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Indonesia pharmaceutical cdmo market report Size, Share, Growth Drivers, Trends, Opportunities & Forecast 2025–2030

Indonesia Pharmaceutical CDMO Market, valued at USD 10 Bn, grows due to rising generic drug demand, healthcare expenditure, and biopharma expansion, supported by GMP regulations and local investments.

Region:Asia

Author(s):Rebecca

Product Code:KRAC3171

Pages:96

Published On:October 2025

About the Report

Base Year 2024

Indonesia Pharmaceutical CDMO Market Overview

  • The Indonesia Pharmaceutical CDMO Market is valued at USD 10 billion, based on a five-year historical analysis. This growth is primarily driven by the increasing demand for contract manufacturing services, particularly in the production of generic drugs and biologics, as well as the rising focus on cost-effective manufacturing solutions by pharmaceutical companies. Additional growth drivers include the expansion of biologics production, rising demand for personalized medicine, and the adoption of advanced manufacturing technologies such as continuous manufacturing and digital integration. Small and mid-sized pharmaceutical firms are increasingly outsourcing to CDMOs to accelerate product launches and navigate regulatory complexities .
  • Key cities such as Jakarta, Bandung, and Surabaya dominate the market due to their robust infrastructure, availability of skilled labor, and proximity to major pharmaceutical companies. Jakarta, being the capital, serves as a central hub for business operations and regulatory activities, while Bandung and Surabaya contribute significantly to manufacturing capabilities. These cities benefit from government initiatives to enhance healthcare infrastructure and attract foreign investment, further supporting market growth .
  • In 2023, the Indonesian government implemented the "National Health Insurance Program," which mandates that all pharmaceutical products must comply with Good Manufacturing Practices (GMP). This regulation is enforced under the Regulation of the Minister of Health of the Republic of Indonesia No. 34 of 2018 concerning Good Manufacturing Practice for Pharmaceutical Products, issued by the Ministry of Health. The regulation covers all pharmaceutical manufacturers, requiring compliance with GMP standards for product quality and safety, and includes operational requirements for facility standards, documentation, and quality control. This has significantly boosted demand for CDMO services that meet these stringent standards .
Indonesia Pharmaceutical CDMO Market Size

Indonesia Pharmaceutical CDMO Market Segmentation

By Type:The market can be segmented into various types, including Active Pharmaceutical Ingredients (APIs), Finished Dosage Forms, Biologics, Contract Packaging Services, Sterile Injectables, and Others. Each segment plays a crucial role in market dynamics:

Indonesia Pharmaceutical CDMO Market segmentation by Type.
  • Active Pharmaceutical Ingredients (APIs):CDMOs provide synthesis, scale-up, and regulatory support for APIs, which are essential for both generic and innovative drugs.
  • Finished Dosage Forms:Includes tablets, capsules, and other oral or injectable products, with CDMOs offering formulation, manufacturing, and packaging services.
  • Biologics:Encompasses monoclonal antibodies, recombinant proteins, and vaccines, with Indonesia's biologics segment rapidly expanding due to increased demand for advanced therapies .
  • Contract Packaging Services:CDMOs provide secondary packaging, labeling, serialization, and logistics support to ensure regulatory compliance and market readiness.
  • Sterile Injectables:Specialized manufacturing for injectable drugs, requiring stringent aseptic conditions and regulatory oversight .
  • Others:Includes niche services such as clinical trial material supply, analytical testing, and specialty formulations.

By End-User:The end-user segmentation includes Pharmaceutical Companies, Biotechnology Firms, Research Institutions, Medical Device Companies, and Others. Each end-user group has distinct requirements:

Indonesia Pharmaceutical CDMO Market segmentation by End-User.
  • Pharmaceutical Companies:Major drivers of CDMO demand, outsourcing manufacturing and development to optimize costs and focus on R&D.
  • Biotechnology Firms:Increasingly rely on CDMOs for specialized biologics and biosimilars production, benefiting from advanced capabilities and regulatory expertise.
  • Research Institutions:Collaborate with CDMOs for clinical trial material production, analytical testing, and pilot-scale manufacturing.
  • Medical Device Companies:Utilize CDMO services for combination products, packaging, and regulatory support.
  • Others:Includes government agencies, non-profit organizations, and specialty healthcare providers seeking tailored CDMO solutions.

