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Global CDMO market Segmentation By Service (API/bulk drugs, Drug product manufacturing, Packaging), By Product (Small molecules, Biologics), By Region (North America, LATAM, APAC, EMEA)

CDMO Market Overview:

The global CDMO Market size will be growing at a CAGR of 12.76% from 2024 to 2030. This growth is attributed to Increasing Demand for Biologics and Biosimilars. The growing demand for biologics, biosimilars, and other complex molecules necessitates specialized manufacturing capabilities, boosting the demand for CDMOs with expertise in this field.CDMO stands for Contract Development and Manufacturing Organization. The CDMO market refers to a sector within the pharmaceutical and biotechnology industry where companies offer services to assist other companies in the development, manufacturing, and sometimes commercialization of drug products. In the CDMO market, organizations provide a range of services, including drug formulation, process development, analytical testing, clinical trial materials manufacturing, and commercial-scale manufacturing of pharmaceuticals. These services are typically offered on a contract basis, allowing pharmaceutical and biotech companies to outsource certain aspects of drug development and manufacturing, enabling them to focus on their core competencies and bring their products to marketmore efficiently.The CDMO market is significant due to the growing complexity and cost of drug development, which has led many pharmaceutical and biotech companies to seek external expertise and capacity to accelerate the development and production of their drug candidates. The market includes a variety of players, from large global CDMOs to smaller, specialized service providers, each catering to specific needs within thedrug development and manufacturing lifecycle.

CDMO Market size
Global CDMO Market Size from year 2023-2024

CDMO Market trends:

Increasing Outsourcing of Drug Development and Manufacturing: Pharmaceutical and biotechnology companies continue to outsource a larger portion of their drug development and manufacturing activities to CDMOs. This trend is driven by the need to reduce costs, access specialized expertise, and accelerate the drug development process.

Biologics and Advanced Therapies Dominance: The demand for CDMOs specializing in biologics, cell and gene therapies, and other advanced therapies has been growing. These therapies require specialized manufacturing capabilities and expertise, making CDMOs that can handle these types of products highly sought after.

Technological Advancements and Industry 4.0 Integration: Incorporation of Industry 4.0 technologies, such as IoT (Internet of Things), AI (Artificial Intelligence), and automation, is gaining traction in CDMO operations. These technologies enhance efficiency, data analytics, process optimization, and real-time monitoring.

Collaborations and Partnerships: Collaborations between pharmaceutical companies and CDMOs are increasing, often forming strategic partnerships to optimize drug development, manufacturing processes, and supply chain efficiency. These partnerships facilitate shared risk and resource optimization.

Resilience and Supply Chain Diversification: The COVID-19 pandemic highlighted the need for supply chain resilience and diversification. Pharmaceutical companies are seeking CDMOs with diversified global manufacturing networks to mitigate risks associated with disruptions in the supply chain.

Personalized Medicine and Patient-Centric Approaches: The rise of personalized medicine has led to a demand for customized drug development and manufacturing. CDMOs are adapting to this trend by offering tailored solutions that cater to individual patient needs and treatment modalities.

CDMO Market Drivers:

Outsourcing Trends: The outsourcing of drug development and manufacturing continues to be a significant driver. Pharmaceutical and biotech companies outsource to CDMOs to access specialized expertise, reduce costs, and accelerate the drug development process.

Complexity of Drug Development: The increasing complexity of drug development, especially in areas like biologics, advanced therapies, and personalized medicine, is driving companies to seek the expertise of CDMOs that specialize in these complex areas.

Cost Efficiency and Flexibility: CDMOs offer cost-effective solutions and flexibility in manufacturing, allowing companies to scale their production without investing heavily in infrastructure. This cost-efficiency is a significant driver for smaller or emerging pharmaceutical companies.

Focus on Core Competencies: Pharmaceutical and biotech companies often choose to outsource non-core activities, such as manufacturing, to CDMOs. This allows them to concentrate on their core strengths, such as research, marketing, and sales.

Increasing Demand for Biologics and Biosimilars: The growing demand for biologics, biosimilars, and other complex molecules necessitates specialized manufacturing capabilities, boosting the demand for CDMOs with expertise in this feild.

Global Expansion and Emerging Markets: CDMOs are expanding their global footprint to access emerging markets with cost advantages and growing pharmaceutical industries. This global expansion helps in serving a broader client base and diversifying risk.

