Global In Vivo Contract Research Organizations (CROs) Market Growth, Share, Size, Trends and Forecast (2024 - 2030)
By Product type;
Rodent based and Non rodent based.By Applications ;
Autoimmune, Pain Management, Oncology, CNS Conditions, Diabetes, Obesity and Others.By Geography;
North America, Europe, Asia Pacific, Middle East and Africa and Latin America - Report Timeline (2020 - 2030).Introduction
Global In Vivo Contract Research Organizations (CROs) Market (USD Million), 2020 - 2030
In the year 2023, the Global In Vivo Contract Research Organizations (CROs) Market was valued at USD 3,510.80 million. The size of this market is expected to increase to USD 5,862.62 million by the year 2030, while growing at a Compounded Annual Growth Rate (CAGR) of 7.6%.
In-vivo contract research organizations (IV-CROs) are gaining prominence within the biopharmaceutical research landscape. These specialized CROs focus on conducting research in vivo, meaning they perform experiments within living organisms. As biologics, such as monoclonal antibodies (mABs), gain traction over traditional small molecule drugs, the demand for IV-CROs is on the rise. This shift underscores the industry's evolving needs, with a growing emphasis on exploring biologics' therapeutic potential and addressing complex disease targets.
The surge in interest towards biologics has propelled IV-CROs to center their efforts on biosimilar development. Biosimilars, which are highly similar versions of already-approved biologic medicines, offer a lucrative opportunity in a competitive landscape. With the development focus veering towards bispecifics or biosimilars, IV-CROs are strategically positioning themselves to cater to the evolving demands of the biopharmaceutical market. This strategic shift reflects the industry's quest for innovation and cost-effective solutions in drug development.
As the demand for clinical-scale manufacturing of active pharmaceutical components intensifies, integrated contract research, development, and manufacturing organizations (CDMOs) are expanding their footprint across various sectors. By offering end-to-end services encompassing research, development, and manufacturing capabilities, these integrated CDMOs provide a comprehensive solution to biopharmaceutical companies. This trend signifies the industry's inclination towards streamlining operations and consolidating services under a single entity, thus optimizing efficiency and facilitating seamless transitions from research to commercialization.
Global In Vivo Contract Research Organizations (CROs) Market Report Snapshot
Parameters | Description |
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Market | Global In Vivo Contract Research Organizations (CROs) Market |
Study Period | 2020 - 2030 |
Base Year (for In Vivo Contract Research Organizations (CROs) Market Size Estimates) | 2023 |
Drivers |
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Restraints |
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Opportunities |
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Segment Analysis
The global market for in vivo contract research organizations (CROs) can be segmented based on various factors such as the type of services offered, therapeutic area focus, and geographic regions. In terms of services, IV-CROs typically provide a wide range of preclinical and nonclinical research services, including pharmacokinetics, toxicology studies, efficacy testing, and safety assessments. These services cater to the needs of biopharmaceutical companies and research institutions seeking expertise and resources to conduct in vivo experiments in compliance with regulatory requirements. IV-CROs often specialize in specific areas such as oncology, immunology, neuroscience, or metabolic disorders, allowing them to deliver specialized services tailored to the unique requirements of different therapeutic areas.
The global market for in vivo CROs spans regions such as North America, Europe, Asia Pacific, Latin America, and the Middle East & Africa. North America and Europe account for a significant share of the market, driven by established biopharmaceutical industries, advanced research infrastructure, and stringent regulatory frameworks. These regions are home to numerous IV-CROs offering a diverse range of services to support drug discovery and development programs. In contrast, the Asia Pacific region is experiencing rapid growth in the IV-CRO market, fueled by increasing investments in biomedical research, outsourcing trends, and a growing focus on biosimilar development. Emerging economies in Asia Pacific, such as China and India, are becoming attractive destinations for outsourcing preclinical research activities due to cost advantages and a skilled workforce.
Global In Vivo Contract Research Organizations (CROs) Segment Analysis
In this report, the Global In Vivo Contract Research Organizations (CROs) Market has been segmented by Product type, Applications and Geography.
Global In Vivo Contract Research Organizations (CROs) Market, Segmentation by Product Type
The Global In Vivo Contract Research Organizations (CROs) Market has been segmented by Product type into Rodent based and Non rodent based.
The rodent-based studies involve the use of mice, rats, and other rodents as experimental models for conducting preclinical research. These models are widely employed in various fields of biomedical research, including pharmacology, toxicology, and disease modeling, owing to their physiological similarities to humans and well-established genetic tools. In vivo CROs specializing in rodent-based research offer a range of services, such as safety assessments, efficacy studies, and pharmacokinetic evaluations, using rodent models to test the safety and efficacy of pharmaceutical compounds and biologics.
