APAC biologics contract manufacturing market report Size, Share, Growth Drivers, Trends, Opportunities & Forecast 2025–2030

APAC Biologics Contract Manufacturing Market, valued at USD 11.7 Bn, grows with rising biologics demand, chronic diseases, and innovations like single-use technologies and biosimilars.

Region:Asia

Author(s):Rebecca

Product Code:KRAC4594

Pages:80

Published On:October 2025

About the Report

Base Year 2024

APAC Biologics Contract Manufacturing Market Overview

  • The APAC Biologics Contract Manufacturing Market is valued at USD 11.7 billion, based on a five-year historical analysis. This growth is primarily driven by the increasing demand for biologics, advancements in biomanufacturing technologies, and the rising prevalence of chronic diseases. The market is also supported by the growing trend of outsourcing manufacturing processes by pharmaceutical companies to reduce costs and enhance efficiency. Recent trends highlight the adoption of single-use technologies, continuous processing, and a surge in biosimilars and personalized medicine, further accelerating market expansion .
  • Key players in this market include China, Japan, and India, which dominate due to their robust pharmaceutical industries, skilled workforce, and favorable regulatory environments. China has emerged as a global hub for biologics manufacturing, leveraging significant investments in biotechnology and large-scale production capabilities. Japan and India also contribute substantially, with Japan focusing on innovation and regulatory excellence, and India strengthening its position through cost-effective manufacturing, regulatory compliance, and a growing pipeline of biosimilars. South Korea and Singapore are also notable contributors, with South Korea emphasizing cell and gene therapy manufacturing and Singapore offering a business-friendly framework and advanced infrastructure .
  • In 2023, the Indian government implemented the "National Biopharma Mission" under the Department of Biotechnology, Ministry of Science & Technology, aimed at promoting domestic production of biologics. This initiative provides incentives for research and development, streamlines regulatory processes, and supports technology transfer, collectively enhancing the country's biologics manufacturing capabilities and reducing dependency on imports. The mission sets operational standards for biopharmaceutical innovation, quality compliance, and public-private partnerships , Department of Biotechnology, Ministry of Science & Technology, Government of India, 2023.
APAC Biologics Contract Manufacturing Market Size

APAC Biologics Contract Manufacturing Market Segmentation

By Type:The market is segmented into various types, including Monoclonal Antibodies, Vaccines, Recombinant Proteins, Cell and Gene Therapies, Blood Products, Biosimilars, and Others. Among these, Monoclonal Antibodies are leading the market due to their widespread application in therapeutic areas such as oncology and autoimmune diseases. The increasing prevalence of these diseases and the growing focus on personalized medicine are driving the demand for monoclonal antibodies, making them a dominant force in the biologics contract manufacturing landscape. Single-use bioreactor technology and continuous manufacturing platforms are further supporting the rapid scale-up of monoclonal antibody production .

APAC Biologics Contract Manufacturing Market segmentation by Type.

By End-User:The end-user segmentation includes Pharmaceutical Companies, Biotechnology Firms, Academic and Research Institutions, Contract Research Organizations (CROs), and Others. Pharmaceutical Companies are the leading end-users in the market, driven by their need for efficient and cost-effective manufacturing solutions. The increasing trend of outsourcing biologics production to specialized contract manufacturers allows these companies to focus on their core competencies while ensuring high-quality product delivery. Biotechnology firms are also expanding their reliance on contract manufacturing to accelerate product development and market entry .

APAC Biologics Contract Manufacturing Market segmentation by End-User.

APAC Biologics Contract Manufacturing Market Competitive Landscape

The APAC Biologics Contract Manufacturing Market is characterized by a dynamic mix of regional and international players. Leading participants such as Samsung Biologics, WuXi Biologics, Lonza Group, Catalent, Inc., Fujifilm Diosynth Biotechnologies, Boehringer Ingelheim, AGC Biologics, Thermo Fisher Scientific, AbbVie Inc., Novartis AG, Innovent Biologics, Rentschler Biopharma, JRS Pharma, Probiogen, Toyobo Co., Ltd. contribute to innovation, geographic expansion, and service delivery in this space.

Samsung Biologics

2011

Incheon, South Korea

WuXi Biologics

2010

Wuxi, China

Lonza Group

1897

Basel, Switzerland

Catalent, Inc.

