의약품 수탁개발제조 시장 : 서비스, 개발 단계, 최종 사용자별 - 세계 예측(2025-2030년)

The Pharmaceutical Contract Development & Manufacturing Market was valued at USD 125.73 billion in 2023, expected to reach USD 136.27 billion in 2024, and is projected to grow at a CAGR of 8.46%, to USD 222.04 billion by 2030.

The pharmaceutical contract development and manufacturing (CDMO) industry serves as a critical component in the healthcare supply chain, providing essential services such as drug development, manufacturing, and packaging to pharmaceutical companies of all sizes. Its necessity stems from the increasing need for pharmaceutical firms to focus on their core competencies while leveraging CDMO expertise to streamline product innovation and bring drugs to market more efficiently. The application scope of CDMOs spans the entire drug production lifecycle, including synthesis, formulation, clinical trials, and commercial manufacturing. Key end-use segments include large pharma companies, biotech firms, and generic drug producers. Market growth is fueled by factors such as rising demand for biologics and biosimilars, the pressure to reduce drug development time, and an increase in outsourcing activities driven by the need for specialized manufacturing capabilities. Recent opportunities include expanding capabilities in cell and gene therapies, leveraging artificial intelligence for process optimization, and forming strategic partnerships to enhance service offerings. However, the market faces challenges such as stringent regulatory requirements, high initial investment costs, and supply chain disruptions impacting production timelines.

To capture emerging opportunities, CDMOs should focus on expanding their offerings in personalized medicine and regenerative therapies, invest in cutting-edge manufacturing technologies like continuous processing and 3D printing, and develop robust data analytics capabilities for improved decision-making. Moreover, forming alliances with technology providers can help overcome some technological challenges faced by the sector. Limitations are often related to the high capital expenditure required for advanced manufacturing infrastructure and maintaining compliance with global regulatory standards. The CDMO market is inherently dynamic, characterized by rapid technological advancements and evolving client demands, making it critical for companies to remain agile and forward-thinking. Continuous investment in R&D and innovation, paired with strategic partnerships, can position CDMOs for sustained growth while navigating existing and emerging challenges.

Market Dynamics: Unveiling Key Market Insights in the Rapidly Evolving Pharmaceutical Contract Development & Manufacturing Market

The Pharmaceutical Contract Development & Manufacturing Market is undergoing transformative changes driven by a dynamic interplay of supply and demand factors. Understanding these evolving market dynamics prepares business organizations to make informed investment decisions, refine strategic decisions, and seize new opportunities. By gaining a comprehensive view of these trends, business organizations can mitigate various risks across political, geographic, technical, social, and economic domains while also gaining a clearer understanding of consumer behavior and its impact on manufacturing costs and purchasing trends.

• Market Drivers
  • Rising Demand for Generics and Biological Therapies
  • Increasing Investments in Pharmaceutical R&D
  • Increasing Number of CDMOs and Rising Investments in Advanced Manufacturing Technologies by CDMOs
• Market Restraints
  • Introduction of Serialization
• Market Opportunities
  • Increasing Focus on Nuclear Medicine and Specialty Drugs
  • Growing need for Cell and Gene Therapies
• Market Challenges
  • Variable Trade Policies Between Countries

Porter's Five Forces: A Strategic Tool for Navigating the Pharmaceutical Contract Development & Manufacturing Market

Porter's five forces framework is a critical tool for understanding the competitive landscape of the Pharmaceutical Contract Development & Manufacturing Market. It offers business organizations with a clear methodology for evaluating their competitive positioning and exploring strategic opportunities. This framework helps businesses assess the power dynamics within the market and determine the profitability of new ventures. With these insights, business organizations can leverage their strengths, address weaknesses, and avoid potential challenges, ensuring a more resilient market positioning.

PESTLE Analysis: Navigating External Influences in the Pharmaceutical Contract Development & Manufacturing Market

External macro-environmental factors play a pivotal role in shaping the performance dynamics of the Pharmaceutical Contract Development & Manufacturing Market. Political, Economic, Social, Technological, Legal, and Environmental factors analysis provides the necessary information to navigate these influences. By examining PESTLE factors, businesses can better understand potential risks and opportunities. This analysis enables business organizations to anticipate changes in regulations, consumer preferences, and economic trends, ensuring they are prepared to make proactive, forward-thinking decisions.