Indonesia Pharmaceutical CDMO Market Competitive Landscape

The Indonesia Pharmaceutical CDMO Market is characterized by a dynamic mix of regional and international players. Leading participants such as PT Kalbe Farma Tbk, PT Kimia Farma Tbk, PT Indofarma Tbk, PT Dexa Medica, PT Sanbe Farma, PT Merck Tbk, PT Novell Pharmaceutical Laboratories, PT Soho Global Health, PT Harsen Laboratories, PT Bio Farma (Persero), PT Indofarma Global Medika, PT Anugerah Pharmindo Lestari, PT Mersifarma Tirmaku Mercusana, PT Darya-Varia Laboratoria Tbk, PT Sido Muncul Tbk contribute to innovation, geographic expansion, and service delivery in this space.

PT Kalbe Farma Tbk

1966

Jakarta, Indonesia

PT Kimia Farma Tbk

1817

Jakarta, Indonesia

PT Indofarma Tbk

1971

Jakarta, Indonesia

PT Dexa Medica

1969

Tangerang, Indonesia

PT Sanbe Farma

1975

Bandung, Indonesia

Company

Establishment Year

Headquarters

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

Revenue (USD Million)

Revenue Growth Rate (%)

Market Share (%)

Number of Manufacturing Facilities

Regulatory Certifications (e.g., GMP, WHO, PIC/S)

Indonesia Pharmaceutical CDMO Market Industry Analysis

Growth Drivers

  • Increasing Demand for Generic Drugs:The Indonesian pharmaceutical market is witnessing a significant rise in the demand for generic drugs, driven by a growing population of approximately 270 million. In future, the generic drug market is projected to reach IDR 55 trillion, reflecting a 10% increase from the previous year. This surge is attributed to the rising prevalence of chronic diseases and the government's push for affordable healthcare solutions, making generics a vital component of the healthcare system.
  • Rising Healthcare Expenditure:Indonesia's healthcare expenditure is expected to reach IDR 550 trillion in future, up from IDR 500 trillion in the previous year. This increase is driven by the government's commitment to improving healthcare access and quality, particularly through the National Health Insurance program. As healthcare spending rises, pharmaceutical companies are likely to invest more in contract development and manufacturing organizations (CDMOs) to meet the growing demand for innovative and cost-effective drug solutions.
  • Expansion of Biopharmaceuticals:The biopharmaceutical sector in Indonesia is projected to grow significantly, with an estimated market value of IDR 25 trillion by future. This growth is fueled by advancements in biotechnology and an increasing focus on personalized medicine. The government is also supporting this expansion through initiatives aimed at enhancing local production capabilities, which will further drive demand for CDMO services in the biopharmaceutical space.

Market Challenges

  • Regulatory Compliance Issues:Navigating the complex regulatory landscape in Indonesia poses a significant challenge for CDMOs. The country has stringent regulations that require compliance with Good Manufacturing Practices (GMP) and other standards. In future, the cost of compliance is expected to rise by 15%, impacting operational efficiency. This complexity can deter foreign investments and slow down the growth of local CDMOs, limiting their competitiveness in the global market.
  • High Competition from Global Players:The Indonesian pharmaceutical CDMO market faces intense competition from established global players, which can hinder the growth of local companies. In future, it is estimated that foreign CDMOs will capture approximately 45% of the market share, leveraging their advanced technologies and established reputations. This competitive pressure may lead to price wars, further squeezing profit margins for local CDMOs and challenging their sustainability.

