This report provides an assessment of the 2025 global biologics contract manufacturing market, with a focus on structural capacity constraints and shifting competitive dynamics across the value chain.
The report examines how in 2025 the market was transitioning from capacity build-out to capacity access and reliability. It highlights persistent bottlenecks in critical segments and explores how sponsors and CDMOs were adapting their strategies in response. The report also analyzes ongoing key industry developments like strategic transactions, growing demand for high-volume biologics, and increasing emphasis on geographically diversified manufacturing networks.
This report provides an assessment of the 2025 global biologics contract manufacturing market, with a focus on structural capacity constraints and shifting competitive dynamics across the value chain.
The report examines how in 2025 the market was transitioning from capacity build-out to capacity access and reliability. It highlights persistent bottlenecks in critical segments and explores how sponsors and CDMOs were adapting their strategies in response. The report also analyzes ongoing key industry developments like strategic transactions, growing demand for high-volume biologics, and increasing emphasis on geographically diversified manufacturing networks.
The biologics contract development and manufacturing organization (CDMO) market has entered a markedly different phase from the post-pandemic expansion cycle. While large-scale capacity investment remained active in 2025, attention has shifted to structural constraints that persist within the value chain. These constraints are most apparent in sterile fill-finish and certain advanced therapy manufacturing processes, where validation timelines, regulatory requirements, and equipment specialization limit the pace of effective capacity expansion.
Sponsors and CDMOs increasingly focused on securing dependable access to these critical manufacturing segments, making competitive positioning centered not on how much capacity could be built, but on where that capacity was located and how reliably it could support sustained commercial demand. A notable development during this period was the acquisition of Catalent by Novo Holdings, completed in December 2024. As part of the transaction, three fill-finish facilities in Italy, Belgium, and the United States (US) were aligned with Novo Nordisk. The move highlighted the strategic importance of sterile drug-product capacity for high-volume injectable biologics and illustrated a broader tendency for sponsors to secure critical manufacturing infrastructure through ownership or long-term partnerships rather than relying solely on open CDMO capacity.
This has coincided with continued demand growth for GLP-1 and related chronic therapies, which places sustained pressure on downstream manufacturing steps such as fill-finish, device assembly, and temperature-controlled distribution. In practical terms, demand has been concentrated in parts of the value chain where capacity is harder to rapidly expand, increasing the relevance of established drug-product infrastructure.
Geographic considerations have also become more visible in manufacturing strategy. Policy discussions affecting biotechnology supply chains, alongside general supply continuity concerns, have led sponsors to make greater use of manufacturing networks spread across multiple regions. Existing facilities in North America and Europe have therefore taken on additional importance within global supply planning.
Competitive positioning is now expected to be driven less by how much new capacity is announced and more by how well existing capacity is managed, where it is located, and how reliably it can support commercial supply. For sponsors, this reinforces the need for earlier manufacturing planning and partner alignment; for CDMOs, it places greater weight on execution, targeted investment, and operational credibility.
The biologics CDMO market is increasingly segmented and across segments, companies are shifting from aggressive capacity expansion to more targeted strategies. This chapter details trends in the biologics CDMO public market landscape from the perspective of global, regional, specialized, and emerging players, and provides equity performance insights and IPO analysis.
This chapter examines how leading biotechnology companies with significant biologics portfolios performed in 2025 and explores how factors such as product mix, exposure to high-volume therapies, and pricing and competitive dynamics shaped both financial performance and equity market trends. The analysis also considers how these dynamics translate into biologics manufacturing demand.
ARTICLE – 15 MIN. READ
ARTICLE – 3 MIN. READ
The biologics CDMO market is increasingly segmented and across segments, companies are shifting from aggressive capacity expansion to more targeted strategies. This article details trends in the biologics CDMO public market landscape from the perspective of global, regional, specialized, and emerging players, and provides equity performance insights and IPO analysis.
ARTICLE – 15 MIN. READ
This article examines how leading biotechnology companies with significant biologics portfolios performed in 2025 and explores how factors such as product mix, exposure to high-volume therapies, and pricing and competitive dynamics shaped both financial performance and equity market trends. The analysis also considers how these dynamics translate into biologics manufacturing demand.
ARTICLE – 3 MIN. READ
This article explores how investments are being concentrated in core manufacturing infrastructure and adjacent capabilities, reflecting a strategic shift toward integrated, end- developments to understand how capital allocation is evolving in a more selective and maturity-driven investment environment.
ARTICLE – 6 MIN. READ
This chapter explores how investments are being concentrated in core manufacturing infrastructure and adjacent capabilities, reflecting a strategic shift toward integrated, end- developments to understand how capital allocation is evolving in a more selective and maturity-driven investment environment.
ARTICLE – 6 MIN. READ
Public market performance in 2025 indicates that biologics CDMOs have moved beyond the broad valuation compression phase that followed the post-pandemic peak and into a period of more selective repricing. Valuation levels across platforms no longer move uniformly, and differences in scale and manufacturing scope remain clearly visible in public market pricing. Forward EV/EBITDA multiples continue to range from approximately 6× to above 30×, with larger biologics manufacturers maintaining valuation levels at the upper end of the range, while smaller and more specialized platforms trade within narrower bands.
In early April 2025, the VIX reached elevated levels rarely seen outside major market stress episodes, with a spike that placed it among the largest one-week moves relative to historical patterns. This spike coincided with a period of heightened uncertainty around economic policy and trade developments, including announcements of tariff actions by major economies, which contributed to broader risk repricing in equities and other asset classes. During this period, CDMO equities declined alongside broader healthcare and equity indices. As volatility declined during the second half of the year, healthcare equities recovered, and CDMO valuations stabilized in line with broader market conditions.
Public market activity during the year also included several biologics CDMOs’ IPOs, particularly across Asia, expanding the publicly traded peer group. Post-listing performance varied across issuers. Companies with established manufacturing capacity and visible revenue base showed relatively stable trading performance, while others experienced greater share price volatility following listing. Across the broader CDMO peer group, equity performance followed a similar pattern, with larger biologics manufacturing platforms maintaining more stable valuation levels, while smaller and earlier-stage platforms recorded wider share price movements.
Evidently, capital deployment across publicly listed CDMOs remained sustained. More than $5.5 billion in disclosed investments and financings were recorded during the year, primarily directed toward biologics manufacturing expansion, including upstream capacity and fill-finish infrastructure. These investment programs continued during periods of market volatility, indicating that publicly listed CDMOs remained active in expanding manufacturing capacity.
Entering 2026, valuation levels across platforms remain differentiated, and equity performance continues to vary across the peer group. Larger, scaled biologics platforms continue to trade at structural premiums, while smaller and earlier-stage platforms remain more sensitive to execution and market volatility. The April 2025 volatility episode tested sector resilience, yet capital deployment and expansion programs continued throughout the year. As a result, 2026 begins with a sector that is no longer priced on expansion narratives alone, but increasingly on operating delivery and manufacturing scale.
We guide decisions that accelerate growth and reduce risk, from strategy and CDMO selection to commercial due diligence and execution. Discover how we help stakeholders navigate the biologics CDMO market with confidence and meet the members of our CDMO Biologics Center of Excellence.
At Alira Health, we guide decisions that accelerate growth and reduce risk, from strategy and CDMO selection to commercial due diligence and execution. Discover how we help stakeholders navigate the biologics CDMO market with confidence and meet the members of our CDMO Biologics Center of Excellence.
Subscribe to our newsletter for the latest news, events, and thought leadership