Pharma Manufacturing Evolves: CDMOs Drive Growth with Specialized Expertise and Tech-Driven Partnerships

September 13, 2026
Pharma Manufacturing Evolves: CDMOs Drive Growth with Specialized Expertise and Tech-Driven Partnerships
  • The industry is shifting from broad capacity expansion to specialized, technology-driven partnerships that emphasize deep expertise in biologics, peptides, high-potency drugs, ADCs, and cell/gene therapies.

  • AI and digital manufacturing are becoming integral, enabling faster development timelines, predictive quality control, and digital twins to optimize processes and troubleshoot issues.

  • The biologics CDMO market is dynamic, expected to grow from about $32.2 billion in 2025 to roughly $103.1 billion by 2035 as complexity and regulatory demands rise.

  • Across the globe, the CDMO market is expanding rapidly—projected to reach about $369 billion by 2034 from a 2025 baseline near $197 billion—driven by demand for biologics, peptides, ADCs, and advanced therapies.

  • Future leaders will blend scale with specialized expertise, regulatory excellence, and close customer collaboration, making CDMOs central to pharma innovation and resilience.

  • Pharmaceutical manufacturing is shifting from in-house production to integrated CDMO partnerships spanning development, clinical manufacturing, and commercial production.

  • Drivers of the CDMO wave include localization pressures, tariff and supply-chain considerations, easier financing, and a shift toward depth-focused capabilities rather than broad end-to-end services.

  • Technology transfer between lab and commercial scales remains a challenge, underscoring the need for robust digital analytics, real-time data sharing, and disciplined capacity management to avoid overcapacity.

  • Investments are flowing into regionalized, technology-intensive capacity, with notable commitments such as Lilly/Resilience funding for US device manufacturing, Evonik expansion, and several new or expanded facilities for peptide and biologics work.

  • Smaller and virtual biotech firms benefit from outsourcing to access specialized capabilities without heavy internal capital outlays.

  • Recent moves illustrate the shift: Lonza expanded a U.S. partnership on two biologics programs, while Samsung Biologics' CHF 1.46 billion bid for PolyPeptide CDMO aims to broaden peptide and biologics capabilities.

Summary based on 1 source


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