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Samsung Biologics Expands to 845,000L Capacity with GSK Facility Acquisition; Lonza, Resilience Announce Major Investments Amidst CDMO Restructuring

DCAT Value Chain Insights USA, South Korea, Switzerland
Overview
The CDMO industry is undergoing unprecedented restructuring in 2026, driven by major strategic investments and M&A activities by leading players. Samsung Biologics acquired a former GSK facility in Maryland for $353 million, expanding its global cGMP capacity to 845,000 liters, and plans to acquire PolyPeptide Group for $1.8 billion. Lonza continues a CHF 500 million investment in a large-scale commercial fill-and-finish facility in Switzerland, while Resilience expanded its partnership with Eli Lilly, investing $750 million in Ohio manufacturing operations. These moves underscore a critical industry-wide drive to bolster capacity and diversify supply chains to meet surging biopharmaceutical demand.
In Depth

Key Findings

In 2026, the Contract Development and Manufacturing Organization (CDMO) industry is experiencing significant strategic investments and acquisitions by major players, aimed at substantially expanding manufacturing capacity and strengthening supply chains. Notably, Samsung Biologics acquired a former GSK facility in Maryland for $353 million, which is projected to boost its global cGMP manufacturing capacity to an impressive 845,000 liters. Furthermore, Samsung Biologics has announced plans to acquire PolyPeptide Group, a leader in peptide therapeutics, for $1.8 billion, diversifying its modality portfolio.

Technical / Clinical Details

These investments are strategically addressing manufacturing bottlenecks across various biopharmaceutical modalities. Samsung Biologics’ capacity expansion is geared towards large-scale production of monoclonal antibodies and other recombinant proteins, contributing to the stabilization of the global biopharmaceutical supply. Lonza’s ongoing CHF 500 million investment in a commercial fill-and-finish facility in Switzerland aims to bolster sterile filling and packaging capabilities for final drug products, thereby reducing time-to-market. Resilience’s expanded partnership with Eli Lilly and its $750 million investment in Ohio manufacturing operations are focused on enhancing advanced manufacturing technologies and capacities in specific therapeutic areas, particularly gene and cell therapies. These state-of-the-art facilities are designed to maximize quality control and production efficiency, incorporating single-use bioreactors, advanced process automation, and data analytics systems.

Background & Context

The burgeoning biopharmaceutical pipeline, coupled with supply chain vulnerabilities exposed during the pandemic, has accelerated capacity expansion and technological innovation within the CDMO sector. Many biopharmaceutical companies are adopting a strategy of outsourcing substantial capital expenditures and complex manufacturing process management to CDMOs, allowing them to focus on core R&D. This shift has transformed CDMOs from mere manufacturing partners into comprehensive solution providers offering technical advice and regulatory strategy support from early development stages. The current moves by leading CDMOs reflect the overall industry growth trend, with an increasing focus on developing capabilities for next-generation modalities like cell and gene therapies, which are crucial for future competitive advantage.

Strategic Significance & Outlook

This active wave of investment and M&A in the CDMO industry is anticipated to continue. The cell and gene therapy sector, in particular, will likely see an even greater reliance on specialized CDMOs due to manufacturing complexity and high regulatory hurdles. Investments in advanced manufacturing technologies, such as continuous processing and AI-driven process optimization, are also expected to accelerate, leading to more efficient and cost-competitive biopharmaceutical production. This will enable pharmaceutical companies to concentrate more intensely on new drug development, ultimately expediting the delivery of innovative therapies to patients globally.

Source: https://www.dcatvci.org/features/cdmo-cmo-the-key-moves-in-2026/

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