Indonesia Pharmaceutical CDMO Market Future Outlook

The future of the Indonesian pharmaceutical CDMO market appears promising, driven by increasing investments in healthcare infrastructure and a growing emphasis on local manufacturing. As the government continues to support initiatives aimed at enhancing production capabilities, local CDMOs are expected to expand their service offerings. Additionally, the integration of digital technologies and AI in drug development will likely streamline processes, improve efficiency, and foster innovation, positioning Indonesia as a competitive player in the global pharmaceutical landscape.

Market Opportunities

  • Growth in Export Markets:With the increasing quality of locally manufactured pharmaceuticals, Indonesian CDMOs have the opportunity to tap into export markets. In future, exports are projected to reach IDR 12 trillion, driven by demand from neighboring countries. This expansion can enhance revenue streams and establish Indonesia as a regional hub for pharmaceutical manufacturing.
  • Collaborations with Research Institutions:Collaborating with local research institutions presents a significant opportunity for CDMOs to innovate and develop new products. In future, partnerships are expected to increase by 25%, facilitating knowledge transfer and access to cutting-edge research. This collaboration can enhance the capabilities of CDMOs, enabling them to offer more specialized services and products to the market.

Scope of the Report

SegmentSub-Segments
By Type

Active Pharmaceutical Ingredients (APIs)

Finished Dosage Forms

Biologics

Contract Packaging Services

Sterile Injectables

Others

By End-User

Pharmaceutical Companies

Biotechnology Firms

Research Institutions

Medical Device Companies

Others

By Application

Oncology

Cardiovascular

Infectious Diseases

Metabolic Disorders

Others

By Distribution Channel

Direct Sales

Online Platforms

Distributors

Retail Sales

Others

By Regulatory Compliance Level

GMP Compliant

Non-GMP Compliant

Others

By Product Lifecycle Stage

Development Stage

Commercial Stage

Others

By Market Maturity

Emerging Market

Established Market

Others

Key Target Audience

Investors and Venture Capitalist Firms

Government and Regulatory Bodies (e.g., Badan Pengawas Obat dan Makanan - BPOM)

Pharmaceutical Manufacturers

Biotechnology Companies

Contract Research Organizations (CROs)

Supply Chain and Logistics Providers

Pharmaceutical Industry Associations

Healthcare Providers and Institutions

Players Mentioned in the Report:

PT Kalbe Farma Tbk

PT Kimia Farma Tbk

PT Indofarma Tbk

PT Dexa Medica

PT Sanbe Farma

PT Merck Tbk

PT Novell Pharmaceutical Laboratories

PT Soho Global Health

PT Harsen Laboratories

PT Bio Farma (Persero)

PT Indofarma Global Medika

PT Anugerah Pharmindo Lestari

PT Mersifarma Tirmaku Mercusana

PT Darya-Varia Laboratoria Tbk

PT Sido Muncul Tbk

Table of Contents

Market Assessment Phase

1. Executive Summary and Approach


2. Indonesia Pharmaceutical CDMO Market Overview

2.1 Key Insights and Strategic Recommendations

2.2 Indonesia Pharmaceutical 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. Indonesia Pharmaceutical CDMO Market Analysis

3.1 Growth Drivers

3.1.1 Increasing Demand for Generic Drugs
3.1.2 Rising Healthcare Expenditure
3.1.3 Expansion of Biopharmaceuticals
3.1.4 Government Initiatives for Local Manufacturing

3.2 Market Challenges

3.2.1 Regulatory Compliance Issues
3.2.2 High Competition from Global Players
3.2.3 Limited Access to Advanced Technologies
3.2.4 Supply Chain Disruptions

3.3 Market Opportunities

3.3.1 Growth in Export Markets
3.3.2 Collaborations with Research Institutions
3.3.3 Adoption of Digital Technologies
3.3.4 Increasing Focus on Sustainable Practices

