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시장보고서
상품코드
1714525
임상시험 용품 시장 : 세계 산업 규모, 점유율, 동향, 기회, 예측 - 임상 단계별, 제품 및 서비스별, 치료 용도별, 최종사용자별, 지역별, 경쟁별(2020-2030년)Clinical Trial Supplies Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Clinical Phase, By Product & Services, By Therapeutic Use, By End User, By Region and Competition, 2020-2030F |
임상시험 용품 세계 시장 규모는 2024년 28억 1,000만 달러로 2030년까지 7.43%의 CAGR로 2030년에는 43억 3,000만 달러에 달할 것으로 예상됩니다.
전 세계적으로 임상시험의 양과 복잡성이 증가함에 따라 임상시험 시장은 지속적으로 성장하고 있습니다. 제약 및 바이오 제약 기업들이 새로운 치료법 개발을 가속화함에 따라 합리적이고 신뢰할 수 있으며 컴플라이언스를 준수하는 공급망에 대한 수요가 증가하고 있습니다. 임상시험은 지리적으로 분산되어 있고, 기간이 길어지고 있으며, 규제 요건이 더욱 엄격해지고 있습니다. 이에 따라 효율적인 물류, 온도 관리 보관, 실시간 추적 시스템에 대한 필요성이 증가하고 있습니다. 적응성 높은 임상시험 설계와 맞춤형 의료의 채택은 공급 프로세스를 더욱 복잡하게 만들고 있으며, 스폰서들은 유연하고 확장 가능한 공급 파트너를 찾고 있습니다.
시장 개요 | |
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예측 기간 | 2026-2030년 |
시장 규모 : 2024년 | 28억 1,000만 달러 |
시장 규모 : 2030년 | 43억 3,000만 달러 |
CAGR : 2025-2030년 | 7.43% |
급성장 부문 | 심혈관질환 |
최대 시장 | 북미 |
임상시험 물류 시장의 핵심 트렌드는 임상시험 물류에 디지털 기술이 통합되고 있다는 점입니다. 분산형 및 하이브리드 임상시험 모델의 부상으로 임상시험 의뢰자와 임상시험수탁기관(CRO)은 DTP(Direct to Patient) 공급 전략을 채택하고 모니터링, 예측, 재고 관리를 위해 디지털 도구를 채택하고 있습니다. 수요 계획 및 데이터 분석을 위한 첨단 소프트웨어 플랫폼의 도입은 낭비를 줄이고, 정확성을 높이며, 실시간 의사결정을 내리는 데 도움이 되고 있습니다. 스마트 포장, 데이터 보안을 위한 블록체인, AI 기반 예측과 같은 혁신은 업무 효율성 향상과 규제 준수를 보장하기 위해 활용되고 있습니다.
치료 영역 전반에 걸친 임상시험 수 증가
세계 공급망 관리의 복잡성
공급망 디지털화 및 실시간 모니터링 채택 증가
The Global Clinical Trial Supplies Market was valued at USD 2.81 billion in 2024 and is expected to reach USD 4.33 billion by 2030, growing at a CAGR of 7.43% through 2030. The market is experiencing sustained growth due to the increasing volume and complexity of clinical trials globally. As pharmaceutical and biopharmaceutical companies aim to accelerate the development of new therapies, the demand for streamlined, reliable, and compliant supply chains has intensified. Clinical trials are becoming more geographically dispersed, longer in duration, and subject to stricter regulatory requirements. This increases the need for efficient logistics, temperature-controlled storage, and real-time tracking systems. The adoption of adaptive trial designs and personalized medicine is further complicating the supply process, prompting sponsors to seek supply partners with flexible and scalable capabilities.