On the other hand, non-rodent-based research services utilize alternative animal models, such as rabbits, guinea pigs, dogs, non-human primates, and various other species, to conduct preclinical studies. Non-rodent models offer distinct advantages, such as larger body size, closer resemblance to human physiology in certain aspects, and relevance to specific disease conditions. In vivo CROs specializing in non-rodent-based research cater to the diverse needs of biopharmaceutical companies and research institutions, offering customized study designs and experimental protocols tailored to the unique requirements of different therapeutic areas and drug development programs.
The choice between rodent-based and non-rodent-based research models depends on various factors, including the research objectives, target species, regulatory requirements, and ethical considerations. While rodent models are commonly used due to their availability, cost-effectiveness, and ease of handling, non-rodent models are preferred for certain studies requiring larger animal sizes, specialized physiological features, or specific disease models. In vivo CROs play a pivotal role in providing access to a wide range of research models, expertise, and resources to support drug discovery and development efforts, helping biopharmaceutical companies navigate the complexities of preclinical research and accelerate the translation of promising therapies from bench to bedside.
Global In Vivo Contract Research Organizations (CROs) Market, Segmentation by Applications
The Global In Vivo Contract Research Organizations (CROs) Market has been segmented by Applications into Autoimmune, Pain Management, Oncology, CNS Conditions, Diabetes, Obesity and Others.
The diverse needs of biopharmaceutical companies and research institutions. One significant segment is oncology, which encompasses research related to the prevention, diagnosis, and treatment of cancer. In vivo CROs specializing in oncology conduct preclinical studies to evaluate the safety and efficacy of potential cancer therapies, including novel drug candidates, targeted therapies, and immunotherapies. These studies play a crucial role in advancing oncology research and development, guiding clinical trial design, and ultimately improving patient outcomes.
Another important application segment is autoimmune diseases, which involve conditions where the body's immune system mistakenly attacks its own tissues. In vivo CROs focusing on autoimmune research conduct preclinical studies to investigate the underlying mechanisms of autoimmune diseases and evaluate potential therapeutic interventions. These studies may involve animal models designed to mimic specific autoimmune conditions, such as rheumatoid arthritis, multiple sclerosis, or lupus. By providing insights into disease pathogenesis and therapeutic targets, in vivo CROs contribute to the development of innovative treatments for autoimmune disorders.
In vivo CROs play a crucial role in preclinical research related to central nervous system (CNS) conditions, including neurodegenerative diseases, psychiatric disorders, and neurological disorders. CNS research encompasses a wide range of conditions such as Alzheimer's disease, Parkinson's disease, depression, anxiety disorders, and epilepsy. In vivo CROs specializing in CNS research conduct preclinical studies to evaluate the safety and efficacy of potential CNS therapies, assess drug pharmacokinetics and pharmacodynamics, and investigate disease mechanisms. These studies are essential for advancing our understanding of CNS disorders and developing new treatments to address unmet medical needs in this therapeutic area.
Global In Vivo Contract Research Organizations (CROs) Market, Segmentation by Geography
In this report, the Global In Vivo Contract Research Organizations (CROs) Market has been segmented by Geography into five regions; North America, Europe, Asia Pacific, Middle East and Africa and Latin America.
Global In Vivo Contract Research Organizations (CROs) Market Share (%), by Geographical Region, 2023
North America and Europe stand out as mature markets for in vivo CROs, driven by advanced healthcare infrastructure, robust pharmaceutical and biotechnology industries, and stringent regulatory frameworks. These regions host numerous IV-CROs offering a wide range of preclinical research services, including pharmacokinetics, toxicology studies, and efficacy testing. Additionally, the presence of leading biopharmaceutical companies and academic research institutions in North America and Europe contributes to the demand for specialized in vivo research expertise and resources.
In contrast, the Asia Pacific region is witnessing rapid growth in the in vivo CRO market, propelled by increasing investments in biomedical research, outsourcing trends, and a growing focus on biosimilar development. Countries like China, India, and South Korea are emerging as attractive destinations for outsourcing preclinical research activities due to their cost advantages, skilled workforce, and supportive regulatory environment. Moreover, the Asia Pacific region offers access to diverse patient populations, facilitating the conduct of clinical trials and translational research studies. As a result, both domestic and international IV-CROs are expanding their presence in Asia Pacific to capitalize on these opportunities and cater to the evolving needs of biopharmaceutical companies.
Latin America and the Middle East & Africa regions also present growth opportunities for in vivo CROs, driven by increasing investments in healthcare infrastructure, rising prevalence of chronic diseases, and expanding pharmaceutical markets. While these regions may face challenges such as regulatory complexities and infrastructure limitations, there is a growing recognition of the importance of preclinical research in drug discovery and development. IV-CROs operating in Latin America and the Middle East & Africa often collaborate with local research institutions and government agencies to address healthcare needs and accelerate medical innovation. Overall, the segmentation of the global in vivo CRO market by geography reflects the evolving dynamics of the pharmaceutical industry and the increasing globalization of research and development activities.
Market Trends
This report provides an in depth analysis of various factors that impact the dynamics of Global In Vivo Contract Research Organizations (CROs) Market. These factors include; Market Drivers, Restraints and Opportunities Analysis.
Drivers, Restraints and Opportunity Analysis
Drivers
- Biopharmaceutical Research
- In Vivo Studies
- Biologics
-
Monoclonal Antibodies (mABs): Monoclonal antibodies (mABs) represent a significant area of focus within the Global In Vivo Contract Research Organizations (CROs) Market. As biologic therapeutics, mABs have garnered considerable attention in drug development due to their specificity, efficacy, and potential for targeted therapy across various disease indications. In vivo CROs play a crucial role in supporting the preclinical development of mABs, conducting studies to evaluate their pharmacokinetics, pharmacodynamics, safety profiles, and efficacy in animal models. These studies are essential for gaining insights into mABs' therapeutic potential, optimizing dosing regimens, and informing subsequent clinical trial designs.
In response to the growing demand for mABs in the pharmaceutical industry, in vivo CROs are increasingly specializing in supporting mAB development programs. These specialized CROs offer a comprehensive range of services tailored to the unique requirements of mAB research, including hybridoma generation, antibody production, in vivo efficacy studies, pharmacokinetic assessments, and immunogenicity testing. By leveraging their expertise and infrastructure, in vivo CROs enable biopharmaceutical companies to expedite the preclinical development of mAB candidates, mitigate risks, and make informed decisions regarding their advancement into clinical trials.
As the pipeline's focus shifts towards next-generation mABs, such as bispecific antibodies and antibody-drug conjugates (ADCs), in vivo CROs are adapting their capabilities and offerings to accommodate these evolving needs. Bispecific antibodies, which can simultaneously target two different antigens or pathways, hold promise for treating complex diseases and overcoming treatment resistance. In vivo CROs play a critical role in assessing the pharmacokinetics, target engagement, and therapeutic efficacy of bispecific antibodies in preclinical models, facilitating their translation into clinical development. Similarly, in vivo CROs are well-positioned to support the preclinical evaluation of ADCs, which combine the specificity of mABs with the cytotoxic properties of small molecule drugs, offering targeted and potent anticancer therapies. Overall, the segment focused on mABs underscores the integral role of in vivo CROs in advancing biologic therapeutics and driving innovation in drug discovery and development.
Restraints
- Regulatory Challenges
- Cost Constraints
- Ethical Concerns
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Limited Expertise: The Global In Vivo Contract Research Organizations (CROs) Market faces significant challenges stemming from limited expertise in specialized areas of research and development. While in vivo CROs offer a broad spectrum of preclinical research services, including pharmacokinetics, toxicology studies, and efficacy testing, they often encounter difficulties in addressing niche therapeutic domains or emerging scientific methodologies. Conducting research on rare diseases or specialized indications demands specific knowledge and experience, which may not be readily available within every IV-CRO. Consequently, biopharmaceutical companies seeking support for complex research endeavors may confront obstacles in finding IV-CROs equipped with the necessary expertise to fulfill their requirements adequately.
The swift pace of technological advancement in biomedical research poses a formidable challenge for in vivo CROs to keep abreast of evolving scientific methodologies and tools. Emerging technologies like gene editing, CRISPR-Cas9, and organ-on-a-chip models are reshaping the landscape of preclinical research, offering novel avenues for understanding disease mechanisms and drug development. However, the adoption and incorporation of these advanced technologies into IV-CRO services necessitate specialized training, infrastructure, and resources. IV-CROs that fail to invest in staying abreast of technological innovations risk falling behind, compromising their competitiveness and ability to meet the evolving demands of biopharmaceutical clients.
The global in vivo CRO market grapples with talent shortages and intense competition for skilled professionals, particularly in regions with limited access to specialized training programs or research facilities. Recruiting and retaining qualified scientists, veterinarians, and technical staff proficient in in vivo research methodologies present ongoing challenges for IV-CROs. The shortage of experienced professionals in specific therapeutic domains or research disciplines further impedes IV-CROs' capacity to expand their service offerings and cater effectively to the diverse needs of biopharmaceutical clients.
Opportunities
- Biologics
- Biosimilar development
- Monoclonal antibodies (mABs)
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Bispecifics: Bispecific antibodies represent a growing area of interest within the Global In Vivo Contract Research Organizations (CROs) Market. Bispecific antibodies are engineered molecules that can simultaneously target two different antigens, offering unique therapeutic advantages in treating various diseases, including cancer, autoimmune disorders, and infectious diseases. As the development of bispecific antibodies gains momentum in the biopharmaceutical industry, in vivo CROs are increasingly called upon to provide specialized expertise and services for preclinical evaluation and validation of these novel therapeutics.
