Report ID: SQMIG35G2185
Skyquest Technology's expert advisors have carried out comprehensive research and identified these companies as industry leaders in the Contract Research Organization Market. This Analysis is based on comprehensive primary and secondary research on the corporate strategies, financial and operational performance, product portfolio, market share and brand analysis of all the leading Contract Research Organization industry players.
The global contract research organization market is mainly fueled by the increasing demand for cost-effective options for clinical trials and drug development. Pharmaceutical and biotechnology companies are outsourcing research procedures to CROs to lower operational costs and time to market, and utilize core competencies, such as drug discovery and drug commercialization. The growing incidence of chronic disease and development of new form of therapies like biologics, cell and gene therapies is increasing the need for specialized clinical trial services.
According to SkyQuest Technology “Contract Research Organization Market By Type (Drug Discovery, Pre-Clinical), By Therapeutic Area (Oncology, Cardiology), By End-User (Pharmaceutical and Biotechnological Companies, Medical Device Companies), By Region - Industry Forecast 2025-2032,” Global Contract Research Organization Market is projected to grow at a CAGR of over 8.3% by 2032, on account of urgent need for automating quantified data. The increased complexity of clinical trials, tight regulatory approval timelines and internationalization of clinical studies have massively contributed to the growing demand for CRO expertise to manage compliance and operate multi-country trials. Advancements in technology by utilizing data management, automation, artificial intelligence, and decentralized trial solutions will demonstrate increasing efficiency of CROs and create demand for CRO partnerships to play integral roles in the drug development value chain.
|
Company |
Est. Year |
Headquarters |
Revenue |
Key Services |
|
IQVIA Holdings, Inc. |
1982 |
Melbourne, Australia |
USD 14.98 billion (2023) |
Clinical trial management, R&D solutions, regulatory affairs, real-world evidence, analytics, patient recruitment, data management |
|
LabCorp |
1969 |
Burlington, North Carolina, USA |
USD 12.16 billion (2023) |
Diagnostics, clinical laboratories, drug development support, bioanalysis, trial support |
|
Thermo Fisher Scientific (PPD business)
|
1956 |
New York, USA |
USD 42.8 billion (2024) |
Laboratory instruments, reagents, CRO services via PPD (clinical development, trial management), manufacturing |
|
ICON plc |
1990 |
Melbourne, Australia |
USD 8.12 billion (2023) |
Clinical research services, early- to late-phase clinical trials, labs, imaging, real-world intelligence, regulatory consulting |
|
Wuxi AppTec |
2000 |
Haifa, Israel |
USD 8.44 billion (2023) |
Preclinical & clinical research, discovery, testing, contract development & manufacturing (CDMO) |
|
Lonza |
1897 |
Carlsbad, California, USA |
USD 7.50 billion (2023) |
Biologics/CDMO, cell and gene therapies, drug substance and product development |
|
Syneos Health |
2018 |
Cambridge, Massachusetts, USA |
USD 5.18 billion (2023) |
Clinical development, commercialization, bioanalytical, pharmacovigilance, medical affairs |
|
Catalent, Inc. |
2007 |
San Diego, California, USA |
USD 4.28 billion (2023) |
Drug development, biologics/CDMO, delivery technologies, oral and sterile dosage manufacturing |
|
Charles River Laboratories |
1947 |
Columbia, Maryland, USA |
USD 4.13 billion (2023) |
Preclinical services, discovery, safety assessment, biologics, gene & cell therapy support |
|
Fortrea |
2023 |
Cleveland, Ohio, USA |
USD 2.67 billion (2023) |
Clinical trial services, data management, early- and late-phase trials |
IQVIA Holdings, Inc. was established in 1982 and is based in Durham, North Carolina, USA. IQVIA, which is one of the largest global CROs, was created from the merger of Quintiles and IMS Health. IQVIA provides services related to clinical trial management, data analytics, regulatory solutions and real-world evidence services.
LabCorp has its origins dating back to 1969 and has its headquarters located in Burlington, North Carolina, USA. LabCorp, with its Covance division, offers the most comprehensive portfolio of drug development and clinical laboratory services. LabCorp offers all stages of drug development, from preclinical, clinical, to post approval, and enjoys a leadership position in diagnostics and laboratory testing on a global level.
Thermo Fisher Scientific (PPD business) was founded in 1956; however, its business devoted to CRO services, PPD, was established in 1985. Headquartered in Waltham, Massachusetts, USA, Thermo Fisher is a life science organization that offers laboratory, diagnostics and CRO services through PPD. PPD provides full-service clinical trial management, data analytics, and patient recruitment solutions.
ICON plc was founded in 1990 and is headquartered in Dublin, Ireland. ICON has grown to become a leading global CRO providing a variety of services that span the entire clinical development continuum. ICON supports clinical trials from early to late phase, biometrics, imaging, labs, and real-world evidence.
