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The Asia Pacific CDMO market was valued at USD 64.78 Billion in 2025, driven by rising pharmaceutical outsourcing and the growing demand for active pharmaceutical ingredients (APIs) across the region. The market is projected to grow at a CAGR of 11.60% during the forecast period of 2026–2035, potentially reaching a value of USD 194.13 Billion by 2035.
Base Year
Historical Period
Forecast Period
The rising prevalence of asthma, affecting approximately 46 million adults in China alone, is significantly contributing to increased demand for respiratory drug development and manufacturing, thereby driving growth in the Asia Pacific CDMO market.
In September 2023, WuXi Vaccines launched its first standalone vaccine CDMO site in Suzhou, China. This expansion of end-to-end vaccine services is expected to accelerate project timelines and drive Asia Pacific CDMO market growth.
The rising demand for cost-effective, scalable manufacturing solutions, driving growth in the Asia Pacific CDMO market. Key players are expanding capabilities and facilities to meet growing biopharmaceutical outsourcing needs across the region.
Compound Annual Growth Rate
11.6%
Value in USD Billion
2026-2035
*this image is indicative*
Contract Development and Manufacturing Organizations (CDMOs) offer end-to-end solutions to pharmaceutical and biotechnology companies, encompassing drug development, manufacturing, and related services. These organizations enable firms to accelerate product timelines, optimize costs, and access specialized expertise without expanding internal infrastructure. The CDMO market in Asia Pacific is experiencing robust growth, driven by strong regional manufacturing capabilities, favorable regulatory environments, and increasing demand for cost-effective drug development. Rising investments in biologics and personalized medicine further support market expansion. The market was valued at USD 64.78 Billion in 2025, with growth fueled by strategic collaborations, rising exports, and increasing pharmaceutical outsourcing across the region.
One of the key drivers of this growth is the increasing incidence of chronic and preventable diseases across Asia Pacific, prompting pharmaceutical companies to outsource drug development and manufacturing to specialized CDMOs. For example, the rising burden of cervical cancer in the region has become a significant concern. According to Roche, over half of global cervical cancer deaths occur in Asia-Pacific, with projections indicating a further rise in the coming decade. This growing health challenge underscores the urgent need for efficient therapeutic development, thereby amplifying the role of CDMOs in ensuring faster, scalable, and cost-effective production, ultimately driving market expansion.
Another major growth driver is the ongoing expansion in API manufacturing capacity across the region. To meet increasing global demand for high-quality and high-potency APIs, several CDMOs are investing in technologically advanced infrastructure. Notably, in February 2023, Piramal Pharma Solutions announced the launch of initial production batches at its newly expanded API facility in Riverview, Michigan. The facility, part of the USD 38 million Project PRIME Phase 1, significantly enhanced the company’s capability to produce high-potency APIs and scale clinical trial materials. This development reflects a broader regional push to expand manufacturing capabilities, reinforcing the strategic importance of CDMOs and propelling market growth.
The market is experiencing several emerging trends, notably the rise of strategic collaborations in cell and gene therapy CDMO services.
Strategic Collaborations in Cell and Gene Therapy CDMO Expected to Boost Asia Pacific Market Value
The formation of strategic partnerships aimed at enhancing cell and gene therapy capabilities is a notable trend in the market. For instance, in October 2024, Teijin Limited and Singapore-based Hilleman Laboratories signed a Memorandum of Understanding to expand CDMO services across the region. This partnership focuses on supporting Japanese clients entering Asia-Pacific and attracting overseas clients to Japan. Such initiatives are likely to significantly boost market growth in the Asia Pacific region.
