South Korea BioPharma Contract Research & CDMO Market

South Korea BioPharma Contract Research & CDMO Market, valued at USD 5 Bn, grows with rising biopharma needs, tech advancements, and regulatory support for innovation.

Region:Asia

Author(s):Shubham

Product Code:KRAB3231

Pages:96

Published On:October 2025

About the Report

Base Year 2024

South Korea BioPharma Contract Research & CDMO Market Overview

  • The South Korea BioPharma Contract Research & CDMO Market is valued at USD 5 billion, based on a five-year historical analysis. This growth is primarily driven by the increasing demand for biopharmaceuticals, advancements in drug development technologies, and a robust regulatory framework that supports innovation in the sector.
  • Key players in this market include Seoul, Incheon, and Busan, which dominate due to their strategic locations, advanced infrastructure, and concentration of research institutions and biopharma companies. These cities provide a conducive environment for collaboration and innovation, further enhancing the market's growth potential.
  • In 2023, the South Korean government implemented the "Biohealth Industry Promotion Act," aimed at fostering the growth of the biopharmaceutical sector. This regulation includes incentives for research and development, streamlined approval processes for new drugs, and support for international collaborations, thereby enhancing the competitiveness of the domestic bio-pharma industry.
South Korea BioPharma Contract Research & CDMO Market Size

South Korea BioPharma Contract Research & CDMO Market Segmentation

By Type:The market is segmented into various types, including Contract Research Organizations (CROs), Contract Development and Manufacturing Organizations (CDMOs), Analytical Testing Services, Biologics Manufacturing, Small Molecule Manufacturing, and Others. Among these, Contract Research Organizations (CROs) are leading the market due to their essential role in providing outsourced research services to pharmaceutical and biotechnology companies. The increasing complexity of clinical trials and the need for specialized expertise have driven demand for CROs, making them a critical component of the biopharma ecosystem.

South Korea BioPharma Contract Research & CDMO Market segmentation by Type.

By End-User:The end-user segmentation includes Pharmaceutical Companies, Biotechnology Firms, Academic Institutions, Government Research Organizations, and Others. Pharmaceutical Companies are the dominant end-users, driven by their need for efficient drug development processes and the increasing complexity of regulatory requirements. The collaboration between pharmaceutical companies and CROs has become essential for accelerating drug development timelines and ensuring compliance with regulatory standards.

South Korea BioPharma Contract Research & CDMO Market segmentation by End-User.

South Korea BioPharma Contract Research & CDMO Market Competitive Landscape

The South Korea BioPharma Contract Research & CDMO Market is characterized by a dynamic mix of regional and international players. Leading participants such as Samsung Biologics, SK Biopharmaceuticals, Celltrion, Hanmi Pharmaceutical, LG Chem, Daewoong Pharmaceutical, CJ Healthcare, Medytox, Genexine, Green Cross Corporation, PharmAbcine, ST Pharm, Yuhan Corporation, Dong-A ST, Ildong Pharmaceutical contribute to innovation, geographic expansion, and service delivery in this space.

Samsung Biologics

2011

Incheon, South Korea

SK Biopharmaceuticals

2017

Seongnam, South Korea

Celltrion

2002

Incheon, South Korea

Hanmi Pharmaceutical

1973

Seoul, South Korea

LG Chem

1947

Seoul, South Korea

Company

Establishment Year

Headquarters

Group Size (Large, Medium, or Small as per industry convention)

Revenue Growth Rate

Client Retention Rate

Project Turnaround Time

Market Penetration Rate

Pricing Strategy

South Korea BioPharma Contract Research & CDMO Market Industry Analysis

Growth Drivers

  • Increasing Demand for Biopharmaceuticals:The South Korean biopharmaceutical market is projected to reach approximately $5.5 billion in future, driven by a growing prevalence of chronic diseases. The World Health Organization reported that 1 in 4 South Koreans suffers from chronic conditions, increasing the need for innovative therapies. This demand is further supported by the country's aging population, with over 17% aged 65 and older, necessitating advanced biopharmaceutical solutions to improve health outcomes.
  • Rise in Outsourcing of R&D Activities:In future, it is estimated that around 60% of South Korean biopharma companies will outsource their R&D activities to contract research organizations (CROs) and contract development and manufacturing organizations (CDMOs). This trend is fueled by the need to reduce operational costs, enhance efficiency, and access specialized expertise. The South Korean government has also initiated programs to support outsourcing, further driving this growth in the sector.
  • Government Support for Biotech Innovation:The South Korean government allocated approximately $1.2 billion in future to support biotech innovation and research initiatives. This funding aims to foster collaboration between public and private sectors, enhancing the development of biopharmaceuticals. Additionally, the government has implemented tax incentives and grants for biotech firms, encouraging investment in research and development, which is crucial for the growth of the bioPharma contract research and CDMO market.

