Insights On CONTRACT PHARMA MANUFACTURING
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Amorphous Solid Dispersions: Pre-Clinical To Commercial Capabilities
7/29/2025
ASDs are an attractive option for commercializing poorly soluble compounds. This talk focuses on capabilities to screen the potential for ASDs in early phase studies and their commercial applicability.
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Your Integrated Drug Substance Partner
7/29/2025
With capabilities to support your next small molecule drug substance program from R&D to commercial scale, learn about our integrated facilities, project teams, and available capacity.
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Management Strategies For Adaptive Bio And Single-Use Excellence
7/28/2025
Single-use technologies (SUTs) bring speed and flexibility to modern biomanufacturing, but realizing their full value requires robust, stage-specific risk management to navigate material, supply chain, and regulatory challenges.
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Drug Product Development Of Poorly Soluble Compounds
7/28/2025
Eurofins CDMO Alphora offers comprehensive drug product development and manufacturing, specializing in poorly soluble compounds, clinical manufacturing, and integrated solutions for diverse clients.
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Aragen Capacity Update July 2025: Small Molecule Drug Substance/API
7/28/2025
Explore specialized expertise in solving challenging small molecule formulation problems (poor solubility, bioavailability, complex delivery routes).
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Resilience Capacity Update July 2025: Large Molecule Drug Substance
7/28/2025
Hear from Evan Pasenello, Head of Commercial Services, about how Resilience can support large molecule programs from early phase through clinical and commercial manufacturing.
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Novartis Contract Manufacturing Capacity Update July 2025: Large Molecule Drug Substance
7/28/2025
Review biologics CDMO solutions and capacity offered by Novartis Contract Manufacturing. We discuss our capabilities in mammalian cell culture manufacturing and microbial fermentation.
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FUJIFILM Biotechnologies Capacity Update July 2025: Large Molecule Drug Substance
7/28/2025
Review the strategic application of extensive expertise in microbial systems to meet the increasing demand for novel biologics. Cutting-edge capabilities ensure streamlined development and manufacturing processes.
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Cytovance Biologics Capacity Update July 2025: Large Molecule Drug Substance
7/28/2025
Thomas Kohl, Director of Business Development, shares the company’s microbial and mammalian capabilities and their available capacity. Cytovance delivers ingenuity end-to-end to both large pharma and biotech clients alike.
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Aragen Capacity Update July 2025: Large Molecule Drug Substance
7/28/2025
Aragen’s newly built cutting-edge biologics manufacturing facility launches with GMP capabilities from 50L to 2000L—scaling to 5000L soon—with a DP filling line and ADC conjugation suite set to redefine bioproduction in India.