Contract Manufacturing Organizations Expected to Dominate the Market
The Asia Pacific CDMO market is segmented by service type into contract manufacturing organizations (CMOs) and contract research organizations (CROs). While both segments play vital roles, the CMO segment is expected to lead the market due to its robust growth trajectory. According to the EMR report, the CMO segment reached USD 41.39 billion in 2024 and is projected to grow significantly, reaching USD 122.42 billion by 2034 at a CAGR of 11.8%. This growth is fueled by increasing demand for advanced therapeutic solutions and the rising outsourcing of manufacturing activities by pharmaceutical companies.
The CDMO market in Asia Pacific includes prominent regions such as China, India, Japan, ASEAN, Australia, and others. Among these, China is expected to hold a significant share in the market, supported by its advanced manufacturing capabilities, cost-effective operations, favorable government policies, and rapid growth in the biologics and pharmaceutical sectors. According to EMR report, China’s CDMO segment is projected to increase from USD 22.98 billion in 2025 to USD 62.02 billion by 2034, registering a robust CAGR of 11.7%.
The Asia Pacific CDMO market research report by Expert Market Research provides an in-depth analysis of the competitive landscape, offering key insights into funding trends, investments, and strategic initiatives by major players. Additionally, the report details strategic activities by leading companies, including regional expansions, adoption of new technologies, and efforts to enhance capacity, helping stakeholders better understand the market dynamics and positions of key industry players. Some of the leading players are as follows:
Vetter Pharma stands as a premier contract development and manufacturing organization (CDMO) with a global footprint, delivering specialized aseptic fill-and-finish services. Its expertise spans the entire product lifecycle, from early-phase development through to large-scale commercial production. Notably active in the Asia Pacific region, Vetter provides advanced support in injectable manufacturing, device integration, quality control, and compliance with international regulatory standards.
Recipharm is a global CDMO offering a wide array of manufacturing and development services across oral, sterile, and biologic drug formats. In October 2024, the company formed a strategic partnership with Exela Pharma Sciences, enabling annual output exceeding 100 million units of vials and pre-filled syringes, including vaccines and high-value biologics like GLP-1s and ADCs. It also introduced a new modular Grade A aseptic line in Germany to further support early-stage to clinical-scale projects.
Operating under Thermo Fisher Scientific, Patheon delivers end-to-end CDMO solutions for pharmaceutical and biotech companies across the Asia Pacific. Their offerings cover everything from API development to advanced biologics manufacturing, including viral vectors and cGMP-grade plasmids. Patheon’s fill-finish services cater to a variety of delivery formats such as vials, ampoules, and pre-filled syringes, with flexible capabilities that support clients at every stage from development to market launch.
Pfizer Inc. contributes to the CDMO landscape through its dedicated division, Pfizer CentreOne, which supports partners with integrated contract manufacturing solutions. Utilizing Pfizer’s global network, the division offers end-to-end services for sterile injectables, oral solid dosages, biologics, and APIs. Pfizer CentreOne’s presence in the Asia Pacific strengthens its capacity to deliver high-quality products efficiently, underpinned by regulatory expertise and lifecycle management tailored to evolving industry needs.
*Please note that this is only a partial list; the complete list of key players is available in the full report. Additionally, the list of key players can be customized to better suit your needs.*
Other key players in the market include Boehringer Ingelheim, Famar SA, Lonza Group, Novotech Pty Ltd., WuXi AppTec, Fareva SA, FUJIFILM Diosynth Biotechnologies, Nipro Pharma Corporation, B. Braun SE, and WuXi Biologics.
The market report offers a detailed analysis of the market based on the following segments:
Market Breakup by Service Type
Market Breakup by Therapeutic Area
Market Breakup by End User
Market Breakup by Country
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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| REPORT FEATURES | DETAILS |
| Base Year | 2025 |
| Historical Period | 2019-2025 |
| Forecast Period | 2026-2035 |
| Scope of the Report |
Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:
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| Breakup by Service Type |
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| Breakup by Therapeutic Area |
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| Breakup by End User |
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| Breakup by Region |
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| Market Dynamics |
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| Supplier Landscape |
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| Companies Covered |
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