Market Share Analysis: Understanding the Competitive Landscape in the Pharmaceutical Contract Development & Manufacturing Market

A detailed market share analysis in the Pharmaceutical Contract Development & Manufacturing Market provides a comprehensive assessment of vendors' performance. Companies can identify their competitive positioning by comparing key metrics, including revenue, customer base, and growth rates. This analysis highlights market concentration, fragmentation, and trends in consolidation, offering vendors the insights required to make strategic decisions that enhance their position in an increasingly competitive landscape.

FPNV Positioning Matrix: Evaluating Vendors' Performance in the Pharmaceutical Contract Development & Manufacturing Market

The Forefront, Pathfinder, Niche, Vital (FPNV) Positioning Matrix is a critical tool for evaluating vendors within the Pharmaceutical Contract Development & Manufacturing Market. This matrix enables business organizations to make well-informed decisions that align with their goals by assessing vendors based on their business strategy and product satisfaction. The four quadrants provide a clear and precise segmentation of vendors, helping users identify the right partners and solutions that best fit their strategic objectives.

Strategy Analysis & Recommendation: Charting a Path to Success in the Pharmaceutical Contract Development & Manufacturing Market

A strategic analysis of the Pharmaceutical Contract Development & Manufacturing Market is essential for businesses looking to strengthen their global market presence. By reviewing key resources, capabilities, and performance indicators, business organizations can identify growth opportunities and work toward improvement. This approach helps businesses navigate challenges in the competitive landscape and ensures they are well-positioned to capitalize on newer opportunities and drive long-term success.

Key Company Profiles

The report delves into recent significant developments in the Pharmaceutical Contract Development & Manufacturing Market, highlighting leading vendors and their innovative profiles. These include AbbVie, Inc., Acino International AG, Aenova Holding GmbH, Akums Drugs& Pharmaceuticals Ltd, Almac Group Limited, Aurobindo Pharma Limited, Boehringer Ingelheim International GmbH, Cambrex Corporation, Catalent, Inc., Curia Global, Inc., Danaher Corporation, Delwis Healthcare Pvt. Ltd., Evonik Industries AG, Fabbrica Italiana Sintetici S.p.A., Famar Health Care Services, FUJIFILM Diosynth Biotechnologies U.S.A., Inc., Gerresheimer AG, Grifols S.A., Hikal Ltd, Hovione, Jubilant Pharmova Limited, Lonza Group AG, Pfizer Inc., Porton Pharma Solutions Ltd., Recipharm AB, Samsung Biologics Co., Ltd., Siegfried AG, The Fareva Group, Thermo Fisher Scientific Inc., Vetter Pharma-Fertigung GmbH & Co. KG, and WuXi Biologics Co., Ltd..

Market Segmentation & Coverage

This research report categorizes the Pharmaceutical Contract Development & Manufacturing Market to forecast the revenues and analyze trends in each of the following sub-markets:

• Based on Service, market is studied across Biologics Manufacturing Services, Drug Development Services, Pharmaceutical Manufacturing Services, and Secondary Packaging Services. The Biologics Manufacturing Services is further studied across Biologics API Manufacturing Services and Biologics FDF Manufacturing Services. The Pharmaceutical Manufacturing Services is further studied across Pharmaceutical API Manufacturing and Pharmaceutical FDF Manufacturing. The Pharmaceutical API Manufacturing is further studied across Capsule Manufacturing Services, Oral Liquid Manufacturing Services, Parenteral/Injectable Manufacturing Services, and Tablet Manufacturing Services.
• Based on Development Stage, market is studied across Phase I Clinical Trials, Phase II Clinical Trials, Phase III Clinical Trials, Phase IV Clinical Trials, and Preclinical.
• Based on End User, market is studied across Biotechnology Companies, Generic Pharmaceutical Companies, Pharmaceutical Companies, and Small & Mid-Size Pharma. The Pharmaceutical Companies is further studied across Big Pharma and Specialty Pharma.
• Based on Region, market is studied across Americas, Asia-Pacific, and Europe, Middle East & Africa. The Americas is further studied across Argentina, Brazil, Canada, Mexico, and United States. The United States is further studied across California, Florida, Illinois, New York, Ohio, Pennsylvania, and Texas. The Asia-Pacific is further studied across Australia, China, India, Indonesia, Japan, Malaysia, Philippines, Singapore, South Korea, Taiwan, Thailand, and Vietnam. The Europe, Middle East & Africa is further studied across Denmark, Egypt, Finland, France, Germany, Israel, Italy, Netherlands, Nigeria, Norway, Poland, Qatar, Russia, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, and United Kingdom.

