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The South Korea CDMO market was valued at USD 6.11 Billion in 2025 and is expected to grow at a CAGR of 5.20%, reaching USD 10.14 Billion by 2035. The market growth is driven by robust domestic infrastructure and government prioritization of biopharma as a national growth engine across the region. In addition, strategic public-private investments, such as the Songdo Bio Campus expansion, and the government’s Third Five-Year Plan to double pharmaceutical exports by 2027 are unlocking significant opportunities.
Base Year
Historical Period
Forecast Period
Legislative flexibility is enhancing export potential of the region, boosting global competitiveness.
The market growth is driven by the rising emphasis on biologics and ADC-focused infrastructure investment is driving capacity growth and market share leadership.
Major market trends include cross-border partnerships and development of innovation clusters like Songdo, that are positioning South Korea as a global CDMO hub.
Compound Annual Growth Rate
5.2%
Value in USD Billion
2026-2035
*this image is indicative*
The South Korea CDMO market plays a vital role in scaling biopharmaceutical production, reducing time-to-market, and supporting the country's growing role as a global biologics manufacturing hub. Driven by supportive policy frameworks, private sector expansion, and strong global partnerships, South Korea’s CDMO industry is central to improving healthcare access and competitiveness across international pharmaceutical supply chains. The South Korean government has established policies that provide incentives for the growth of the biopharmaceutical industry. These include funding for research and development, favorable tax policies for foreign direct investment, and regulatory support for biopharmaceutical companies. This environment has led to the establishment of numerous CDMO facilities that cater to both local and international clients.
Implementation of National Strategies to Position Korea Among Global Biopharma Leaders
Supportive industrial policy, rising biologics demand, and a skilled R&D workforce are key market drivers. For instance, as part of its Third Five-Year Comprehensive Plan announced in 2023, South Korea aims to be one of the world’s top six pharmaceutical powerhouses by 2027. The plan emphasizes doubling biopharma exports and expanding clinical trials nationwide. This policy is likely to foster innovation, increase investment, and accelerate the CDMO sector’s market value throughout the forecast period.
Strategic Collaborations Enhancing Infrastructure and Innovation to Boost South Korea CDMO Market Demand
Increasing partnerships between local and global players are improving capabilities and operational scale. For instance, in July 2024, Lotte Biologics and Merck KGaA announced a partnership at the Songdo Bio Campus, focusing on joint lab operations and securing raw material supply chains. This collaboration is expected to strengthen South Korea’s domestic bioproduction infrastructure, attract biotech ventures, and solidify the nation’s status as a preferred outsourcing destination for biopharma manufacturing during the forecast period.
Major market trends include regulatory enhancements and facility expansions supporting industry competitiveness.
Regulatory Reforms Strengthening Export Flexibility and Global Competitiveness
Favorable government policies and deregulation are improving international market access and operational flexibility for CDMOs. For instance, in January 2025, the South Korean Ministry of Health and Welfare introduced the “Biopharmaceutical CDMO Support Act,” allowing CDMO exports without requiring a pharmaceutical manufacturing license. This reform is expected to eliminate major bottlenecks in logistics and licensing, enabling faster delivery and improving international positioning, thus bolstering market growth through enhanced export efficiency in the forecast period.
High-Value Manufacturing Expansions to Boost South Korea CDMO Market Value
Growing global demand for advanced biologics and antibody-drug conjugates (ADCs) is fueling facility expansions in South Korea. For instance, in May 2024, Lotte Biologics broke ground on a USD 3.3 billion CDMO mega-plant in Incheon’s Songdo Bio Campus, aiming to boost its biologics capacity to 360,000 liters. This major investment is set to enhance South Korea’s infrastructure competitiveness, create contract opportunities, and significantly increase its share in the global CDMO market over the coming years.
Pharmaceutical and Biopharmaceutical Companies Leading the Segment by End User
Pharmaceutical and biopharmaceutical companies are expected to hold the largest share in market by end user. It is expected a value of nearly USD 149.79 billion by 2034, owing to a growing demand for biologics, biosimilars, and precision medicines. With increased government funding and industry-focused incentives, more Korean drug developers are outsourcing complex processes to CDMOs. Additionally, the rise of domestic biopharma players like Samsung Biologics and Lotte Biologics has expanded demand for GMP-compliant, scalable manufacturing solutions. Meanwhile, medical device firms and others contribute modestly, and are expected to witness a CAGR of 10.6% during the forecast period.
The key features of the market report comprise grants analysis, funding and investment analysis, and strategic initiatives by the leading players. The major companies in the market are as follows:
Headquartered in Germany and founded in 1950, Vetter Pharma is a global CDMO specializing in aseptic filling and packaging of injectables. The company has expanded its Asia-Pacific footprint, including a clinical supply center in South Korea to support local and regional biopharma clients. Its high standards in sterility assurance, regulatory compliance, and innovation make it a critical partner for Korean pharmaceutical firms seeking high-quality parenteral manufacturing and packaging solutions.
Founded in 1995 and headquartered in Sweden, Recipharm is a leading CDMO offering development and manufacturing services across biologics, sterile injectables, and oral solids. In 2024, the company announced plans to expand its footprint in Asia through commercial partnerships, including collaborations in South Korea’s biosimilars and mRNA space. Recipharm’s emphasis on flexible, scalable manufacturing platforms and strong regulatory alignment positions it as a strategic outsourcing partner for Korean drug developers.
Established in 1885 and based in Germany, Boehringer Ingelheim operates globally with strong biologics CDMO services through its BioXcellence™ brand. Its collaboration with Korean biopharma firms and strong interest in Asia-Pacific biologics development have increased its local relevance. Boehringer is known for mammalian cell culture expertise and clinical-to-commercial scale capabilities, making it an attractive CDMO partner for South Korea’s rapidly evolving biologics market and biosimilar production landscape.
A division of Thermo Fisher Scientific, Patheon provides end-to-end CDMO services for small and large molecules. While headquartered in the United States, Patheon has increased its involvement in South Korea by supporting clinical supply chains and offering global regulatory support for Korean biopharma exports. With investments in biologics manufacturing and integrated solutions, Patheon enables Korean clients to streamline product development and accelerate global market entry through scalable CDMO solutions.
*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 Pfizer Inc., Samsung Biologics Co., Ltd., Lonza Group, CELLTRION INC., WuXi AppTec, 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
*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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| Market Dynamics |
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| Supplier Landscape |
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| Companies Covered |
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