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| Outsourced Pharma Capabilities Update September 2026: Fill/Finish (Sept 1, 11am ET) | Explore the latest fill/finish capabilities from leading CDMOs, including sterile filling, lyophilization, and advanced packaging. This session highlights available capacity, global facilities, and timelines to support your development and manufacturing needs. Learn how quality control and regulatory compliance ensure product integrity, with concise presentations designed to help biopharma teams connect with partners and make informed outsourcing decisions. Learn more. |
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By Jeffrey S. Buguliskis, Ph.D., deputy chief editor, Outsourced Pharma | Just like inspecting a house before a major renovation, biopharmas must address underlying bispecific structural and analytical flaws before handing their molecule off to a CDMO. | |
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INDUSTRY INSIGHTS CONTINUED |
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| Optimizing Bioavailability With Predictive Science | Case Study | Thermo Fisher Scientific | In silico modeling cut through formulation guesswork for a compound with 0.015 mg/mL solubility, delivering an 8× Cmax and 5× AUC improvement and Phase I progression. |
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OUTSOURCED PHARMA CAPABILITIES UPDATE |
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CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs. |
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| Connect With Outsourced Pharma: |
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