The report offers a comprehensive analysis of the market, covering key focus areas:

1. Market Penetration: A detailed review of the current market environment, including extensive data from top industry players, evaluating their market reach and overall influence.

2. Market Development: Identifies growth opportunities in emerging markets and assesses expansion potential in established sectors, providing a strategic roadmap for future growth.

3. Market Diversification: Analyzes recent product launches, untapped geographic regions, major industry advancements, and strategic investments reshaping the market.

4. Competitive Assessment & Intelligence: Provides a thorough analysis of the competitive landscape, examining market share, business strategies, product portfolios, certifications, regulatory approvals, patent trends, and technological advancements of key players.

5. Product Development & Innovation: Highlights cutting-edge technologies, R&D activities, and product innovations expected to drive future market growth.

The report also answers critical questions to aid stakeholders in making informed decisions:

1. What is the current market size, and what is the forecasted growth?

2. Which products, segments, and regions offer the best investment opportunities?

3. What are the key technology trends and regulatory influences shaping the market?

4. How do leading vendors rank in terms of market share and competitive positioning?

5. What revenue sources and strategic opportunities drive vendors' market entry or exit strategies?

Table of Contents

1. Preface

• 1.1. Objectives of the Study
• 1.2. Market Segmentation & Coverage
• 1.3. Years Considered for the Study
• 1.4. Currency & Pricing
• 1.5. Language
• 1.6. Stakeholders

2. Research Methodology

• 2.1. Define: Research Objective
• 2.2. Determine: Research Design
• 2.3. Prepare: Research Instrument
• 2.4. Collect: Data Source
• 2.5. Analyze: Data Interpretation
• 2.6. Formulate: Data Verification
• 2.7. Publish: Research Report
• 2.8. Repeat: Report Update

3. Executive Summary

4. Market Overview

5. Market Insights

• 5.1. Market Dynamics
  • 5.1.1. Drivers
    • 5.1.1.1. Rising Demand for Generics and Biological Therapies
    • 5.1.1.2. Increasing Investments in Pharmaceutical R&D
    • 5.1.1.3. Increasing Number of CDMOs and Rising Investments in Advanced Manufacturing Technologies by CDMOs
  • 5.1.2. Restraints
    • 5.1.2.1. Introduction of Serialization
  • 5.1.3. Opportunities
    • 5.1.3.1. Increasing Focus on Nuclear Medicine and Specialty Drugs
    • 5.1.3.2. Growing need for Cell and Gene Therapies
  • 5.1.4. Challenges
    • 5.1.4.1. Variable Trade Policies Between Countries
• 5.2. Market Segmentation Analysis
  • 5.2.1. Service: Rising penetration of biologics manufacturing services by end-users to adhere to stringent regulatory standards
  • 5.2.2. End User: Big pharma companies widely adopting pharmaceutical CDMO services to manage complex drug development
• 5.3. Porter's Five Forces Analysis
  • 5.3.1. Threat of New Entrants
  • 5.3.2. Threat of Substitutes
  • 5.3.3. Bargaining Power of Customers
  • 5.3.4. Bargaining Power of Suppliers
  • 5.3.5. Industry Rivalry
• 5.4. PESTLE Analysis
  • 5.4.1. Political
  • 5.4.2. Economic
  • 5.4.3. Social
  • 5.4.4. Technological
  • 5.4.5. Legal
  • 5.4.6. Environmental

6. Pharmaceutical Contract Development & Manufacturing Market, by Service

• 6.1. Introduction
• 6.2. Biologics Manufacturing Services
  • 6.2.1. Biologics API Manufacturing Services
  • 6.2.2. Biologics FDF Manufacturing Services
• 6.3. Drug Development Services
• 6.4. Pharmaceutical Manufacturing Services
  • 6.4.1. Pharmaceutical API Manufacturing
    • 6.4.1.1. Capsule Manufacturing Services
    • 6.4.1.2. Oral Liquid Manufacturing Services
    • 6.4.1.3. Parenteral/Injectable Manufacturing Services
    • 6.4.1.4. Tablet Manufacturing Services
  • 6.4.2. Pharmaceutical FDF Manufacturing
• 6.5. Secondary Packaging Services