3.4 Market Trends

3.4.1 Shift Towards Contract Manufacturing
3.4.2 Rise of Personalized Medicine
3.4.3 Integration of AI in Drug Development
3.4.4 Emphasis on Quality Assurance

3.5 Government Regulation

3.5.1 Implementation of Good Manufacturing Practices (GMP)
3.5.2 Regulatory Framework for Biologics
3.5.3 Policies Supporting Local Production
3.5.4 Import Regulations for Pharmaceutical Ingredients

4. SWOT Analysis


5. Stakeholder Analysis


6. Porter's Five Forces Analysis


7. Indonesia Pharmaceutical CDMO Market Market Size, 2019-2024

7.1 By Value

7.2 By Volume

7.3 By Average Selling Price


8. Indonesia Pharmaceutical CDMO Market Segmentation

8.1 By Type

8.1.1 Active Pharmaceutical Ingredients (APIs)
8.1.2 Finished Dosage Forms
8.1.3 Biologics
8.1.4 Contract Packaging Services
8.1.5 Sterile Injectables
8.1.6 Others

8.2 By End-User

8.2.1 Pharmaceutical Companies
8.2.2 Biotechnology Firms
8.2.3 Research Institutions
8.2.4 Medical Device Companies
8.2.5 Others

8.3 By Application

8.3.1 Oncology
8.3.2 Cardiovascular
8.3.3 Infectious Diseases
8.3.4 Metabolic Disorders
8.3.5 Others

8.4 By Distribution Channel

8.4.1 Direct Sales
8.4.2 Online Platforms
8.4.3 Distributors
8.4.4 Retail Sales
8.4.5 Others

8.5 By Regulatory Compliance Level

8.5.1 GMP Compliant
8.5.2 Non-GMP Compliant
8.5.3 Others

8.6 By Product Lifecycle Stage

8.6.1 Development Stage
8.6.2 Commercial Stage
8.6.3 Others

8.7 By Market Maturity

8.7.1 Emerging Market
8.7.2 Established Market
8.7.3 Others

9. Indonesia Pharmaceutical 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 (USD Million)
9.2.4 Revenue Growth Rate (%)
9.2.5 Market Share (%)
9.2.6 Number of Manufacturing Facilities
9.2.7 Regulatory Certifications (e.g., GMP, WHO, PIC/S)
9.2.8 Capacity Utilization Rate (%)
9.2.9 R&D Investment as % of Revenue
9.2.10 Number of CDMO Service Offerings
9.2.11 Major Client Segments
9.2.12 Export Ratio (%)
9.2.13 Innovation Index
9.2.14 Supply Chain Lead Time (Days)
9.2.15 Customer Retention Rate (%)

9.3 SWOT Analysis of Top Players

9.4 Pricing Analysis

9.5 Detailed Profile of Major Companies

9.5.1 PT Kalbe Farma Tbk
9.5.2 PT Kimia Farma Tbk
9.5.3 PT Indofarma Tbk
9.5.4 PT Dexa Medica
9.5.5 PT Sanbe Farma
9.5.6 PT Merck Tbk
9.5.7 PT Novell Pharmaceutical Laboratories
9.5.8 PT Soho Global Health
9.5.9 PT Harsen Laboratories
9.5.10 PT Bio Farma (Persero)
9.5.11 PT Indofarma Global Medika
9.5.12 PT Anugerah Pharmindo Lestari
9.5.13 PT Mersifarma Tirmaku Mercusana
9.5.14 PT Darya-Varia Laboratoria Tbk
9.5.15 PT Sido Muncul Tbk