Market Challenges

  • Stringent Regulatory Requirements:The South Korean bioPharma sector faces rigorous regulatory frameworks, which can delay the approval of new drugs and therapies. The Ministry of Food and Drug Safety (MFDS) has stringent guidelines that require extensive clinical trials and documentation, often extending timelines by 12-18 months. This regulatory environment can deter smaller firms from entering the market, limiting innovation and competition within the industry.
  • High Competition Among Service Providers:The South Korean bioPharma contract research and CDMO market is characterized by intense competition, with over 200 registered CROs and CDMOs. This saturation leads to price wars and reduced profit margins, making it challenging for new entrants to establish themselves. Established players dominate the market, often leveraging economies of scale, which can stifle innovation and limit opportunities for smaller firms to thrive.

South Korea BioPharma Contract Research & CDMO Market Future Outlook

The South Korean bioPharma contract research and CDMO market is poised for significant transformation, driven by advancements in personalized medicine and digital technologies. As the industry shifts towards patient-centric approaches, companies are increasingly adopting innovative methodologies to enhance clinical trial efficiency. Furthermore, collaborations with academic institutions are expected to foster research breakthroughs, enabling the development of novel therapies. This dynamic environment will likely attract more investments, positioning South Korea as a leading hub for biopharmaceutical innovation in the Asia-Pacific region.

Market Opportunities

  • Growth in Personalized Medicine:The personalized medicine market in South Korea is projected to reach $1.8 billion in future, driven by advancements in genomics and biotechnology. This growth presents opportunities for CDMOs to develop tailored therapies, enhancing treatment efficacy and patient outcomes. Companies that invest in personalized medicine capabilities can gain a competitive edge in this rapidly evolving landscape.
  • Expansion into Emerging Markets:South Korean bioPharma companies are increasingly looking to expand into emerging markets, particularly in Southeast Asia, where demand for biopharmaceuticals is rising. The region's growing healthcare expenditure, projected to reach $200 billion in future, offers lucrative opportunities for South Korean firms to establish partnerships and expand their market presence, driving growth in the contract research and CDMO sectors.

Scope of the Report

SegmentSub-Segments
By Type

Contract Research Organizations (CROs)

Contract Development and Manufacturing Organizations (CDMOs)

Analytical Testing Services

Biologics Manufacturing

Small Molecule Manufacturing

Others

By End-User

Pharmaceutical Companies

Biotechnology Firms

Academic Institutions

Government Research Organizations

Others

By Service Type

Preclinical Services

Clinical Development Services

Commercial Manufacturing Services

Regulatory Affairs Services

Others

By Therapeutic Area

Oncology

Cardiovascular

Neurology

Infectious Diseases

Others

By Region

Seoul

Busan

Incheon

Daegu

Others

By Client Type

Large Enterprises

Small and Medium Enterprises (SMEs)

Startups

Others

By Pricing Model

Fixed Pricing

Cost-Plus Pricing

Performance-Based Pricing

Others

Key Target Audience

Investors and Venture Capitalist Firms

Government and Regulatory Bodies (e.g., Ministry of Food and Drug Safety, Korea Health Industry Development Institute)

Pharmaceutical and Biotechnology Companies

Contract Research Organizations (CROs)

Contract Development and Manufacturing Organizations (CDMOs)

Healthcare Providers and Hospitals

Biopharmaceutical Supply Chain Partners

Pharmaceutical Industry Associations

Players Mentioned in the Report:

Samsung Biologics

SK Biopharmaceuticals

Celltrion

Hanmi Pharmaceutical

LG Chem

Daewoong Pharmaceutical

CJ Healthcare

Medytox

Genexine

Green Cross Corporation

PharmAbcine

ST Pharm

Yuhan Corporation

Dong-A ST

Ildong Pharmaceutical

Table of Contents

Market Assessment Phase

1. Executive Summary and Approach


2. South Korea BioPharma Contract Research & CDMO Market Overview

2.1 Key Insights and Strategic Recommendations

2.2 South Korea BioPharma Contract Research & CDMO Market Overview

2.3 Definition and Scope

2.4 Evolution of Market Ecosystem

2.5 Timeline of Key Regulatory Milestones

2.6 Value Chain & Stakeholder Mapping

2.7 Business Cycle Analysis

2.8 Policy & Incentive Landscape


3. South Korea BioPharma Contract Research & CDMO Market Analysis

3.1 Growth Drivers

3.1.1 Increasing demand for biopharmaceuticals
3.1.2 Rise in outsourcing of R&D activities
3.1.3 Government support for biotech innovation
3.1.4 Expansion of clinical trial activities

