Biologics Contract Development Market, with a 7.55% CAGR, is expected to grow to USD 12.758 billion in 2031 from USD 8.245 billion in 2025.
The Drugs that target the human immune system specifically are known as biologics. Vaccines, somatic cells, recombinant gene treatments, blood components, and allergic biologic goods are only a few examples of the biologics available in the market. Proteins, tissue, and nucleic acids from living beings make up biologics. These products are isolated using biotechnological techniques from sources including bacteria, animals, and humans. Since this product is extremely susceptible to contamination, pharmaceutical firms have a significant need for biologics contract development.
The increase in the number of drug development procedures, an increase in the rate of drug approval by the Food and Drug Administration, an increase in the use of targeted drug therapies, growth in the demand for personalized medicine, and an increase in the incidence of chronic diseases are major factors fueling the biologics contract development market.
In addition, the biologics contract development industry is being driven by factors such as the rising adoption of advanced technologies for biologic development, the favourable environment for clinical trials in developing nations, the surge in the number of collaborations, contracts, and mergers with local players to develop advanced biologic products, and the rising demand for the treatment of rare diseases.
Increasing incidences of various disorders in people
The prevalence of diseases including neurological disorders, gynaecological disorders, cancer, ophthalmic disorders, and cardiovascular disorders is constantly rising. For instance, according to the WHO, cancer was one of the leading causes of death worldwide and responsible for over 10 million fatalities in 2020. Healthcare CDMOs can be crucial to the treatment of patients in these situations. For the treatment of illnesses, several biopharmaceutical companies are creating cutting-edge treatments or ground-breaking solutions.
Upstream process development to show significant market growth potential
The creation of upstream processes mostly entails choosing the appropriate cell line, culture medium, bioreactor systems, and operational parameters. The majority of companies that manufacture biologics offer upstream process development services, which are highly tailored to the demands of the client's company, the limitations of applicable regulations, and the project schedule which is fueling the biologics contract development market. To thoroughly investigate the manufacturing of vaccines, medication metabolism, and cytotoxicity, the creation of artificial tissues, gene function research, the production of antibodies, and the synthesis of biological chemicals, cell lines are reportedly employed by NCBI.
Technological advancements in the biologics contract development market
CDMOs are significantly expanding the biologics contract development market share due to cutting-edge technology and specialized knowledge. In a highly competitive sector, biopharmaceutical CDMOs have the best chance of success. They are prepared to adopt cutting-edge technologies and make the required time and financial commitments to develop competitive advantages. The top CDMOs will boost capacity fast while remaining adaptable and nimble.
In response to the growing incidence of infectious illnesses and the rising need for innovative treatments, pharma, and biotech firms that need larger financial expenditures for cutting-edge technologies are collaborating with CDMOs, which is fostering the biologics contract development market share.
The North American biologics contract development market is anticipated to grow significantly.
The biologics contract development market in North America is anticipated to grow significantly. This is related to rising R&D expenditures, the local presence of multinational corporations, and those corporations' efforts to get new patents. Many biologics contract development industry expansion by various organizations is responsible for North Americaβs rising clinical trial activity. For instance, according to ClinicalTrial.Gov almost 32% of all trials completed worldwide as of July 2022, were undertaken in the United States alone. Furthermore, various studies conducted in the United States are fueling the biologics contract development market share.
Asia Pacific is also predicted to show significant growth
The biologics contract development market is anticipated to witness the greatest CAGR in Asia Pacific during the projected period. Biotechnology businesses are becoming more interested in investing in the Asia Pacific area as a result of several regulatory organization adjustments to modify clinical trial evaluation criteria following global needs. Asia Pacific nations provide potential with a vast patient pool and cutting-edge medical knowledge. The expense of doing a clinical study is quite cheap in the region when compared to Western nations.
Various companies focus on product innovation
Biologics contract development is a fast-growing industry. The competition is boosted by the advanced technology being inculcated. For the manufacture of biopharmaceuticals, CDOs are moving towards Single-Use Bioreactors (SBUs), lower batch sizes, and reduced-volume bioreactor tank sizes. Furthermore, various mergers and acquisitions in developing countries by key players in the region are fueling the market. For instance, Lonza and biotechnology business Touchlight joined in September 2022 to expand their product line with other sources of DNA for producing mRNA. Through Lonza's products, Touchlight hopes to increase the number of consumers using its innovative doggy bone DNA (dbDNA) technology.
In March 2023, for the construction of a new factory in South Korea, Samsung Biologics declared an investment of USD 1.5 billion.
In March 2023, Lonza and Simris Alg AB of Sweden collaborated to create and produce antibody-drug conjugates.
In February 2023, Lonza increased its footprint in the United States by opening a new lab devoted to creating medications that are still in the early phases of clinical testing.
WuXi Biologics
Abzena Ltd
Fujifilm Diosynth Biotechnologies
KBI Biopharma
AGC Biologics
| Report Metric | Details |
|---|---|
| Study Period | 2021 to 2031 |
| Historical Data | 2021 to 2024 |
| Base Year | 2025 |
| Forecast Period | 2026 β 2031 |
| Companies |
|
Report Metric | Details |
Biologics Contract Development Market Size in 2025 | USD 8.245 billion |
Biologics Contract Development Market Size in 2030 | USD 11.994 billion |
Growth Rate | CAGR of 7.78% |
Study Period | 2020 to 2030 |
Historical Data | 2020 to 2023 |
Base Year | 2024 |
Forecast Period | 2025 β 2030 |
Forecast Unit (Value) | USD Billion |
Segmentation |
|
Geographical Segmentation | North America, South America, Europe, Middle East and Africa, Asia Pacific |
List of Major Companies in the Biologics Contract Development Market |
|
Customization Scope | Free report customization with purchase |
Biologics Contract Development Market Segmentation
By Source
Mammalian
Non-Mammalian
By Service
Upstream Processing
Downstream Processing
Others
By Indication
Oncology
Immunological Disorders
Cardiovascular Disorders
Neurological Disorders
Others
By Application
Vaccines
Gene Therapies
Monoclonal Antibodies
Others
By Geography
North America
USA
Canada
Mexico
South America
Brazil
Argentina
Others
Europe
Germany
France
United Kingdom
Spain
Others
Middle East and Africa
Saudi Arabia
UAE
Others
Asia Pacific
China
India
Japan
South Korea
Indonesia
Thailand
Others