In vivo CROs play a crucial role in supporting bispecific antibody development through a range of preclinical research services, including pharmacokinetic studies, safety assessments, and efficacy testing in relevant disease models. These CROs leverage their expertise in in vivo research methodologies, animal models, and regulatory compliance to conduct comprehensive evaluations of bispecific antibodies, helping biopharmaceutical companies assess their pharmacological properties, safety profiles, and therapeutic potential. Moreover, in vivo CROs may offer customized study designs and specialized models to address the unique challenges associated with bispecific antibody development, such as target specificity, pharmacokinetics, and immunogenicity.
The demand for in vivo CRO services in the field of bispecific antibodies is driven by the increasing complexity and diversity of these therapeutics, as well as the growing competition among biopharmaceutical companies to bring innovative products to market. As bispecific antibody pipelines expand and diversify, in vivo CROs are expected to play an integral role in supporting preclinical development programs, facilitating the translation of promising candidates from early-stage research to clinical trials. By providing high-quality, scientifically rigorous preclinical data, in vivo CROs contribute to the de-risking of bispecific antibody candidates and the optimization of therapeutic strategies, ultimately advancing the field of biopharmaceutical innovation.
Competitive Landscape Analysis
Key players in Global In Vivo Contract Research Organizations (CROs) Market include:
- PPD Inc. (U.S)
- Quintiles (U.S)
- ICON Plc (Ireland)
- Parexel International Corporation (U.S)
- American Preclinical Services
- LLC (U.S)
- Labcorp Drug Development (U.S)
- Theorem Clinical research (U.S)
- WuXi AppTec (China)
- Syneos Health (U.S)
- Evotec (Germany)
- Charles River Laboratories (U.S)
In this report, the profile of each market player provides following information:
- Company Overview
- Key Developments
- Financial Overview
- Strategies
- Company SWOT Analysis
- Introduction
- Research Objectives and Assumptions
- Research Methodology
- Abbreviations
- Market Definition & Study Scope
- Executive Summary
- Market Snapshot, By Product Type
- Market Snapshot, By Applications
- Market Snapshot, By Region
- Global In Vivo Contract Research Organizations (CROs) Market Dynamics
- Drivers, Restraints and Opportunities
- Drivers
- Biopharmaceutical Research
- In Vivo Studies
- Biologics
- Monoclonal Antibodies (mABs)
- Restraints
- Regulatory Challenges
- Cost Constraints
- Ethical Concerns
- Limited Expertise
- Opportunities
- Biologics
- Biosimilar development
- Monoclonal antibodies (mABs)
- Bispecifics
- Drivers
- PEST Analysis
- Political Analysis
- Economic Analysis
- Social Analysis
- Technological Analysis
- Porter's Analysis
- Bargaining Power of Suppliers
- Bargaining Power of Buyers
- Threat of Substitutes
- Threat of New Entrants
- Competitive Rivalry
- Drivers, Restraints and Opportunities
- Market Segmentation
- Global In Vivo Contract Research Organizations (CROs) Market, By Product Type, 2020 - 2030 (USD Million)
- Rodent based
- Non rodent based
- Global In Vivo Contract Research Organizations (CROs) Market, By Applications, 2020 - 2030 (USD Million)
- Autoimmune
- Pain Management
- Oncology
- CNS Conditions
- Diabetes
- Obesity
- Others
- Global In Vivo Contract Research Organizations (CROs) Market, By Geography, 2020 - 2030 (USD Million)
- North America
- United States
- Canada
- Europe
- Germany
- United Kingdom
- France
- Italy
- Spain
- Nordic
- Benelux
- Rest of Europe
- Asia Pacific
- Japan
- China
- India
- Australia/New Zealand
- South Korea
- ASEAN
- Rest of Asia Pacific
- Middle East & Africa
- GCC
- Israel
- South Africa
- Rest of Middle East & Africa
- Latin America
- Brazil
- Mexico
- Argentina
- Rest of Latin America
- North America
- Global In Vivo Contract Research Organizations (CROs) Market, By Product Type, 2020 - 2030 (USD Million)
- Competitive Landscape
- Company Profiles
- PPD Inc. (U.S)
- Quintiles (U.S)
- ICON Plc (Ireland)
- Parexel International Corporation (U.S)
- American Preclinical Services
- LLC (U.S)
- Labcorp Drug Development (U.S)
- Theorem Clinical research (U.S)
- WuXi AppTec (China)
- Syneos Health (U.S)
- Evotec (Germany)
- Charles River Laboratories (U.S)
- Company Profiles
- Analyst Views
- Future Outlook of the Market
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