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合约开发和製造组织市场 - 全球行业规模、份额、趋势、机会和预测，按服务类型 CMO、研究阶段 CRO、地区和竞争细分，2019-2029F

Contract Development and Manufacturing Organization Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Service Type CMO, By Research Phase CRO, By Region and Competition, 2019-2029F

出版日期: 2024年11月30日 | 出版商:

TechSci Research | 英文 183 Pages | 商品交期: 2-3个工作天内

价格

简介目录

2023年全球合约开发和製造组织市场价值为2,401.9亿美元，预计到2029年将达到3,466.9亿美元，预测期内复合年增长率为6.48%。

市场概况
预测期	2025-2029
2023 年市场规模	2401.9亿美元
2029 年市场规模	3466.9亿美元
2024-2029 年复合年增长率	6.48%
成长最快的细分市场	成品剂型 (FDF) 开发製造
最大的市场	北美洲

全球合约开发和製造组织 (CDMO) 市场是製药和生物技术行业中快速增长的部分，受到与药物开发和製造相关的外包服务需求不断增长的推动。 CDMO 提供广泛的服务，包括药物配方、临床试验材料生产、放大生产和商业生产。随着製药公司寻求降低成本、提高效率并专注于核心竞争力，同时外包生产和开发等非核心职能，这个市场已经扩大。促进市场成长的关键因素包括药物配方日益复杂、对生物製剂和生物相似药的需求不断增加以及对专业製造能力的需求，特别是在无菌和高效药物领域。监管挑战和加快药物开发时间表的压力越来越大，使得外包对许多公司来说成为更具吸引力的选择。

市场也受益于製造技术的进步，例如连续製造流程和一次性技术，这些技术为小批量生产药物或个人化医疗提供了更灵活、更具成本效益的解决方案。仿製药和生物相似药市场的成长也大大促进了对 CDMO 服务的需求。在外包趋势不断增长、技术进步以及对具有成本效益和高品质的药品生产解决方案不断增长的需求的推动下，全球 CDMO 市场预计将持续成长。

主要市场驱动因素

对生物製剂和生物相似药的需求不断增加

製造和开发活动外包

製造技术进步

主要市场挑战

CDMO之间的激烈竞争

供应链中断

主要市场趋势

监理复杂性不断上升

新兴市场和扩大全球影响力

细分市场洞察

服务类型 CMO 见解

区域洞察

Market Overview
Forecast Period	2025-2029
Market Size 2023	USD 240.19 Billion
Market Size 2029	USD 346.69 Billion
CAGR 2024-2029	6.48%
Fastest Growing Segment	Finished Dosage Formulation (FDF) Development and Manufacturing
Largest Market	North America

The Global Contract Development and Manufacturing Organization (CDMO) Market is a rapidly growing segment within the pharmaceutical and biotechnology industries, driven by increasing demand for outsourced services related to drug development and manufacturing. CDMOs provide a wide range of services, including drug formulation, clinical trial material production, scale-up manufacturing, and commercial production. This market has expanded as pharmaceutical companies seek to reduce costs, enhance efficiency, and focus on core competencies while outsourcing non-core functions such as production and development. Key factors contributing to the market's growth include the rising complexity of drug formulations, the increasing demand for biologics and biosimilars, and the need for specialized manufacturing capabilities, particularly in the areas of sterile and high-potency drugs. Regulatory challenges and the rising pressure to expedite drug development timelines have made outsourcing a more attractive option for many companies.

The market is also benefiting from advancements in manufacturing technologies, such as continuous manufacturing processes and single-use technologies, which provide more flexible, cost-effective solutions for producing drugs in smaller batches or for personalized medicine. The growth of the generics and biosimilars markets has also contributed significantly to the demand for CDMO services. The Global CDMO Market is poised for continued growth, driven by increasing outsourcing trends, technological advancements, and the rising need for cost-effective and high-quality drug manufacturing solutions.

Key Market Drivers

Increasing Demand for Biologics and Biosimilars

The increasing demand for biologics and biosimilars is a significant driver of the Global Contract Development and Manufacturing Organization (CDMO) Market. Biologics, including monoclonal antibodies, vaccines, gene therapies, and cell-based therapies, are gaining widespread recognition for their ability to treat complex and chronic diseases such as cancer, autoimmune disorders, diabetes, and genetic conditions. These treatments often require highly specialized manufacturing processes, such as advanced bioreactor systems, precision formulation techniques, and strict sterile production environments. As the demand for biologics continues to grow, pharmaceutical companies face challenges related to the scale and complexity of production. This is where CDMOs provide essential value, offering the specialized infrastructure, technical expertise, and manufacturing flexibility needed to produce biologics on a commercial scale. For instance, In January 2024, EXO Biologics SA, a Belgian biotech company focused on developing biopharmaceuticals using exosomes to address rare diseases with significant unmet medical needs, launched ExoXpert, a contract development and manufacturing organization (CDMO) specializing in exosome production. ExoXpert, a wholly-owned subsidiary of EXO Biologics, utilizes an MSC-based exosome manufacturing platform for European clinical trials.

Biosimilars, which are cost-effective alternatives to originator biologic drugs, are rapidly gaining traction in the healthcare market. They offer a more affordable option for patients, particularly in markets where healthcare costs are rising. This shift toward biosimilars is contributing to the growth of the CDMO market, as pharmaceutical companies look to outsource their biosimilar production to take advantage of the cost efficiencies and high-quality manufacturing offered by CDMOs. With the growing need for manufacturing capacity and specialized knowledge in biologics and biosimilars, outsourcing production to CDMOs has become an increasingly popular strategy for pharmaceutical companies.

The rising demand for biologics and biosimilars is prompting pharmaceutical firms to invest in more extensive and innovative manufacturing networks. As a result, CDMOs are experiencing significant growth, benefiting from rising outsourcing trends. The expanding market for biologics and biosimilars is expected to continue driving investments into CDMO infrastructure, boosting their production capabilities and solidifying their critical role in the pharmaceutical supply chain. This ongoing trend positions the CDMO market for further expansion in the coming years.

Outsourcing of Manufacturing and Development Activities

Outsourcing of manufacturing and development activities is a critical driver of the Global Contract Development and Manufacturing Organization (CDMO) Market. Pharmaceutical and biotechnology companies are facing growing pressure to minimize operational costs, enhance production efficiency, and shorten the time-to-market for new drugs. By outsourcing drug development and manufacturing to CDMOs, companies can tap into specialized expertise, cutting-edge facilities, and flexible production capabilities, all without the substantial capital expenditure required to build and maintain their own infrastructure. This strategic shift enables companies to focus their resources on core competencies such as research and development (R&D), marketing, and sales, while relying on CDMOs to handle the complex and resource-intensive tasks of drug production.

CDMOs offer a comprehensive range of services that cover the entire lifecycle of drug development and manufacturing. This includes preclinical development, formulation development, clinical trial material production, and large-scale commercial manufacturing. By partnering with CDMOs, pharmaceutical companies can streamline their operations, enhance efficiency, and ultimately improve profitability. This outsourcing model is particularly beneficial for smaller biotechnology firms that may not have the financial resources or infrastructure to handle large-scale manufacturing in-house.

The trend of outsourcing has become even more pronounced in the wake of the COVID-19 pandemic. The global health crisis underscored the need for flexible and scalable manufacturing solutions to rapidly respond to unforeseen surges in demand for vaccines, therapeutics, and other essential medicines. CDMOs with their ability to quickly scale production were crucial in supporting the fast-tracking of vaccine development and distribution, demonstrating the strategic value of outsourcing. As drug development becomes increasingly complex with advances in biologics, gene therapies, and personalized medicine, outsourcing remains an attractive strategy for pharmaceutical companies. The demand for CDMO services is expected to continue rising, supporting the long-term growth of the CDMO market. This trend allows companies to optimize their manufacturing operations while focusing on innovation and market expansion.

Technological Advancements in Manufacturing

Technological advancements in manufacturing processes are playing a pivotal role in driving the growth of the Global Contract Development and Manufacturing Organization (CDMO) Market. The integration of state-of-the-art technologies, such as continuous manufacturing, single-use systems, and automation, has fundamentally transformed the production landscape, particularly in the pharmaceutical and biotechnology sectors. These innovations are enhancing the efficiency, scalability, and cost-effectiveness of drug manufacturing, positioning CDMOs as essential partners for pharmaceutical companies.

