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시장보고서
상품코드
2024773
생체내 CRO 시장 보고서 : 유형별, GLP 유형별, 적응증별, 지역별(2026-2034년)In-vivo CRO Market Report by Type (Rodent, Non-Rodent), GLP Type (Non-GLP, GLP Toxicology), Indication (Autoimmune/Inflammation Conditions, Pain Management, Oncology, CNS Conditions, Diabetes, Obesity, and Others), and Region 2026-2034 |
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생체내 CRO 세계 시장 규모는 2025년에 57억 달러에 이르렀습니다. 2034년까지 시장 규모가 101억 달러에 이르고, 2026-2034년 CAGR6.49%를 나타낼 것으로 예측했습니다. 전 세계 만성질환의 유병률 증가와 제약사들의 연구개발비 증가가 시장 성장을 견인하고 있습니다.
제약사의 아웃소싱 증가
제약사들은 연구 효율성 향상과 비용 절감을 위해 in-vivo CRO(Contract Research Organization)에 아웃소싱에 집중하고 있습니다. 이들 CRO는 동물실험에 대한 전문적 지식을 제공함으로써 의약품 개발 및 규제 당국의 승인 프로세스를 가속화하는 동시에 각 회사가 핵심 사업에 집중할 수 있도록 돕고 있습니다. 예를 들어, 2024년 7월, 데이터 기반 상업화를 위한 종합적인 데이터, 컨설팅, 기술, 아웃소싱 플랫폼을 제공하는 IntegriChain은 보다 수익성 높은 의약품 상업화 전략을 수립하기 위해 선도적인 제약 자문 및 매니지드 서비스 기업인 Federal Compliance Solutions(FCS)를 인수했습니다. 생체내 CRO 시장 분석 보고서에 따르면, 이것이 성장을 가속하는 요인으로 작용하고 있습니다.
전문화된 CRO 서비스의 부상
전문화된 생체 내 CRO 서비스의 부상은 전임상시험의 틈새 전문 지식에 대한 수요 증가를 반영하고 있습니다. 이들 CRO는 동물모델, 약동학, 독성학 등의 분야에서 맞춤형 서비스를 제공함으로써 치료제 연구개발의 효율성과 정확성을 향상시키고, 생체내 CRO 시장 수요를 확대되고 있습니다. 예를 들어, 2024년 6월 린더스 헬스는 생체 내 CRO 전문성과 첨단 기술, 피험자 모집 전략을 결합한 올인원 의료기기 CRO 서비스를 시작했습니다. 이를 통해 의료기기 임상시험의 효율성을 높이고, 다양한 치료 영역과 규제 경로에서 피험자 등록을 가속화할 수 있게 되었습니다.
의약품 개발에 대한 관심 증가
의약품 개발에 대한 관심이 높아지면서 생체내 CRO에 대한 지원도 확대되고 있습니다. 이들 기관은 전임상시험에 필수적인 서비스를 제공하여 제약회사가 생체 내에서 신약의 안전성과 유효성을 평가할 수 있도록 함으로써 개발 프로세스를 가속화하고 비용과 자원을 절감할 수 있도록 돕습니다. 예를 들어, 2024년 5월에는 카나비노이드 계열 의약품 임상시험을 전문으로 하는 CRO인 Cannovation Clinical Research Partners가 설립되었습니다. 회사는 전임상 및 임상 단계에 중점을 두고 제약사, 대학, DEA(미국 마약단속국) 연구진과의 협업을 통해 카나비노이드 계열 치료제를 개발하고 있습니다.
The global in-vivo CRO market size reached USD 5.7 Billion in 2025. Looking forward, IMARC Group expects the market to reach USD 10.1 Billion by 2034, exhibiting a growth rate (CAGR) of 6.49% during 2026-2034. The growing prevalence of chronic diseases worldwide and the increasing R&D expenditure by pharmaceutical companies are propelling the market growth.
Increased Outsourcing by Pharmaceutical Companies
Pharmaceutical companies are focusing on outsourcing to in-vivo contract research organizations to enhance research efficiency and reduce costs. These CROs provide specialized expertise in animal studies, thereby enabling faster drug development and regulatory approval while allowing companies to focus on core competencies. For example, in July 2024, IntegriChain, delivering pharma's comprehensive data, consulting, technology, and outsourcing platform for data-driven commercialization, acquired Federal Compliance Solutions (FCS), a leading pharma advisory and managed services firm, to develop more profitable drug commercialization strategies. According to the in-vivo CRO market analysis report, this is acting as a growth-inducing factor.
Rise of Specialized CRO Services
The rise of specialized in-vivo CRO services reflects a growing demand for niche expertise in preclinical studies. These CROs offer tailored services in areas like animal modeling, pharmacokinetics, and toxicology, enhancing drug development efficiency and precision in therapeutic research and development, escalating the in-vivo CRO market demand. For instance, in June 2024, Lindus Health launched an all-in-one medical device CRO service, combining in-vivo CRO expertise with advanced technology and recruitment strategies, streamlining medical device clinical trials, accelerating participant enrollment across various therapeutic areas and regulatory pathways, etc.
Growing Focus on Drug Development
The increasing emphasis on drug development has led to greater support for in-vivo CRO. These organizations provide essential services for preclinical testing, enabling pharmaceutical companies to evaluate the safety and efficacy of new drugs in living organisms, speeding up the development process while reducing costs and resource requirements. For example, in May 2024, Cannovation Clinical Research Partners launched as a CRO specializing in cannabis-based drug trials, focusing on preclinical and clinical phases, developed cannabinoid-based therapeutics through collaborations with pharmaceutical companies, universities, and DEA researchers.
Rodent dominates the in-vivo CRO market share
Rodents, particularly mice and rats, dominate the market due to their genetic similarity to humans, cost-effectiveness, and rapid breeding. For example, mice are extensively used for cancer research and drug testing in preclinical trials. Moreover, companies, such as Envigo and Charles River Laboratories, developed advanced rodent models and enhanced services to support several stages of drug development.
GLP toxicology exhibits a clear dominance in the market
According to the in-vivo CRO market forecast report, GLP toxicology dominates the market, as companies strive to meet the growing demand for rigorous safety assessment in drug development. Advanced GLP toxicology services, including innovative study designs, specialized toxicology models, and enhanced data analytics platforms by leading organizations, like Covance and Labcorp Drug Development, are gaining traction.
Oncology dominates the in-vivo CRO market outlook
Oncology dominates the market due to the high demand for cancer drug research and development. For example, CROs conduct animal studies to evaluate the efficacy and safety of new oncology therapies before clinical trials. Besides this, the rising innovations in supporting biotech and pharmaceutical companies to develop new cancer therapies are driving the segment's growth.
North America dominates the market
The report has also provided a comprehensive analysis of all the major regional markets, which include North America (the United States and Canada); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Latin America (Brazil, Mexico, and others); and the Middle East and Africa. According to the report, North America accounted for the largest market share.
According to the in-vivo CRO market outlook report, North America leads the market due to its advanced healthcare infrastructure, substantial R&D investment, and presence of major pharmaceutical companies. The region benefits from a strong regulatory framework, experienced researchers, and high clinical trial activity. For instance, Charles River Laboratories, a key player in the U.S., provides comprehensive in-vivo services, from early-stage research to preclinical testing, which attracts global clients seeking high-quality, reliable research outcomes. This advantage positions North America as a dominant region.