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| Join this Outsourced Pharma Live discussion: Charting a Direct Pathway from Academia To CDMOs on August 4, 2026 to learn how academic innovators, technology transfer offices, and CDMOs can bridge critical gaps in documentation, quality expectations, and development strategy. Hear practical advice on creating stronger technical packages, aligning earlier with CDMO partners, and accelerating the path from promising research to real-world manufacturing success. Register. |
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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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Video | AGC Biologics | With multiple cGMP manufacturing lines, a flexible uni-flow design, and cutting-edge single-use technologies, the site delivers speed, scale, and compliance for both mammalian and microbial biologics. |
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Webinar | KBI Biopharma | A bottom-up, data-driven media design approach shows how nutrient optimization overcomes metabolic limits to boost culture performance and titer while maintaining product quality and process consistency. |
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Video | West Pharmaceutical Services, Inc. | Struggling to keep pace with EU GMP Annex 1? The right supplier partnership brings regulatory insight your team may be missing. Assimilate how strategic collaboration closes compliance gaps and prepares you for future regulations. |
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Video | Outsourced Pharma | This segment of the Outsourced Pharma Live event, “Beyond Data Packages: De-Risking Tech Transfer To CDMOs,” examines where sponsor data packages most often fall short, including assumptions that equipment, raw materials, water systems, hold times, sampling methods, and undocumented process adjustments will transfer cleanly. |
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Video | Eurofins | Discover how advanced sequencing and bioinformatics technologies are helping shape the future of viral safety assessment in biopharmaceutical manufacturing. |
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| Connect With Outsourced Pharma: |
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