Continuous manufacturing is one such breakthrough that has revolutionized pharmaceutical production. This method allows for the uninterrupted, real-time production of drugs, particularly biologics, which traditionally required batch processing. By reducing downtime and minimizing the need for manual intervention, continuous manufacturing increases production efficiency and consistency. It also leads to significant reductions in waste, ensuring more sustainable and cost-effective operations. This ability to streamline production processes makes it an attractive option for pharmaceutical companies, especially in the context of biologics and complex therapies.

Single-use systems have become a key innovation in biopharmaceutical manufacturing. These disposable components offer advantages in terms of reducing the risk of cross-contamination, simplifying cleaning procedures, and lowering operational costs associated with traditional, reusable equipment. By eliminating the need for extensive cleaning and sterilization, single-use systems enhance both efficiency and safety in the production process. This flexibility is particularly beneficial for small-scale or clinical trial production, where frequent changes in production requirements are common.

In addition, automation technologies, including robotics and artificial intelligence (AI), are further optimizing manufacturing processes. These tools enable more precise and faster production, increasing overall scalability. Automated systems are also able to handle complex tasks, such as data analysis and quality control, with greater accuracy than traditional methods. As a result, CDMOs are better equipped to offer faster turnaround times, higher product quality, and more cost-effective solutions to their clients.These technological advancements are driving the demand for personalized medicine, small-batch production, and accelerated time-to-market, all of which contribute to the continued expansion of the CDMO market.

Key Market Challenges

Intense Competition Among CDMOs

The Global Contract Development and Manufacturing Organization (CDMO) Market faces significant challenges due to the intense competition among existing and new players. With the rapid growth of the pharmaceutical and biotechnology industries, the number of CDMOs has surged, leading to a highly fragmented market. Smaller, specialized CDMOs often compete with larger, well-established players that have extensive resources and global reach. This intense competition puts pressure on companies to differentiate themselves through innovation, cost-effectiveness, and the ability to offer specialized services. Smaller CDMOs may struggle to invest in cutting-edge technologies, such as continuous manufacturing and single-use systems, which are increasingly becoming industry standards. This makes it difficult for them to compete with larger companies that have the financial resources to continuously upgrade their facilities and expand their service offerings. The rise of contract manufacturers in emerging markets, which offer lower operational costs, poses a further challenge to established CDMOs in North America and Europe. To maintain a competitive edge, CDMOs must adopt advanced manufacturing technologies, maintain high-quality standards, and deliver flexibility and speed, all while managing price pressures. The challenge of staying competitive in a market that is becoming increasingly crowded can impact a CDMO's profitability and long-term sustainability.

Supply Chain Disruptions

Supply chain disruptions represent a persistent challenge for the Global CDMO Market, particularly in light of recent global events such as the COVID-19 pandemic and geopolitical tensions. The pharmaceutical and biotechnology industries rely on a complex and interconnected network of suppliers for raw materials, active pharmaceutical ingredients (APIs), packaging, and other components required for drug manufacturing. Any disruption in the supply chain can lead to delays in production, increased costs, and a shortage of critical materials. For instance, the pandemic disrupted global supply chains, leading to shortages of raw materials and delayed shipments of essential components, which impacted the ability of CDMOs to meet production deadlines. Natural disasters, transportation issues, and political instability in key manufacturing regions can further exacerbate supply chain challenges. This unpredictability forces CDMOs to diversify their supply chains, source materials from multiple regions, and implement contingency plans to mitigate risks. However, diversifying the supply chain can also increase costs and complicate logistics. CDMOs must also ensure that their suppliers adhere to strict quality and regulatory standards, further complicating supply chain management. As the demand for more complex drugs, biologics, and vaccines grows, supply chain risks are expected to intensify, and CDMOs must adopt advanced technologies such as blockchain and AI to enhance supply chain visibility and mitigate risks.

Key Market Trends

Rising Regulatory Complexity

The rising complexity of regulatory requirements in the pharmaceutical and biotechnology industries is significantly driving the demand for Contract Development and Manufacturing Organizations (CDMOs). Regulatory agencies worldwide, such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA), are implementing increasingly stringent guidelines related to drug safety, quality control, and manufacturing processes. These evolving regulations present substantial challenges for pharmaceutical companies, who must ensure compliance with a growing array of rules and standards, which often vary by region.

Meeting these regulatory demands requires substantial investments in quality management systems, regulatory affairs teams, and specialized manufacturing facilities that adhere to good manufacturing practices (GMP) and other industry standards. For many pharmaceutical companies, particularly smaller or mid-sized firms, maintaining the infrastructure and expertise required to navigate these complexities can be costly and resource-intensive. This is where CDMOs play a vital role. With their established expertise in regulatory compliance, CDMOs are equipped to manage the intricacies of local and international regulatory landscapes.

CDMOs have built strong relationships with regulatory bodies and possess the specialized knowledge necessary to guide pharmaceutical companies through the various stages of drug development and manufacturing while ensuring full compliance. This includes navigating preclinical trials, clinical trials, and commercial production-all while adhering to the required documentation, certifications, and quality controls set by regulatory agencies. As a result, pharmaceutical companies increasingly rely on CDMOs to handle the regulatory burden, allowing them to focus on their core competencies, such as innovation, research, and marketing. The growing complexity of regulatory frameworks, combined with the need for specialized expertise, has led to a surge in outsourcing manufacturing processes to CDMOs that are skilled in regulatory affairs. This trend not only enables pharmaceutical companies to ensure compliance but also accelerates their time-to-market while maintaining high standards of quality and safety.

Emerging Markets and Expanding Global Reach

Emerging markets are becoming a vital growth area for the Global Contract Development and Manufacturing Organization (CDMO) Market. Countries in regions such as Asia-Pacific, Latin America, and the Middle East are seeing rapid expansion in their pharmaceutical and biotechnology sectors. This growth is fueled by improvements in healthcare infrastructure, greater access to healthcare services, and an increasing demand for both branded and generic drugs. As these markets evolve, there is a significant rise in the need for high-quality manufacturing services that can meet local demands while ensuring compliance with international regulatory standards. CDMOs are strategically positioned to capitalize on the opportunities presented by these emerging markets. By establishing manufacturing facilities in these regions or forging partnerships with local companies, CDMOs can provide outsourced manufacturing services that support both local production needs and global supply chains. This approach allows CDMOs to enhance their global reach and meet the growing demand for pharmaceutical products in these rapidly developing economies.

In particular, countries like India and China are emerging as key hubs for contract manufacturing. According to the National Health Commission (NHC), in 2019, China had over 180 million elderly citizens living with chronic diseases, with 75 percent of them suffering from more than one condition. These nations offer competitive advantages such as relatively low labor costs, a well-established pharmaceutical industry, and access to advanced manufacturing technologies. India, with its robust generics sector, and China, with its growing biotechnology industry, are attractive locations for pharmaceutical companies looking to outsource production to high-quality yet cost-effective facilities. As a result, many pharmaceutical companies are increasingly turning to CDMOs with a strong presence in these regions to meet both local and international demand.

This expansion into emerging markets is not only driving the growth of the CDMO market but is also facilitating greater global access to life-saving medications. By leveraging the capabilities of CDMOs in emerging markets, pharmaceutical companies can meet the rising demand for affordable and high-quality drugs while optimizing their production and distribution networks. Consequently, the growing importance of emerging markets continues to be a key factor in the global expansion of the CDMO industry.

Segmental Insights

Service Type CMO Insights

Based on Service Type CMO, among the service types in the Global Contract Development and Manufacturing Organization (CDMO) Market, Finished Dosage Formulation (FDF) Development and Manufacturing is currently the dominant segment. This dominance is driven by the increasing demand for comprehensive manufacturing solutions that extend beyond just the production of active pharmaceutical ingredients (APIs) to include the entire formulation process. Finished dosage formulation involves not only the development of the drug's final form-such as tablets, capsules, injectables, or biologics-but also requires intricate expertise in drug stability, bioavailability, and proper scaling up from clinical to commercial manufacturing. As pharmaceutical companies look to outsource these complex processes, CDMOs with robust capabilities in FDF development and manufacturing offer a compelling value proposition. They provide end-to-end services, encompassing formulation development, manufacturing, packaging, and sometimes even distribution, which simplifies the supply chain for pharmaceutical companies.

The rise of biologics and personalized medicine further contributes to the growth of this segment. Biopharmaceutical companies increasingly require specialized capabilities in FDF manufacturing, as biologic drugs are typically more complex and require customized packaging and delivery systems. Regulatory compliance for these formulations is stringent, and CDMOs with expertise in navigating these regulatory challenges are in high demand.