2007

Somerset, New Jersey, USA

Fujifilm Diosynth Biotechnologies

2001

Wilton, UK

Company

Establishment Year

Headquarters

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

Revenue Growth Rate (CAGR, latest fiscal year)

Market Penetration Rate (Regional/Global client base)

Customer Retention Rate (Annual renewal/contract extension rate)

Operational Efficiency (Batch success rate, lead time, capacity utilization)

Pricing Strategy (Cost leadership, premium, hybrid)

APAC Biologics Contract Manufacturing Market Industry Analysis

Growth Drivers

  • Increasing Demand for Biologics:The APAC region is witnessing a significant rise in the demand for biologics, driven by an aging population and the prevalence of chronic diseases. In future, the biopharmaceutical market in APAC is projected to reach approximately $300 billion, with biologics accounting for over 50% of this figure. This surge is attributed to the effectiveness of biologics in treating complex conditions, leading to increased investments in biologics contract manufacturing to meet this growing demand.
  • Advancements in Biomanufacturing Technologies:Technological innovations in biomanufacturing are enhancing production efficiency and reducing time-to-market for biologics. In future, the adoption of single-use technologies is expected to increase by 30%, streamlining processes and minimizing contamination risks. Additionally, the integration of automation and artificial intelligence in manufacturing processes is projected to improve yield rates by 20%, making biologics production more cost-effective and scalable in the APAC region.
  • Rising Investment in Biopharmaceutical R&D:The APAC region is experiencing a surge in investments in biopharmaceutical research and development, with funding reaching approximately $50 billion in future. This investment is driven by government initiatives and private sector funding aimed at fostering innovation in biologics. As a result, contract manufacturers are increasingly collaborating with biopharma companies to support the development of new biologics, thereby enhancing their market presence and capabilities in the region.

Market Challenges

  • Stringent Regulatory Requirements:The biologics sector in APAC faces significant challenges due to stringent regulatory frameworks. In future, compliance costs are expected to rise by 15%, impacting the profitability of contract manufacturers. Regulatory bodies are enforcing rigorous guidelines for clinical trials and product approvals, which can delay market entry and increase operational complexities. This regulatory landscape necessitates that manufacturers invest heavily in compliance and quality assurance processes to mitigate risks.
  • High Production Costs:The production costs for biologics remain a critical challenge, with estimates indicating that the average cost of manufacturing a biologic drug can exceed $1 billion. In future, rising raw material prices and labor costs are projected to increase overall production expenses by 10%. This financial burden can deter smaller contract manufacturers from entering the market, limiting competition and innovation within the APAC biologics contract manufacturing landscape.

APAC Biologics Contract Manufacturing Market Future Outlook

The future of the APAC biologics contract manufacturing market appears promising, driven by technological advancements and increasing demand for personalized medicine. As the region embraces digital transformation, manufacturers are expected to adopt innovative production techniques, enhancing efficiency and sustainability. Furthermore, the rise of biosimilars is anticipated to create new avenues for growth, allowing contract manufacturers to diversify their offerings and cater to a broader range of therapeutic areas, ultimately shaping the market landscape in the coming years.

Market Opportunities

  • Growth in Biosimilars Market:The biosimilars market in APAC is projected to grow significantly, with an estimated value of $20 billion by future. This growth presents a substantial opportunity for contract manufacturers to expand their service offerings and cater to the increasing demand for cost-effective alternatives to branded biologics, thereby enhancing their competitive edge in the market.
  • Strategic Collaborations and Partnerships:Collaborations between contract manufacturers and biopharmaceutical companies are expected to increase, with over 40% of manufacturers planning strategic partnerships in future. These alliances can facilitate knowledge sharing, resource optimization, and access to new technologies, ultimately driving innovation and improving service delivery in the biologics contract manufacturing sector.

Scope of the Report

SegmentSub-Segments
By Type

Monoclonal Antibodies

Vaccines

Recombinant Proteins

Cell and Gene Therapies

Blood Products

Biosimilars

Others

By End-User

Pharmaceutical Companies

Biotechnology Firms

Academic and Research Institutions

Contract Research Organizations (CROs)

Others

By Application

Therapeutics

Diagnostics

Research and Development

Others

By Region

China

Japan

India

South Korea

Australia

Southeast Asia (Singapore, Malaysia, Thailand, etc.)

Rest of APAC

By Manufacturing Process

Mammalian Cell Culture

Microbial Fermentation

Upstream Processing

Downstream Processing

Fill and Finish

Others

By Distribution Channel

Direct Sales

Distributors

Online Platforms

Others

By Pricing Model

Cost-Plus Pricing

Value-Based Pricing

Competitive Pricing

Others

Key Target Audience

Investors and Venture Capitalist Firms

Government and Regulatory Bodies (e.g., National Medical Products Administration, Therapeutic Goods Administration)

Biopharmaceutical Manufacturers

Contract Development and Manufacturing Organizations (CDMOs)

Pharmaceutical Supply Chain Managers

Healthcare Providers and Hospitals

Biotechnology Companies

Pharmaceutical Industry Associations

Players Mentioned in the Report:

Samsung Biologics

WuXi Biologics

Lonza Group

Catalent, Inc.