10. Indonesia Pharmaceutical CDMO Market End-User Analysis

10.1 Procurement Behavior of Key Ministries

10.1.1 Ministry of Health
10.1.2 Ministry of Industry
10.1.3 Ministry of Research and Technology

10.2 Corporate Spend on Infrastructure & Energy

10.2.1 Pharmaceutical Infrastructure Investments
10.2.2 Energy Efficiency Initiatives

10.3 Pain Point Analysis by End-User Category

10.3.1 Quality Assurance Challenges
10.3.2 Supply Chain Reliability Issues

10.4 User Readiness for Adoption

10.4.1 Technology Adoption Rates
10.4.2 Training and Development Needs

10.5 Post-Deployment ROI and Use Case Expansion

10.5.1 ROI Measurement Techniques
10.5.2 Use Case Development Opportunities

11. Indonesia Pharmaceutical 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 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 Strategies


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 local and international pharmaceutical associations
  • Review of government publications and regulatory frameworks affecting the pharmaceutical sector in Indonesia
  • Examination of market trends and forecasts from reputable market research firms

Primary Research

  • Interviews with executives from leading Contract Development and Manufacturing Organizations (CDMOs) in Indonesia
  • Surveys targeting pharmaceutical companies to understand outsourcing trends and preferences
  • Field interviews with regulatory experts to assess compliance challenges faced by CDMOs

Validation & Triangulation

  • Cross-validation of findings through multiple data sources including trade publications and expert opinions
  • Triangulation of market size estimates using both top-down and bottom-up approaches
  • Sanity checks through feedback from industry panels and focus groups

Phase 2: Market Size Estimation1

Top-down Assessment

  • Estimation of the overall pharmaceutical market size in Indonesia as a basis for CDMO market potential
  • Segmentation of the market by therapeutic areas and types of pharmaceutical products
  • Incorporation of growth rates from historical data and projected industry trends

Bottom-up Modeling

  • Collection of data on production capacities and output from key CDMOs operating in Indonesia
  • Analysis of service pricing models and cost structures of CDMOs
  • Volume estimates based on client contracts and project pipelines within the CDMO sector

Forecasting & Scenario Analysis

  • Development of forecasting models based on macroeconomic indicators and healthcare spending trends
  • Scenario analysis considering potential regulatory changes and market entry of new players
  • Creation of baseline, optimistic, and pessimistic forecasts through 2030

Phase 3: CATI Sample Composition1

Scope Item/SegmentSample SizeTarget Respondent Profiles
Pharmaceutical CDMO Services100Operations Managers, Business Development Executives
Regulatory Compliance Insights60Regulatory Affairs Specialists, Quality Assurance Managers
Market Entry Strategies40Strategic Planners, Market Analysts
Client Satisfaction and Feedback80Pharmaceutical Company Executives, Procurement Officers
Trends in Outsourcing50Supply Chain Managers, R&D Directors

Frequently Asked Questions

What is the current value of the Indonesia Pharmaceutical CDMO Market?

The Indonesia Pharmaceutical CDMO Market is valued at approximately USD 10 billion, driven by the increasing demand for contract manufacturing services, particularly in generic drugs and biologics, as well as the focus on cost-effective manufacturing solutions.

What are the key growth drivers for the Indonesia Pharmaceutical CDMO Market?

Which cities are the main hubs for the Indonesia Pharmaceutical CDMO Market?

What regulatory changes have impacted the Indonesia Pharmaceutical CDMO Market?

Other Regional/Country Reports

Malaysia Pharmaceutical CDMO Market

KSA Pharmaceutical CDMO Market

APAC Pharmaceutical CDMO Market

SEA Pharmaceutical CDMO Market

Vietnam Pharmaceutical CDMO Market

Thailand Pharmaceutical CDMO Market

Other Adjacent Reports

Philippines Generic Drugs Market

Qatar Biopharmaceutical Market

KSA Active Pharmaceutical Ingredients Market

Germany Finished Dosage Forms Market

South Korea Biologics Market

Oman Contract Packaging Services Market

Brazil Sterile Injectables Market

Oman Pharmaceutical Export Market

Germany Healthcare Expenditure Market

KSA Biotechnology Services Market

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