Regional Insights

The North American region is currently the dominant market for the Global Contract Development and Manufacturing Organization (CDMO) Market. This dominance is primarily driven by the presence of a large number of established pharmaceutical and biotechnology companies in the region, coupled with substantial investments in research and development. North America is home to several leading pharmaceutical giants, including those based in the United States, which drive the demand for contract manufacturing and development services to meet the increasing need for drug production, particularly in biologics, vaccines, and specialized therapies.

The U.S. pharmaceutical market, the largest globally, continues to grow, propelled by advancements in drug development, the increasing complexity of drugs, and the rise of personalized medicine. As pharmaceutical companies look to outsource manufacturing to specialized CDMOs, North America's well-established infrastructure, skilled workforce, and regulatory expertise make it an attractive hub for CDMO operations. The region is also favored for its strong regulatory frameworks, including the U.S. Food and Drug Administration (FDA) and Health Canada, which ensures compliance with high industry standards, a key consideration for global pharmaceutical companies.

Key Market Players

Catalent Inc.
Recipharm AB
Jubilant Pharmova Limited
Thermo Fisher Scientific Inc.
Boehringer Ingelheim International GmbH
Pfizer Inc (Pfizer CentreOne)
Baxter International Inc.
Aenova Holding GmbH
Lonza Group
tesa Labtec GmbH

Report Scope:

In this report, the Global Contract Development and Manufacturing Organization Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Contract Development and Manufacturing Organization Market, By Service Type CMO:

Active Pharmaceutical Ingredient (API) Manufacturing
Finished Dosage Formulation (FDF) Development and Manufacturing
Secondary Packaging

Contract Development and Manufacturing Organization Market, By Research Phase CRO:

Pre-clinical
Phase I
Phase II
Phase III
Phase IV

Contract Development and Manufacturing Organization Market, By Region:

North America
- United States
- Canada
- Mexico
Europe
- France
- United Kingdom
- Italy
- Germany
- Spain
Asia-Pacific
- China
- India
- Japan
- Australia
- South Korea
South America
- Brazil
- Argentina
- Colombia
Middle East & Africa
- South Africa
- Saudi Arabia
- UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Contract Development and Manufacturing Organization Market.

Available Customizations:

Global Contract Development and Manufacturing Organization Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

1. Product Overview

1.1. Market Definition
1.2. Scope of the Market
- 1.2.1. Markets Covered
- 1.2.2. Years Considered for Study
- 1.2.3. Key Market Segmentations

2. Research Methodology

2.1. Objective of the Study
2.2. Baseline Methodology
2.3. Key Industry Partners
2.4. Major Association and Secondary Sources
2.5. Forecasting Methodology
2.6. Data Triangulation & Validation
2.7. Assumptions and Limitations

3. Executive Summary

3.1. Overview of the Market
3.2. Overview of Key Market Segmentations
3.3. Overview of Key Market Players
3.4. Overview of Key Regions/Countries
3.5. Overview of Market Drivers, Challenges, and Trends

4. Voice of Customer

5. Global Contract Development and Manufacturing Organization Market Outlook

5.1. Market Size & Forecast
- 5.1.1. By Value
5.2. Market Share & Forecast
- 5.2.1. By Service Type CMO (Active Pharmaceutical Ingredient (API) Manufacturing, Finished Dosage Formulation (FDF) Development and Manufacturing, Secondary Packaging)
- 5.2.2. By Research Phase CRO (Pre-clinical, Phase I, Phase II, Phase III, Phase IV)
- 5.2.3. By Company (2023)
- 5.2.4. By Region
5.3. Market Map

6. North America Contract Development and Manufacturing Organization Market Outlook

6.1. Market Size & Forecast
- 6.1.1. By Value
6.2. Market Share & Forecast
- 6.2.1. By Service Type CMO
- 6.2.2. By Research Phase CRO
- 6.2.3. By Country
6.3. North America: Country Analysis
- 6.3.1. United States Contract Development and Manufacturing Organization Market Outlook
  - 6.3.1.1. Market Size & Forecast
    - 6.3.1.1.1. By Value
  - 6.3.1.2. Market Share & Forecast
    - 6.3.1.2.1. By Service Type CMO
    - 6.3.1.2.2. By Research Phase CRO
- 6.3.2. Mexico Contract Development and Manufacturing Organization Market Outlook
  - 6.3.2.1. Market Size & Forecast
    - 6.3.2.1.1. By Value
  - 6.3.2.2. Market Share & Forecast
    - 6.3.2.2.1. By Service Type CMO
    - 6.3.2.2.2. By Research Phase CRO
- 6.3.3. Canada Contract Development and Manufacturing Organization Market Outlook
  - 6.3.3.1. Market Size & Forecast
    - 6.3.3.1.1. By Value
  - 6.3.3.2. Market Share & Forecast
    - 6.3.3.2.1. By Service Type CMO
    - 6.3.3.2.2. By Research Phase CRO