Fujifilm Diosynth Biotechnologies

Boehringer Ingelheim

AGC Biologics

Thermo Fisher Scientific

AbbVie Inc.

Novartis AG

Innovent Biologics

Rentschler Biopharma

JRS Pharma

Probiogen

Toyobo Co., Ltd.

Table of Contents

Market Assessment Phase

1. Executive Summary and Approach


2. APAC Biologics Contract Manufacturing Market Overview

2.1 Key Insights and Strategic Recommendations

2.2 APAC Biologics Contract Manufacturing 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. APAC Biologics Contract Manufacturing Market Analysis

3.1 Growth Drivers

3.1.1 Increasing Demand for Biologics
3.1.2 Advancements in Biomanufacturing Technologies
3.1.3 Rising Investment in Biopharmaceutical R&D
3.1.4 Expanding Healthcare Infrastructure

3.2 Market Challenges

3.2.1 Stringent Regulatory Requirements
3.2.2 High Production Costs
3.2.3 Limited Skilled Workforce
3.2.4 Supply Chain Disruptions

3.3 Market Opportunities

3.3.1 Growth in Biosimilars Market
3.3.2 Strategic Collaborations and Partnerships
3.3.3 Expansion into Emerging Markets
3.3.4 Adoption of Continuous Manufacturing Processes

3.4 Market Trends

3.4.1 Shift Towards Personalized Medicine
3.4.2 Increasing Focus on Sustainability
3.4.3 Digital Transformation in Manufacturing
3.4.4 Rise of Contract Development and Manufacturing Organizations (CDMOs)

3.5 Government Regulation

3.5.1 Regulatory Framework for Biologics
3.5.2 Guidelines for Good Manufacturing Practices (GMP)
3.5.3 Approval Processes for Biologics
3.5.4 Intellectual Property Protection Laws

4. SWOT Analysis


5. Stakeholder Analysis


6. Porter's Five Forces Analysis


7. APAC Biologics Contract Manufacturing Market Market Size, 2019-2024

7.1 By Value

7.2 By Volume

7.3 By Average Selling Price


8. APAC Biologics Contract Manufacturing Market Segmentation

8.1 By Type

8.1.1 Monoclonal Antibodies
8.1.2 Vaccines
8.1.3 Recombinant Proteins
8.1.4 Cell and Gene Therapies
8.1.5 Blood Products
8.1.6 Biosimilars
8.1.7 Others

8.2 By End-User

8.2.1 Pharmaceutical Companies
8.2.2 Biotechnology Firms
8.2.3 Academic and Research Institutions
8.2.4 Contract Research Organizations (CROs)
8.2.5 Others

8.3 By Application

8.3.1 Therapeutics
8.3.2 Diagnostics
8.3.3 Research and Development
8.3.4 Others

8.4 By Region

8.4.1 China
8.4.2 Japan
8.4.3 India
8.4.4 South Korea
8.4.5 Australia
8.4.6 Southeast Asia (Singapore, Malaysia, Thailand, etc.)
8.4.7 Rest of APAC

8.5 By Manufacturing Process

8.5.1 Mammalian Cell Culture
8.5.2 Microbial Fermentation
8.5.3 Upstream Processing
8.5.4 Downstream Processing
8.5.5 Fill and Finish
8.5.6 Others

8.6 By Distribution Channel

8.6.1 Direct Sales
8.6.2 Distributors
8.6.3 Online Platforms
8.6.4 Others

8.7 By Pricing Model

8.7.1 Cost-Plus Pricing
8.7.2 Value-Based Pricing
8.7.3 Competitive Pricing
8.7.4 Others

9. APAC Biologics Contract Manufacturing 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 (CAGR, latest fiscal year)
9.2.4 Market Penetration Rate (Regional/Global client base)
9.2.5 Customer Retention Rate (Annual renewal/contract extension rate)
9.2.6 Operational Efficiency (Batch success rate, lead time, capacity utilization)
9.2.7 Pricing Strategy (Cost leadership, premium, hybrid)
9.2.8 Product Quality Index (Regulatory audit outcomes, batch rejection rate)
9.2.9 Innovation Rate (Patents filed, new service launches, tech adoption)
9.2.10 Supply Chain Efficiency (On-time delivery, raw material sourcing resilience)

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 WuXi Biologics
9.5.3 Lonza Group
9.5.4 Catalent, Inc.
9.5.5 Fujifilm Diosynth Biotechnologies
9.5.6 Boehringer Ingelheim
9.5.7 AGC Biologics
9.5.8 Thermo Fisher Scientific
9.5.9 AbbVie Inc.
9.5.10 Novartis AG
9.5.11 Innovent Biologics
9.5.12 Rentschler Biopharma
9.5.13 JRS Pharma
9.5.14 Probiogen
9.5.15 Toyobo Co., Ltd.