WuXi AppTec was established in 2000 in Shanghai, China and has quickly grown into one of the world's largest Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO). WuXi AppTec provides a broad suite of services ranging from preclinical to clinical research, small molecule to biologics drug discovery, testing, and manufacturing support.
Lonza was established in 1897 and is based in Basel, Switzerland. The company started as a chemicals company and transformed into a global leader in the development and manufacturing of biologics, providing CRO and CDMO services that support biologics, cell, and gene therapy. Lonza is recognized in the biopharmaceutical industry for providing end-to-end solutions from early-stage development through commercial-scale manufacturing.
Syneos Health was established in 2018 because of the merger of INC Research and inVentiv Health, although the previous companies have histories into the last 2 decades. The company is based in Morrisville, North Carolina, USA, and combines clinical development expertise with commercialization services.
Catalent, Inc. was established in 2007 and is based in Somerset, New Jersey, USA. The company provides drug development, drug delivery technologies, and manufacturing services, with a strong focus on biologics. Catalent is recognized as a leading CDMO, providing support for oral, injectable, and advanced therapy products. Catalent provides support from early-stage formulation through large-scale production and provides end-to-end support for pharmaceutical companies.
Founded in 1947, Charles River Laboratories, based in Wilmington, Massachusetts, USA, is one of the oldest CROs and is especially strong in preclinical work. The company offers discovery services, safety assessment, laboratory models, and biologics support. Charles River is an important partner in early drug discovery and development, with a depth of knowledge in cell and gene therapies, among other areas.
Fortrea, incorporated as a separate CRO from Labcorp in 2023, is based in Durham, North Carolina, USA. Fortrea, as an independent CRO, focuses on clinical trial services, pharmacovigilance, and data management. Fortrea has spun off from Labcorp, but Labcorp's legacy of deep expertise in drug development makes Fortrea a strong player in the CRO space with new offerings.
The contract research organization market is expected to have ongoing growth as pharmaceutical, biotechnology, and medical device companies continue to outsource to maximize cost, improve efficiency, and speed up innovation. As R&D investment increases, the demand for advanced therapies rises, and clinical trial perform becomes more global, CROs become vital strategic partners throughout the drug development continuum. Their unique expertise, regulatory support, and technology capabilities place them at the forefront of the shifting healthcare and life sciences environment.
REQUEST FOR SAMPLE
The global CRO market is projected to grow from a CAGR of 8.3% from 2025 to 2032, due to increasing outsourcing, more clinical trials, and increased financing for medical research and drug development.
The clinical segment is the largest segment in the CRO market, continuing to grow due to an increase in the complexity of clinical trials and stringent regulatory requirements, making it the largest revenue-generating segment on a global basis.
CROs are used in therapeutic areas such as oncology, cardiology, infectious disease, neurology, immunological disorders, gastroenterology, hepatology, and others, thus supporting a vast array of pharmaceutical and biotechnology R&D.
CROs support drug discovery and preclinical research by offering specialized knowledge, saving money, and getting the work done faster; therefore allowing pharmaceutical companies to navigate the different complexities of R&D and the regulatory requirements more effectively.
North America ranks as the top region in the CRO market due to their research and development spend, operational factors of accessing clinical trials ecosystem, the presence of top pharmaceutical and biotech firms in R&D, and strong regulatory frameworks in both the U.S. and Canada.
Asia-Pacific is emerging as a developing region in CRO, due to cheaper cost of resource operations, volume of clinical trials growing, skilled labor force, and government systems in place that encourage companies, particularly China, India, and Japan.
CROs, in today’s world, provide services like clinical trials (preclinical and clinical), drug discovery services, data management, regulatory matters and pharmacovigilance to pharmaceutical biotech and medical device companies, all across the globe.
CROs can help with preclinical and clinical trials by managing every aspect, including study design, place and patient recruitment, data management, and with regulatory affairs, which means that the client has more peace of mind when they contract with a CRO to assist them in completing their research activities on time and as soon as possible, thus even faster for drug development.
Canada is becoming a more popular CRO location because of government support in R&D and the continued growth of both outsourcing and larger financing for major work, such as CAD 43 million provided by the CIHR for clinical trials looking at public health threats.
The Asia-Pacific region is becoming very popular for CRO outsourcing mainly because of low operational costs, large patient populations, and supportive regulations around the use of research in medical study. With the medical research market in the region growing, China and India are leading that growth.
Want to customize this report? This report can be personalized according to your needs. Our analysts and industry experts will work directly with you to understand your requirements and provide you with customized data in a short amount of time. We offer $1000 worth of FREE customization at the time of purchase.
Feedback From Our Clients
Report ID: SQMIG35G2185
sales@skyquestt.com
USA +1 351-333-4748