7. Europe Contract Development and Manufacturing Organization Market Outlook

7.1. Market Size & Forecast
- 7.1.1. By Value
7.2. Market Share & Forecast
- 7.2.1. By Service Type CMO
- 7.2.2. By Research Phase CRO
- 7.2.3. By Country
7.3. Europe: Country Analysis
- 7.3.1. France Contract Development and Manufacturing Organization Market Outlook
  - 7.3.1.1. Market Size & Forecast
    - 7.3.1.1.1. By Value
  - 7.3.1.2. Market Share & Forecast
    - 7.3.1.2.1. By Service Type CMO
    - 7.3.1.2.2. By Research Phase CRO
- 7.3.2. Germany Contract Development and Manufacturing Organization Market Outlook
  - 7.3.2.1. Market Size & Forecast
    - 7.3.2.1.1. By Value
  - 7.3.2.2. Market Share & Forecast
    - 7.3.2.2.1. By Service Type CMO
    - 7.3.2.2.2. By Research Phase CRO
- 7.3.3. United Kingdom Contract Development and Manufacturing Organization Market Outlook
  - 7.3.3.1. Market Size & Forecast
    - 7.3.3.1.1. By Value
  - 7.3.3.2. Market Share & Forecast
    - 7.3.3.2.1. By Service Type CMO
    - 7.3.3.2.2. By Research Phase CRO
- 7.3.4. Italy Contract Development and Manufacturing Organization Market Outlook
  - 7.3.4.1. Market Size & Forecast
    - 7.3.4.1.1. By Value
  - 7.3.4.2. Market Share & Forecast
    - 7.3.4.2.1. By Service Type CMO
    - 7.3.4.2.2. By Research Phase CRO
- 7.3.5. Spain Contract Development and Manufacturing Organization Market Outlook
  - 7.3.5.1. Market Size & Forecast
    - 7.3.5.1.1. By Value
  - 7.3.5.2. Market Share & Forecast
    - 7.3.5.2.1. By Service Type CMO
    - 7.3.5.2.2. By Research Phase CRO

8. Asia-Pacific Contract Development and Manufacturing Organization Market Outlook

8.1. Market Size & Forecast
- 8.1.1. By Value
8.2. Market Share & Forecast
- 8.2.1. By Service Type CMO
- 8.2.2. By Research Phase CRO
- 8.2.3. By Country
8.3. Asia-Pacific: Country Analysis
- 8.3.1. China Contract Development and Manufacturing Organization Market Outlook
  - 8.3.1.1. Market Size & Forecast
    - 8.3.1.1.1. By Value
  - 8.3.1.2. Market Share & Forecast
    - 8.3.1.2.1. By Service Type CMO
    - 8.3.1.2.2. By Research Phase CRO
- 8.3.2. India Contract Development and Manufacturing Organization Market Outlook
  - 8.3.2.1. Market Size & Forecast
    - 8.3.2.1.1. By Value
  - 8.3.2.2. Market Share & Forecast
    - 8.3.2.2.1. By Service Type CMO
    - 8.3.2.2.2. By Research Phase CRO
- 8.3.3. South Korea Contract Development and Manufacturing Organization Market Outlook
  - 8.3.3.1. Market Size & Forecast
    - 8.3.3.1.1. By Value
  - 8.3.3.2. Market Share & Forecast
    - 8.3.3.2.1. By Service Type CMO
    - 8.3.3.2.2. By Research Phase CRO
- 8.3.4. Japan Contract Development and Manufacturing Organization Market Outlook
  - 8.3.4.1. Market Size & Forecast
    - 8.3.4.1.1. By Value
  - 8.3.4.2. Market Share & Forecast
    - 8.3.4.2.1. By Service Type CMO
    - 8.3.4.2.2. By Research Phase CRO
- 8.3.5. Australia Contract Development and Manufacturing Organization Market Outlook
  - 8.3.5.1. Market Size & Forecast
    - 8.3.5.1.1. By Value
  - 8.3.5.2. Market Share & Forecast
    - 8.3.5.2.1. By Service Type CMO
    - 8.3.5.2.2. By Research Phase CRO