10. APAC Biologics Contract Manufacturing Market End-User Analysis

10.1 Procurement Behavior of Key Ministries

10.1.1 Budget Allocation Trends
10.1.2 Decision-Making Processes
10.1.3 Preferred Contracting Methods
10.1.4 Compliance and Regulatory Considerations

10.2 Corporate Spend on Infrastructure & Energy

10.2.1 Investment Trends in Biologics
10.2.2 Infrastructure Development Initiatives
10.2.3 Energy Efficiency Programs

10.3 Pain Point Analysis by End-User Category

10.3.1 Quality Assurance Challenges
10.3.2 Supply Chain Reliability Issues
10.3.3 Cost Management Concerns

10.4 User Readiness for Adoption

10.4.1 Training and Support Needs
10.4.2 Technology Adoption Barriers

10.5 Post-Deployment ROI and Use Case Expansion

10.5.1 Measurement of ROI
10.5.2 Expansion Opportunities
10.5.3 Long-term Value Realization

11. APAC Biologics Contract Manufacturing 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 Initiatives

7.2 Integrated Supply Chains


8. Key Activities

8.1 Regulatory Compliance

8.2 Branding Efforts

8.3 Distribution Setup


9. Entry Strategy Evaluation

9.1 Domestic Market Entry Strategy

9.1.1 Product Mix Considerations
9.1.2 Pricing Band Strategy
9.1.3 Packaging Solutions

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 for Implementation


12. Control vs Risk Trade-Off

12.1 Ownership Considerations

12.2 Partnerships Evaluation


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

  • Industry reports from regulatory bodies such as the APAC Biologics Association
  • Market analysis publications from leading research firms focusing on biologics
  • Scientific journals and articles detailing advancements in biologics manufacturing technologies

Primary Research

  • Interviews with executives from biologics contract manufacturing organizations (CMOs)
  • Surveys targeting R&D managers in biopharmaceutical companies
  • Focus groups with industry experts and consultants specializing in biologics

Validation & Triangulation

  • Cross-validation of data through multiple industry sources and expert opinions
  • Triangulation of market size estimates using historical growth rates and current trends
  • Sanity checks through feedback from a panel of industry veterans

Phase 2: Market Size Estimation1

Top-down Assessment

  • Analysis of total biopharmaceutical market size and growth rates in the APAC region
  • Segmentation of the market by therapeutic area and type of biologics
  • Incorporation of government funding and initiatives supporting biologics manufacturing

Bottom-up Modeling

  • Data collection from leading CMOs regarding their production capacities and output
  • Cost analysis based on operational expenses and pricing models of biologics
  • Volume estimates derived from client contracts and production schedules

Forecasting & Scenario Analysis

  • Multi-variable regression analysis incorporating market drivers such as aging population and disease prevalence
  • Scenario planning based on potential regulatory changes and technological advancements
  • Development of baseline, optimistic, and pessimistic forecasts through 2030

Phase 3: CATI Sample Composition1

Scope Item/SegmentSample SizeTarget Respondent Profiles
Biologics Manufacturing Capacity60Operations Managers, Production Directors
Regulatory Compliance in Biologics50Quality Assurance Managers, Regulatory Affairs Specialists
Market Trends in Biologics40Market Analysts, Business Development Managers
Investment in Biologics R&D45R&D Directors, Financial Analysts
Client Satisfaction with CMO Services50Procurement Officers, Project Managers

Frequently Asked Questions

What is the current value of the APAC Biologics Contract Manufacturing Market?

The APAC Biologics Contract Manufacturing Market is valued at approximately USD 11.7 billion, driven by increasing demand for biologics, advancements in biomanufacturing technologies, and the rising prevalence of chronic diseases.

Which countries dominate the APAC Biologics Contract Manufacturing Market?

What are the key growth drivers for the APAC Biologics Contract Manufacturing Market?

What challenges does the APAC Biologics Contract Manufacturing Market face?

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