Global CDMO Market Report Scope






CAGR of 12.76%


237.6 Billion USD


Value in US Dollars and Volume in Metric Tons


by service, by product and by region


North America, APAC, LATAM, EMEA


Pierre Fabre Group, Zymo Cosmetics, Fareva, Biofarma Srl C.F, Chemineau, C.O.C., Farmaceutici Srl, Paragon Nordic Cosmetic Solutions, Kolma, Lonza, Cho Chuang Industrial Co Ltd, Vive Cosmetics

Developments in CDMO Market:

January 2019, Cambrex Corporation, a leading manufacturer of small molecule API & finished dosage forms announced the completion of its acquisition of Avista Pharma Solutions. The strategic acquisition offers a huge opportunity to Cambrex Corporation to strengthen its service offerings in small molecule CDMO

February 2022, a China-based CDMO Asymchem Inc. plans to buy Snapdragon Chemistry, a US-based company focused on continuous manufacturing and early-stage chemical process development services for the total value of USD 57.94 million. This transaction is aimed at the expansion of the business of the Chinese CDMO in the US.

February 2022, MilliporeSigma, the U.S. and Canada Life Science business sector of Merck KGaA closed the transaction marking the acquisition of Exelead for approximately USD 780 million in cash. This is expected to add to the capabilities of the LifeSciences business in becoming one the prominent CDMOs in the mRNA value chain.

Insights on the Global CDMO Markets:

The global report on the Biopharmaceuticals market is segmented by services type, by product type and by region. Biologics is the most significant segment of the Contract Development and Manufacturing Organization (CDMO) market. It plays a pivotal role in the pharmaceutical and biotechnology industries, especially in the production of biologic drugs. Biologics generates substantial revenue in the pharmaceutical and biotech industries. The market for biologics is projected to continue growing, impacting the revenue and profitability of companies operating in this segment.High-quality API manufacturing is vital for the pharmaceutical industry. It often drives the cost and availability of essential medicines, impacting drug affordability and patient access. API manufacturing plays a significant role in determining the cost of medications. Efficient and high-quality production can contribute to more affordable drugs, benefiting patients and healthcare systems.

North America, particularly the United States, holds a dominant position in the global CDMO market. It has a mature pharmaceutical industry and a high level of outsourcing, with many biopharmaceutical companies seeking CDMO services. The presence of a robust biotech industry, especially in the Boston-Cambridge area and the San Francisco Bay Area, has driven CDMO growth. These regions are hubs for innovation and development. North America is a major destination for clinical trials, leading to high demand for clinical trial material manufacturing CDMOs. The European Medicines Agency (EMA) provides a clear regulatory pathway for drug approvals, attracting pharmaceutical companies and CDMOs. Brexit has led some companies to establish additional manufacturing operations within the EU to maintain access to the single market. The Asia-Pacific region, particularly China and India, has witnessed rapid growth in the CDMO market. China is positioning itself as a global CDMO hub. China and India have implemented favourable policies to promote the biopharmaceutical and CDMO sectors. These policies include financial incentives and streamlined regulatory processes. India is a significant player in API manufacturing and is a key supplier to the global pharmaceutical market. Cross-border research collaborations with Western pharmaceutical companies are common in Asia, leading to technology transfer and knowledge exchange. Several countries in Latin America are developing local pharmaceutical production capabilities, and this has driven the demand for CDMO services.CDMO services market is expanding globally, with significant growth in North America, Europe, and the Asia-Pacific region, particularly in China and India. These regions are characterized by established pharmaceutical industries, regulatory support, and a focus on biomanufacturing and biologics.

CDMO Market Segmentation:

By Service

  • API/bulk drugs

  • Drug product manufacturing

  • Packaging

By Product:

  • Small molecules

  • Biologics

By Region:

  • North America

  • Apac


  • EMEA

CDMO Market Key Players:

  • Pierre Fabre Group

  • Zymo CosmeticsFareva,

  • Biofarma Srl

  • C.FChemineau C.O.C

  • Farmaceutici Srl

  • Paragon Nordic Cosmetic Solutions

  • Kolma

  • Lonza

  • Cho Chuang Industrial Co. Ltd.

  • Vive Cosmetics

CDMO Market Research Report

CDMO Market Report

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Key Players
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