9. South America Contract Development and Manufacturing Organization Market Outlook

9.1. Market Size & Forecast
- 9.1.1. By Value
9.2. Market Share & Forecast
- 9.2.1. By Service Type CMO
- 9.2.2. By Research Phase CRO
- 9.2.3. By Country
9.3. South America: Country Analysis
- 9.3.1. Brazil Contract Development and Manufacturing Organization Market Outlook
  - 9.3.1.1. Market Size & Forecast
    - 9.3.1.1.1. By Value
  - 9.3.1.2. Market Share & Forecast
    - 9.3.1.2.1. By Service Type CMO
    - 9.3.1.2.2. By Research Phase CRO
- 9.3.2. Argentina Contract Development and Manufacturing Organization Market Outlook
  - 9.3.2.1. Market Size & Forecast
    - 9.3.2.1.1. By Value
  - 9.3.2.2. Market Share & Forecast
    - 9.3.2.2.1. By Service Type CMO
    - 9.3.2.2.2. By Research Phase CRO
- 9.3.3. Colombia Contract Development and Manufacturing Organization Market Outlook
  - 9.3.3.1. Market Size & Forecast
    - 9.3.3.1.1. By Value
  - 9.3.3.2. Market Share & Forecast
    - 9.3.3.2.1. By Service Type CMO
    - 9.3.3.2.2. By Research Phase CRO

10. Middle East and Africa Contract Development and Manufacturing Organization Market Outlook

10.1. Market Size & Forecast
- 10.1.1. By Value
10.2. Market Share & Forecast
- 10.2.1. By Service Type CMO
- 10.2.2. By Research Phase CRO
- 10.2.3. By Country
10.3. MEA: Country Analysis
- 10.3.1. South Africa Contract Development and Manufacturing Organization Market Outlook
  - 10.3.1.1. Market Size & Forecast
    - 10.3.1.1.1. By Value
  - 10.3.1.2. Market Share & Forecast
    - 10.3.1.2.1. By Service Type CMO
    - 10.3.1.2.2. By Research Phase CRO
- 10.3.2. Saudi Arabia Contract Development and Manufacturing Organization Market Outlook
  - 10.3.2.1. Market Size & Forecast
    - 10.3.2.1.1. By Value
  - 10.3.2.2. Market Share & Forecast
    - 10.3.2.2.1. By Service Type CMO
    - 10.3.2.2.2. By Research Phase CRO
- 10.3.3. UAE Contract Development and Manufacturing Organization Market Outlook
  - 10.3.3.1. Market Size & Forecast
    - 10.3.3.1.1. By Value
  - 10.3.3.2. Market Share & Forecast
    - 10.3.3.2.1. By Service Type CMO
    - 10.3.3.2.2. By Research Phase CRO

11. Market Dynamics

11.1. Drivers
11.2. Challenges

12. Market Trends & Developments

12.1. Merger & Acquisition (If Any)
12.2. Product Launches (If Any)
12.3. Recent Developments

13. Porters Five Forces Analysis

13.1. Competition in the Industry
13.2. Potential of New Entrants
13.3. Power of Suppliers
13.4. Power of Customers
13.5. Threat of Substitute Products

14. Competitive Landscape

14.1. Catalent Inc.
- 14.1.1. Business Overview
- 14.1.2. Company Snapshot
- 14.1.3. Products & Services
- 14.1.4. Financials (As Reported)
- 14.1.5. Recent Developments
- 14.1.6. Key Personnel Details
- 14.1.7. SWOT Analysis
14.2. Recipharm AB
14.3. Jubilant Pharmova Limited
14.4. Thermo Fisher Scientific Inc.
14.5. Boehringer Ingelheim International GmbH
14.6. Pfizer Inc (Pfizer CentreOne)
14.7. Baxter International Inc.
14.8. Aenova Holding GmbH
14.9. Lonza Group
14.10. tesa Labtec GmbH