3.2 Market Challenges

3.2.1 Stringent regulatory requirements
3.2.2 High competition among service providers
3.2.3 Limited access to funding for startups
3.2.4 Variability in quality standards

3.3 Market Opportunities

3.3.1 Growth in personalized medicine
3.3.2 Expansion into emerging markets
3.3.3 Technological advancements in drug development
3.3.4 Collaborations with academic institutions

3.4 Market Trends

3.4.1 Increased focus on biologics
3.4.2 Adoption of digital technologies in research
3.4.3 Shift towards patient-centric trials
3.4.4 Growth of integrated service providers

3.5 Government Regulation

3.5.1 New drug approval processes
3.5.2 Clinical trial regulations
3.5.3 Quality assurance standards
3.5.4 Intellectual property protections

4. SWOT Analysis


5. Stakeholder Analysis


6. Porter's Five Forces Analysis


7. South Korea BioPharma Contract Research & CDMO Market Market Size, 2019-2024

7.1 By Value

7.2 By Volume

7.3 By Average Selling Price


8. South Korea BioPharma Contract Research & CDMO Market Segmentation

8.1 By Type

8.1.1 Contract Research Organizations (CROs)
8.1.2 Contract Development and Manufacturing Organizations (CDMOs)
8.1.3 Analytical Testing Services
8.1.4 Biologics Manufacturing
8.1.5 Small Molecule Manufacturing
8.1.6 Others

8.2 By End-User

8.2.1 Pharmaceutical Companies
8.2.2 Biotechnology Firms
8.2.3 Academic Institutions
8.2.4 Government Research Organizations
8.2.5 Others

8.3 By Service Type

8.3.1 Preclinical Services
8.3.2 Clinical Development Services
8.3.3 Commercial Manufacturing Services
8.3.4 Regulatory Affairs Services
8.3.5 Others

8.4 By Therapeutic Area

8.4.1 Oncology
8.4.2 Cardiovascular
8.4.3 Neurology
8.4.4 Infectious Diseases
8.4.5 Others

8.5 By Region

8.5.1 Seoul
8.5.2 Busan
8.5.3 Incheon
8.5.4 Daegu
8.5.5 Others

8.6 By Client Type

8.6.1 Large Enterprises
8.6.2 Small and Medium Enterprises (SMEs)
8.6.3 Startups
8.6.4 Others

8.7 By Pricing Model

8.7.1 Fixed Pricing
8.7.2 Cost-Plus Pricing
8.7.3 Performance-Based Pricing
8.7.4 Others

9. South Korea BioPharma Contract Research & CDMO Market Competitive Analysis

9.1 Market Share of Key Players

9.2 Cross Comparison of Key Players

9.2.1 Company Name
9.2.2 Group Size (Large, Medium, or Small as per industry convention)
9.2.3 Revenue Growth Rate
9.2.4 Client Retention Rate
9.2.5 Project Turnaround Time
9.2.6 Market Penetration Rate
9.2.7 Pricing Strategy
9.2.8 Service Diversification Index
9.2.9 Customer Satisfaction Score
9.2.10 Innovation Index

9.3 SWOT Analysis of Top Players

9.4 Pricing Analysis

9.5 Detailed Profile of Major Companies

9.5.1 Samsung Biologics
9.5.2 SK Biopharmaceuticals
9.5.3 Celltrion
9.5.4 Hanmi Pharmaceutical
9.5.5 LG Chem
9.5.6 Daewoong Pharmaceutical
9.5.7 CJ Healthcare
9.5.8 Medytox
9.5.9 Genexine
9.5.10 Green Cross Corporation
9.5.11 PharmAbcine
9.5.12 ST Pharm
9.5.13 Yuhan Corporation
9.5.14 Dong-A ST
9.5.15 Ildong Pharmaceutical

10. South Korea BioPharma Contract Research & CDMO Market End-User Analysis

10.1 Procurement Behavior of Key Ministries

10.1.1 Ministry of Health and Welfare
10.1.2 Ministry of Food and Drug Safety
10.1.3 Ministry of Science and ICT

10.2 Corporate Spend on Infrastructure & Energy

10.2.1 Investment in R&D Facilities
10.2.2 Budget Allocation for Clinical Trials
10.2.3 Spending on Regulatory Compliance

