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| Webinar: Bacterial Retention Testing Explained: Demonstrating Filter Performance For Your Product | How do you demonstrate that sterilizing filters perform as intended? Join Alcami to explore bacterial retention testing, including the role of Brevundimonas diminuta, the impact of product and process conditions, and how filter integrity testing supports validation. Gain practical insights into planning bacterial challenge studies, interpreting results, and aligning testing strategies with product requirements and sterile manufacturing needs. Click here to learn more. |
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Video | Abzena | Accelerate biotherapeutic development with integrated workflows. Learn how early stable pools and advanced vectors decouple material generation from clone selection, de-risking clinical scale-up. |
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Webinar | KBI Biopharma | Particle contamination risks biologic safety. Advanced tools like Raman and SEM-EDS identify root causes fast to support robust, regulator-ready strategies that protect product quality. |
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Webinar | Adare Pharma Solutions | Explore 3D screen printing’s potential to revolutionize pharmaceutical manufacturing with scalable, customizable, multi-drug tablets and precise, patient-centric drug release profiles. |
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Webinar | Upperton Pharma Solutions | A fireside chat explores spray drying for nasal biologics, covering formulation science, particle design, delivery advantages, and testing strategies to move from concept to clinic. |
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Video | Bioprocess Online | During this final segment from the Bioprocess Online Live event, “Making The Jump To GMP: Material Decisions For Clinical Manufacturing,” a representative and SME from the event sponsor enters the conversation. Mike Brewer, director and global principal consultant of regulatory and bioproduction at Thermo Fisher Scientific, joins the panel for a special Q&A session with the audience, discussing the challenges he’s witnessed sponsor companies face in the transition to clinical manufacturing. |
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Video | Morpho Alfasigma | Food and supplement manufacturing in Louisiana spans blending, compression, film coating, encapsulation, and several packaging formats, backed by dedicated quality control testing from raw materials through finished product. |
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Video | Eurofins | Advance pharmaceutical quality and sustainability by adopting recombinant factor C testing for reliable, animal-free endotoxin detection. |
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| Webinar: Planning For Scale From The Start: Where Early Development Decisions Create Commercial Risk | Commercialization challenges often start long before commercial manufacturing. This Catalent webinar explores how emerging biopharma companies can connect development, manufacturing, quality, and supply planning earlier to prepare for future demand, reduce scale-up and technology transfer risk, and strengthen launch readiness. Learn how an accelerated, connected approach can build greater supply resilience as programs progress toward commercialization. Click here to learn more. |
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