7. Pharmaceutical Contract Development & Manufacturing Market, by Development Stage

• 7.1. Introduction
• 7.2. Phase I Clinical Trials
• 7.3. Phase II Clinical Trials
• 7.4. Phase III Clinical Trials
• 7.5. Phase IV Clinical Trials
• 7.6. Preclinical

8. Pharmaceutical Contract Development & Manufacturing Market, by End User

• 8.1. Introduction
• 8.2. Biotechnology Companies
• 8.3. Generic Pharmaceutical Companies
• 8.4. Pharmaceutical Companies
  • 8.4.1. Big Pharma
  • 8.4.2. Specialty Pharma
• 8.5. Small & Mid-Size Pharma

9. Americas Pharmaceutical Contract Development & Manufacturing Market

• 9.1. Introduction
• 9.2. Argentina
• 9.3. Brazil
• 9.4. Canada
• 9.5. Mexico
• 9.6. United States

10. Asia-Pacific Pharmaceutical Contract Development & Manufacturing Market

• 10.1. Introduction
• 10.2. Australia
• 10.3. China
• 10.4. India
• 10.5. Indonesia
• 10.6. Japan
• 10.7. Malaysia
• 10.8. Philippines
• 10.9. Singapore
• 10.10. South Korea
• 10.11. Taiwan
• 10.12. Thailand
• 10.13. Vietnam

11. Europe, Middle East & Africa Pharmaceutical Contract Development & Manufacturing Market

• 11.1. Introduction
• 11.2. Denmark
• 11.3. Egypt
• 11.4. Finland
• 11.5. France
• 11.6. Germany
• 11.7. Israel
• 11.8. Italy
• 11.9. Netherlands
• 11.10. Nigeria
• 11.11. Norway
• 11.12. Poland
• 11.13. Qatar
• 11.14. Russia
• 11.15. Saudi Arabia
• 11.16. South Africa
• 11.17. Spain
• 11.18. Sweden
• 11.19. Switzerland
• 11.20. Turkey
• 11.21. United Arab Emirates
• 11.22. United Kingdom

12. Competitive Landscape

• 12.1. Market Share Analysis, 2023
• 12.2. FPNV Positioning Matrix, 2023
• 12.3. Competitive Scenario Analysis
  • 12.3.1. AGC Biologics and BioConnection join forces to provide end-to-end biopharmaceutical development and manufacturing solutions, enhancing efficiency and speeding up market delivery.
  • 12.3.2. Kuhne Holding AG acquires majority stake in Aenova Group from BC Partners, leveraging resources for enhanced growth and innovation
  • 12.3.3. Alcami Announces Acquisition of West-Coast-Based Pacific Pharmaceutical Services
  • 12.3.4. Piramal Pharma to Invest INR 1,000 Crore for Expansion
  • 12.3.5. eXmoor Pharma Expands into Full-Service Cell and Gene Therapy CDMO Partner with Opening of GMP Facilities
• 12.4. Strategy Analysis & Recommendation

Companies Mentioned

• 1. AbbVie, Inc.
• 2. Acino International AG
• 3. Aenova Holding GmbH
• 4. Akums Drugs& Pharmaceuticals Ltd
• 5. Almac Group Limited
• 6. Aurobindo Pharma Limited
• 7. Boehringer Ingelheim International GmbH
• 8. Cambrex Corporation
• 9. Catalent, Inc.
• 10. Curia Global, Inc.
• 11. Danaher Corporation
• 12. Delwis Healthcare Pvt. Ltd.
• 13. Evonik Industries AG
• 14. Fabbrica Italiana Sintetici S.p.A.
• 15. Famar Health Care Services
• 16. FUJIFILM Diosynth Biotechnologies U.S.A., Inc.
• 17. Gerresheimer AG
• 18. Grifols S.A.
• 19. Hikal Ltd
• 20. Hovione
• 21. Jubilant Pharmova Limited
• 22. Lonza Group AG
• 23. Pfizer Inc.
• 24. Porton Pharma Solutions Ltd.
• 25. Recipharm AB
• 26. Samsung Biologics Co., Ltd.
• 27. Siegfried AG
• 28. The Fareva Group
• 29. Thermo Fisher Scientific Inc.
• 30. Vetter Pharma-Fertigung GmbH & Co. KG
• 31. WuXi Biologics Co., Ltd.