10.3 Pain Point Analysis by End-User Category

10.3.1 Biopharma Companies
10.3.2 Research Institutions
10.3.3 Government Agencies

10.4 User Readiness for Adoption

10.4.1 Awareness of New Technologies
10.4.2 Training and Skill Development
10.4.3 Infrastructure Readiness

10.5 Post-Deployment ROI and Use Case Expansion

10.5.1 Measurement of ROI
10.5.2 Case Studies of Successful Implementations
10.5.3 Future Use Case Opportunities

11. South Korea BioPharma Contract Research & CDMO Market Future Size, 2025-2030

11.1 By Value

11.2 By Volume

11.3 By Average Selling Price


Go-To-Market Strategy Phase

1. Whitespace Analysis + Business Model Canvas

1.1 Market Gaps Identification

1.2 Business Model Framework


2. Marketing and Positioning Recommendations

2.1 Branding Strategies

2.2 Product USPs


3. Distribution Plan

3.1 Urban Retail Strategies

3.2 Rural NGO Tie-Ups


4. Channel & Pricing Gaps

4.1 Underserved Routes

4.2 Pricing Bands


5. Unmet Demand & Latent Needs

5.1 Category Gaps

5.2 Consumer Segments


6. Customer Relationship

6.1 Loyalty Programs

6.2 After-Sales Service


7. Value Proposition

7.1 Sustainability

7.2 Integrated Supply Chains


8. Key Activities

8.1 Regulatory Compliance

8.2 Branding

8.3 Distribution Setup


9. Entry Strategy Evaluation

9.1 Domestic Market Entry Strategy

9.1.1 Product Mix
9.1.2 Pricing Band
9.1.3 Packaging

9.2 Export Entry Strategy

9.2.1 Target Countries
9.2.2 Compliance Roadmap

10. Entry Mode Assessment

10.1 Joint Ventures

10.2 Greenfield Investments

10.3 Mergers & Acquisitions

10.4 Distributor Model


11. Capital and Timeline Estimation

11.1 Capital Requirements

11.2 Timelines


12. Control vs Risk Trade-Off

12.1 Ownership vs Partnerships


13. Profitability Outlook

13.1 Breakeven Analysis

13.2 Long-Term Sustainability


14. Potential Partner List

14.1 Distributors

14.2 Joint Ventures

14.3 Acquisition Targets


15. Execution Roadmap

15.1 Phased Plan for Market Entry

15.1.1 Market Setup
15.1.2 Market Entry
15.1.3 Growth Acceleration
15.1.4 Scale & Stabilize

15.2 Key Activities and Milestones

15.2.1 Milestone Planning
15.2.2 Activity Tracking

Research Methodology

ApproachModellingSample

Phase 1: Approach1

Desk Research

  • Analysis of industry reports from South Korean bio-pharma associations and government publications
  • Review of market trends and forecasts from academic journals and research papers
  • Examination of regulatory frameworks and compliance guidelines from the Ministry of Food and Drug Safety (MFDS)

Primary Research

  • Interviews with executives from leading Contract Research Organizations (CROs) and Contract Development and Manufacturing Organizations (CDMOs)
  • Surveys targeting R&D managers and project leads in bio-pharma companies
  • Field interviews with regulatory affairs specialists to understand compliance challenges

Validation & Triangulation

  • Cross-validation of findings through multiple data sources including trade publications and market surveys
  • Triangulation of qualitative insights from interviews with quantitative data from market reports
  • Sanity checks conducted through expert panel reviews comprising industry veterans

Phase 2: Market Size Estimation1

Top-down Assessment

  • Estimation of the bio-pharma market size based on national healthcare expenditure and R&D investment trends
  • Segmentation of the market by therapeutic areas and service types offered by CROs and CDMOs
  • Incorporation of government initiatives promoting bio-pharma innovation and funding

Bottom-up Modeling

  • Collection of revenue data from key players in the bio-pharma contract research and manufacturing space
  • Operational cost analysis based on service pricing models and project scopes
  • Volume estimates derived from historical project data and client contracts

Forecasting & Scenario Analysis

  • Multi-factor regression analysis incorporating variables such as technological advancements and market demand shifts
  • Scenario modeling based on potential changes in regulatory landscapes and global market dynamics
  • Development of baseline, optimistic, and pessimistic forecasts through 2030

Phase 3: CATI Sample Composition1

Scope Item/SegmentSample SizeTarget Respondent Profiles
Contract Research Organizations100Business Development Managers, Project Managers
Contract Manufacturing Organizations80Operations Directors, Quality Assurance Managers
Biotech Startups60Founders, R&D Leads
Pharmaceutical Companies90Clinical Research Coordinators, Regulatory Affairs Managers
Academic Research Institutions70Principal Investigators, Lab Managers

Frequently Asked Questions

What is the current value of the South Korea BioPharma Contract Research & CDMO Market?

The South Korea BioPharma Contract Research & CDMO Market is valued at approximately USD 5 billion, driven by the increasing demand for biopharmaceuticals and advancements in drug development technologies.

What are the key drivers of growth in the South Korea BioPharma market?

Which cities are the main hubs for the BioPharma Contract Research & CDMO Market in South Korea?

What is the impact of the "Biohealth Industry Promotion Act" on the market?

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