Newsletter | August 25, 2025

08.25.25 -- Discover Large Molecule CDMOs With Available Capacity

Considering outsourcing development and manufacturing? The Outsourced Pharma Capacity Update (OPCU), a free, interactive, digital event, convenes the industry's foremost CDMOs to provide up-to-date and direct insights into their available capacity and services, alongside specific facility and equipment updates. 

 

Discover the July 2025 event’s presenting sponsors in this newsletter to learn how they are best suited to help you to navigate the path to approval and commercialization.

LARGE MOLECULE DRUG SUBSTANCE & DEVELOPMENT

Aragen

Aragen’s newly built cutting-edge biologics manufacturing facility launches with GMP capabilities from 50L to 2000L with a DP filling line and ADC conjugation suite set to redefine bioproduction in India.

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Aragen

FUJIFILM Biotechnologies

Explore the strategic application of extensive expertise in microbial systems to meet increasing demand. Cutting-edge capabilities ensure streamlined development and manufacturing processes.

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FUJIFILM Biotechnologies

Cytovance Biologics

Thomas Kohl, Director of Business Development, shares microbial and mammalian capabilities and available capacity. Cytovance delivers ingenuity end-to-end to both large pharma and biotech clients.

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Cytovance Biologics

Novartis Contract Manufacturing

Review biologics CDMO solutions and capacity offered by Novartis Contract Manufacturing. Review capabilities in mammalian cell culture manufacturing and microbial fermentation.

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Novartis Contract Manufacturing

Resilience US, Inc.

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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Resilience US, Inc.

ADC

Lonza

Leveraging Lonza's deep ADC expertise and experience, successfully develop high quality, commercially viable processes, spanning from pre-clinical development through commercial scale manufacturing.

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Lonza

MilliporeSigma

With more than 15 years of experience as conjugation and linker-payload CDMO, MilliporeSigma has a proven track record of supporting clinical programs from IND to PPQ for commercialization.

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MilliporeSigma

Simtra BioPharma Solutions

With more than 65 years of sterile injectable manufacturing experience, Simtra offers world-class GMP sterile fill/finish services, deep scientific and technical expertise, and a uniquely collaborative approach.

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Simtra BioPharma Solutions

EVENT REGISTRATION

Streamline your search for the ideal CDMO partner at the October 2025 OPCU virtual event! Ease the burden of a prolonged vetting process by connecting with multiple CDMOs to find the best partner for your project while getting an inside look at their capabilities and capacities.

 

Monday, October 6: Analytical Services

Monday, October 6: ADC

Tuesday, October 7: Large Molecule

Wednesday, October 8: Small Molecule Drug Substance/API

Wednesday, October 8: Small Molecule Drug Product/Finished Dosage Form

Thursday, October 9: Cell & Gene Therapy

Friday, October 10: Fill/Finish