CDMO market size | Forecast and Future Outlook 2025

Code: MTA4141 Publication Date: Jun 2025

What is the CDMO Market Size?

According to 6Wresearch internal database and industry insights, the Global Contract Development and Manufacturing Organization (CDMO) market was estimated at approximately USD 145 billion in 2024 and is expected to surpass USD 289 billion by 2031, exhibiting a CAGR of 10.1%.

This growth is driven by rising outsourcing in the pharmaceutical sector, increased demand for biologics, and the need for cost-effective drug development and manufacturing.

Key Growth Drivers

  • Surge in demand for large and small molecule drug development.
  • Expansion of biologics and advanced therapy medicinal products (ATMPs).
  • Cost efficiency and scalability offered by CDMO partnerships.
  • Growing number of virtual and small biotech firms lacking in-house capabilities.
  • Accelerated timelines for clinical trials and drug commercialization.
  • Increasing regulatory compliance requirements prompting external support.

CDMO Market Trends 

CDMO Market is expected to evolve with trends such as greater integration of digital manufacturing platforms, AI-powered process optimization, and expansion in biologics-focused facilities. The increased need of fill-finish solutions, personalized healthcare, and modular manufacturing units is transforming the way the operations happen. Moreover, the CDMOs are stepping up in terms of the global GMP-compliant infrastructure to respond to the increased expectations of global regulatory authorities as well as pharmaceutical innovators. CDMOs and biotech firm strategic partnerships are also up and contribute to pipeline support. Further, there is a rise in promoting sustainability and energy-saving production throughout CDMO activity.

Major Companies

  • Lonza Group
  • Catalent Inc.
  • Thermo Fisher Scientific
  • Samsung Biologics
  • WuXi AppTec
  • Boehringer Ingelheim BioXcellence
CDMO market size : FAQs
Biologics and small molecule APIs are the leading segments due to increasing demand for high-quality, outsourced pharmaceutical services.
Capacity constraints, technology transfer complexities, and maintaining regulatory compliance across geographies remain core challenges.
The rise of virtual biotech companies and need for flexible, scalable solutions are prompting more pharma firms to engage CDMO partnerships.
Digital twins, single-use technologies, and continuous manufacturing systems are modernizing the CDMO landscape for better efficiency and compliance.
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