市场调查报告书
商品编码
1623742
临床试验材料和耗材市场规模、份额、成长分析,按服务、按阶段、按类型、按治疗领域、按地区 - 行业预测,2025-2032Clinical Trial Materials And Supplies Market Size, Share, Growth Analysis, By Service (Logistics & Distribution, Storage & Retention), By Phase (Phase I, Phase II), By Type, By Therapeutic Area, By Region - Industry Forecast 2025-2032 |
2023年临床试验材料和耗材的全球市场规模预计为35亿美元,从2024年的38.4亿美元增长到2032年的81.2亿美元,在预测期内(2025-2032年)预计将以2018 年复合年成长率为9.8%)。
管理临床试验用品对于避免缺货和生产过剩等问题至关重要,尤其是在药物检测成本增加的情况下。有效的供应链管理对于临床研究至关重要,并且必须解决基础设施限制和严格的法规。主要市场驱动因素包括临床试验的扩展和复杂性。临床试验用品包括输液帮浦、雾化器、针头等多种设备,对于心血管、神经、肿瘤、肺部领域疾病的评估和治疗至关重要。药物开发商和製造商越来越多地外包耗材,以确保及时交付到临床实验试验场所。此外,技术进步、解决方案提供者的策略性成长以及专利到期日的增加都刺激了对临床试验材料的需求,并促进了市场的强劲成长。
Global Clinical Trial Materials And Supplies Market size was valued at USD 3.5 billion in 2023 and is poised to grow from USD 3.84 billion in 2024 to USD 8.12 billion by 2032, growing at a CAGR of 9.8% during the forecast period (2025-2032).
The management of clinical trial supplies is critical to avert issues such as inventory expiration and overproduction, especially as drug detection costs rise. Effective supply chain management is essential in clinical research, addressing infrastructure limitations and stringent regulations. Key market drivers include the expansion and growing complexity of clinical trials. Clinical trial supplies encompass various instruments like infusion pumps, nebulizers, and syringe needles, pivotal for evaluating and treating diseases across cardiovascular, neurological, oncological, and pulmonary fields. Outsourcing of supplies by drug developers and manufacturers is increasing, ensuring timely delivery to investigator sites. Additionally, technological advancements, strategic growth among solution providers, and a rise in patent expirations have fueled demand for clinical trial materials, contributing to robust market growth.
Top-down and bottom-up approaches were used to estimate and validate the size of the Global Clinical Trial Materials And Supplies market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Clinical Trial Materials And Supplies Market Segmental Analysis
Global Clinical Trial Materials And Supplies Market is segmented by service, phase, type, therapeutic area, end user and region. Based on service, the market is segmented into logistics & distribution, storage & retention, packaging, labelling & blinding, manufacturing, comparator sourcing and other services. Based on phase, the market is segmented into Phase I, Phase II, Phase III, Phase IV, BA/BE Studies. Based on type, the market is segmented into small-molecules, biologic drugs and medical devices. Based on therapeutic area, the market is segmented into oncology, infectious diseases, neurology, metabolic disorders, immunology, cardiology, genetic diseases and other therapeutic areas. Based on end user, the market is segmented into pharmaceutical and biotechnology companies, contract research organisations (CRO's) and medical device companies. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Global Clinical Trial Materials And Supplies Market
The Global Clinical Trial Materials and Supplies market is significantly driven by the increasing participation of patients in clinical trials within emerging economies such as China, India, and South Korea. The lower costs associated with conducting clinical trials in these nations-28% cheaper before tax incentives and a remarkable 60% less expensive after tax incentives compared to the United States-have attracted pharmaceutical companies seeking to optimize their research expenditures. This trend has also led to a shift in clinical trial locations, particularly for rare diseases. Furthermore, advancements in technology and data analytics contribute to improved decision-making in clinical trials, prompting the pharma and biotech sectors to invest in outsourcing innovative solutions that enhance trial processes and supply chains in these developing markets.
Restraints in the Global Clinical Trial Materials And Supplies Market
The Global Clinical Trial Materials and Supplies market faces considerable restraints primarily due to the high attrition rates of drug candidates during development, which lead to immense research and development costs. The complexities associated with R&D for rare diseases often require specialized personnel to conduct clinical trials, further complicating the process. For instance, only 7 out of 100 cancer drugs that reach clinical trials ultimately gain regulatory approval, with most drug candidates failing before this stage. Additionally, the entire journey from drug discovery to FDA approval can span 10-15 years and incur costs around USD 2.6 billion, with less than 12% of candidates reaching Phase clinical trials successfully, posing significant challenges to market expansion.
Market Trends of the Global Clinical Trial Materials And Supplies Market
The Global Clinical Trial Materials and Supplies market is witnessing a notable trend towards the increased utilization of biologics and temperature-sensitive medications, with approximately 35% of late-phase pharmaceutical drugs classified as biologics, alongside 38% being temperature-sensitive. This shift is largely attributed to the advantages biologics offer, including fewer side effects compared to traditional pharmaceuticals. With the expectation that the prevalence of biologics will continue to rise, there is a corresponding surge in demand for advanced cold chain logistics and storage solutions to ensure the efficacy and safety of these sensitive materials during clinical trials, thereby shaping the future landscape of the market.