The Biologics Contract Development and Manufacturing Organization (CDMO) sector is currently experiencing growth in its life cycle. This growth is marked by a rising acceptance of biologics, an increasing need for outsourced manufacturing services, and a growing investment in expanding CDMO capacity.
The global biologics CDMO market is projected to reach $80.05 billion by 2032 from $19.00 billion in 2022, growing at a CAGR of 15.43% during the forecast period 2022-2032.
The market’s direction indicates a profound influence on pharmaceutical care. Companies that skillfully navigate regulatory challenges and embrace technological advancements are positioned for substantial success in this transformative landscape.
Market Analysis: Trends, Data, and Growth Projections
BIS Research, a leading market research firm, has released a report titled Biologics CDMO Market which discusses the challenges, growth factors, and future opportunities driving the remarkable market growth.
The Biologics CDMO Market report focuses on several segments such as cell type, indication, molecule type, region, etc.
China dominated the Asia-Pacific market in 2022 with a share of 40.18%. Moreover, by molecule type the market was dominated by the monoclonal antibodies segment.
Key Players and Market Shares
Having a worldwide presence, these Contract Development and Manufacturing Organizations (CDMOs) are strategically positioned to meet the growing industry demand for flexible, high-quality, and efficient solutions in the development and manufacturing of biologics.
Some major companies operating in the Biologics CDMO Market are:
- AbbVie Inc.
- AGC Biologics
- Binex Co. Limited
- Boehringer Ingelheim International GmbH
- Catalent, Inc
- Lonza
- Novartis AG
- Parexel International Corporation
- Samsung Biologics
- Toyobo Co., Ltd.
Market Drivers, Challenges, and Opportunities
Regulatory advancements, ongoing research, and collaboration between industry leaders are contributing factors in the growth of the Biologics CDMO Market.
Market Drivers:
- Growing Biologics Approvals and Development
- Rising Prevalence of Chronic Infectious Diseases
- Advantages of Investment in Contract Manufacturing Facilities
Market Restraints:
- Stringent Regulatory Requirements
- Shortage of Skilled Professionals in Bioprocessing and Biomanufacturing
Market Opportunities:
- New Outsourcing Opportunities in China
- Potential for Additional CDMO and Big Pharma Alliances
Related Reports
Nucleic Acid Therapeutics CDMO Market
Analyst Note
BIS principal analyst suggests: “The global biologics CDMO market is experiencing significant growth driven by a confluence of factors. One of the primary drivers is the growing number of biologics approvals and developments, as the surge in approvals reflects the growing significance of biopharmaceuticals in treating various medical conditions and the expanding pipeline of innovative biologic drugs.”
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Our strategic market analysis emphasizes market estimations, technology analysis, emerging high-growth applications, deeply segmented granular country-level market data, and other important market parameters useful in the strategic decision-making for senior management.
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