Market Overview | |
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Forecast Period | 2026-2030 |
Market Size 2024 | USD 2.81 Billion |
Market Size 2030 | USD 4.33 Billion |
CAGR 2025-2030 | 7.43% |
Fastest Growing Segment | Cardiovascular Diseases |
Largest Market | North America |
A significant trend shaping the market is the integration of digital technologies in clinical trial logistics. The rise of decentralized and hybrid trial models is pushing sponsors and contract research organizations (CROs) to adopt direct-to-patient (DTP) supply strategies and employ digital tools for monitoring, forecasting, and inventory control. The implementation of advanced software platforms for demand planning and data analytics is helping reduce waste, improve accuracy, and support real-time decision-making. Innovations like smart packaging, blockchain for data security, and AI-driven forecasting are being leveraged to enhance operational efficiency and ensure regulatory compliance.
Key Market Drivers
Rising Number of Clinical Trials Across Therapeutic Areas
The increasing number of clinical trials across various therapeutic areas is a key driver for the Global Clinical Trial Supplies Market. Pharmaceutical, biotechnology, and medical device companies are expanding their research and development pipelines, leading to a surge in clinical research activities. This growth is fueled by increased investments in drug discovery and innovation, along with the growing prevalence of chronic diseases such as cancer, diabetes, cardiovascular disorders, and autoimmune conditions. As new molecules and biologics enter the clinical stage, the demand for efficient and reliable supply chains becomes critical. Sponsors require specialized logistics and packaging services to support complex trial protocols, manage temperature-sensitive products, and ensure the timely delivery of investigational medicinal products (IMPs) to global trial sites.
According to the World Health Organization's International Clinical Trials Registry Platform (ICTRP), the number of newly recruiting trials has steadily increased, with significant growth in regions such as South-East Asia, especially in India. This upward trend in clinical trial activity necessitates robust clinical trial supply chains to handle the increasing complexity and volume of trials. The rise of decentralized trials and direct-to-patient models has further emphasized the need for innovative supply strategies and cold chain infrastructure.
Key Market Challenges
Complexity in Managing Global Supply Chains
Managing global supply chains in the clinical trial supplies market presents significant logistical challenges. Clinical trials are increasingly conducted across multiple countries, complicating supply chain coordination due to varying timelines, different customs regulations, local language requirements, and multiple vendor engagements. Fluctuations in demand forecasts, unpredictable patient enrollment, and protocol amendments further strain supply planning and inventory management. Maintaining drug stability, ensuring timely delivery of investigational products, and preventing stockouts or wastage require highly responsive and adaptive systems. Specialized cold chain logistics and real-time monitoring become even more critical for temperature-sensitive drugs and biologics. As trials move toward decentralized models with direct-to-patient delivery and remote participation, the supply chain must evolve to remain flexible while maintaining quality and compliance. These challenges often add significant costs to trial budgets.
Key Market Trends
Increased Adoption of Supply Chain Digitalization and Real-Time Monitoring
The adoption of supply chain digitalization and real-time monitoring is transforming the operational landscape of the global clinical trial supplies market. Pharmaceutical sponsors and contract research organizations are prioritizing end-to-end visibility to manage the growing complexities of clinical trials. Digital platforms such as Interactive Response Technology (IRT), cloud-based inventory systems, and IoT-enabled tracking tools are becoming essential in enhancing supply chain responsiveness and transparency. These platforms provide real-time insights into drug availability, temperature control, and shipment progress, enabling supply managers to proactively address issues such as stockouts, wastage, and delays.
Real-time monitoring tools ensure compliance with stringent regulatory requirements by capturing data on temperature excursions, delivery confirmations, and chain-of-custody records. This is especially important for sensitive investigational products like biologics and personalized therapies. Predictive analytics integrated with these digital systems can forecast demand fluctuations and help optimize resupply strategies, improving trial continuity. Sponsors gain greater control, reducing risks and enhancing the patient experience by ensuring timely and reliable delivery of trial materials.
In this report, the Global Clinical Trial Supplies 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 Global Clinical Trial Supplies Market.
Global Clinical Trial Supplies 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: