PUBLISHER: TechSci Research | PRODUCT CODE: 1732831
PUBLISHER: TechSci Research | PRODUCT CODE: 1732831
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The United States Biopharmaceuticals Contract Manufacturing Market was valued at USD 10.58 billion in 2024 and is anticipated to grow significantly, reaching USD 19.52 billion by 2030 at a CAGR of 10.72%. This growth is largely fueled by rising demand for biologics and biosimilars used to treat complex diseases through advanced therapies. Evolving manufacturing technologies-such as single-use systems and continuous processing-are improving efficiency and scalability. These innovations enable contract manufacturers to deliver cost-effective, high-quality solutions while supporting the increasing need for flexible, specialized production capabilities, especially for cell and gene therapies and personalized medicines.
Market Overview | |
---|---|
Forecast Period | 2026-2030 |
Market Size 2024 | USD 10.58 Billion |
Market Size 2030 | USD 19.52 Billion |
CAGR 2025-2030 | 10.72% |
Fastest Growing Segment | Autoimmune Diseases |
Largest Market | Mid-West |
Key Market Drivers
Rising Demand for Biologics and Biosimilars
The growing demand for biologics and biosimilars is a key factor accelerating the expansion of the United States Biopharmaceuticals Contract Manufacturing Market. Biologics, including monoclonal antibodies, recombinant proteins, vaccines, and cell and gene therapies, are vital in treating complex and chronic conditions like cancer and autoimmune disorders. These therapies offer high precision and effectiveness, making them valuable in personalized medicine. As of April 1, 2025, the FDA has licensed 69 biosimilars, with 49 launched for 17 reference molecules, reflecting their growing adoption. Additionally, the FDA's Center for Biologics Evaluation and Research reported approving 17 new biologics and 26 supplements in 2024, showcasing strong regulatory support and a thriving development pipeline.
Key Market Challenges
High Capital Investment and Operational Costs
Establishing and operating a compliant biopharmaceutical manufacturing facility in the United States involves considerable financial outlay. Building state-of-the-art infrastructure with advanced equipment, controlled environments, and stringent quality control systems leads to high initial capital expenses. Ongoing costs, including energy consumption, maintenance, skilled labor, and regulatory compliance, further intensify the financial pressure. Contract manufacturers must meet cGMP and other regulatory standards, requiring continuous investment in validation and training to avoid penalties, product recalls, or operational disruptions. These financial demands pose a major challenge, especially for organizations aiming to scale rapidly.
Key Market Trends
Adoption of Single-Use Technologies
Single-use technologies (SUTs) are increasingly being embraced in the U.S. biopharmaceutical contract manufacturing landscape for their benefits in flexibility, cost-effectiveness, and scalability. These systems-comprising disposable bioreactors, filters, and chromatography devices-help minimize contamination risks and eliminate complex cleaning requirements, thus streamlining operations. This is especially critical for CMOs handling multiple client projects and products. The growing use of SUTs reduces downtime and accelerates production timelines, which is particularly beneficial in manufacturing biologics like monoclonal antibodies, vaccines, and gene therapies where speed and compliance are essential.
In this report, the United States Biopharmaceuticals Contract Manufacturing Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
Company Profiles: Detailed analysis of the major companies present in the United States Biopharmaceuticals Contract Manufacturing Market.
United States Biopharmaceuticals Contract Manufacturing 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: