants traditional assays may miss.
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Video | Thermo Fisher Scientific
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Single-use bioreactors with turndown ratios up to 20:1 enable facilities to operate across wide volume ranges.
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Video | Bioprocess Online
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In this episode of “Better Biopharma,” host Tyler Menichiello is joined by Deck Bio’s CSO, Johanna Kaufmann, to discuss the company’s multi-peptide-MHC-targeted T-cell engager platform for solid tumors.
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Video | Agilent Technologies
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Combining denaturing and native analytical techniques reveals molecular weight impurities in mAbs, delivering a more complete and reliable purity profile that supports confident decisions.
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Webinar | IDBS UK HQ
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Bridge the gap between lab speed and scientific confidence. Learn to eliminate operational bottlenecks, ensure material readiness, and create the traceable data needed for an AI-ready future.
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Video | CellBri
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Rigorous multi-cycle stress testing and environmental validation ensure manufacturing hardware delivers uncompromising reliability for critical processing workflows.
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