Globenewswire·2026-02-03 09:01Market Overview - The Pharmaceutical Contract Development and Manufacturing Organization (CDMO) market is projected to grow from USD 258.88 billion in 2025 to USD 275.27 billion in 2026, reaching USD 374.68 billion by 2031, with a CAGR of 6.33% from 2026 to 2031 [2]. Market Drivers - There is a robust outsourcing demand for complex biologics, high-potency APIs (HPAPIs), and AI-enabled process-development platforms, which are driving market growth [3]. - Increasing outsourcing volume by large pharmaceutical companies is influenced by escalating R&D costs and pipeline complexity, leading to a preference for asset-light models that leverage CDMO expertise [5]. - The surge in biologics and complex-molecule pipelines is evident, with biological entities dominating new-drug filings, including antibody-drug conjugates and mRNA vaccines [6]. Geographic Insights - North America held a 37.95% revenue share in 2025, supported by premier biologics programs and a deep venture-capital pool [9]. - The Asia-Pacific region is expected to grow at the fastest rate of 7.18% CAGR through 2031, with significant investments in mega-plants for mAbs and oligonucleotides [10]. - Europe is experiencing steady expansion, with Germany and the UK leading in quality and innovation despite Brexit challenges [11]. Market Trends - Consolidation in the industry is evident, as seen in Novo Holdings' USD 16.5 billion acquisition of Catalent, indicating a shift towards end-to-end CDMO providers [4]. - The demand for specialist partners is amplified by the need for compliance with stringent multi-region regulatory requirements, which challenge smaller entrants [8]. Competitive Landscape - Major players in the market include Thermo Fisher Scientific, Lonza Group, Catalent, and Samsung Biologics, among others, with strategic moves and market share analysis highlighting their competitive positioning [17].