![]() |
市场调查报告书
商品编码
1769601
医药品中间体CDMO的全球市场:各用途,中间体类别,医药品类别,各地区 - 2035年前的预测分析Global Pharmaceutical Intermediate CDMO Market Research Report by Application, by Type of Intermediate, by Drug Type, and by Region Forecast Analysis till 2035 |
2024年,全球医药中间体CDMO市场规模为1,617.989亿美元。预计2024年至2035年,该市场规模将达3,467.443亿美元,复合年增长率为7.4%。
受多种因素影响,全球医药中间体CDMO市场正快速扩张。製药公司为提高效率和减轻营运负担,越来越多地采用外包模式。对仿製药和生物相似药的需求日益增长,尤其是在中低收入国家,是主要的成长因素。此外,中间体合成技术的进步和新药製剂的复杂性,促使企业寻求专业的CDMO支援。新兴国家医疗基础设施的建设也促进了市场的发展。
另一方面,严格的监管合规要求和漫长的审批週期往往会阻碍进展。高昂的资本和营运成本、智慧财产权相关风险以及持续的供应链中断都是显着的障碍。缺乏先进的化学专业知识也是一个课题。儘管存在这些问题,但透过与生物技术公司建立策略合作伙伴关係,以及对客製化、患者专用药物解决方案日益增长的需求,该市场仍然存在着广阔的机会。
产业区隔
按应用领域,全球市场细分为肿瘤学、心血管疾病、中枢神经系统和神经系统疾病以及传染病。
依药物类型,全球医药中间体 CDMO 市场包括仿製药和品牌药。
全球医药中间体 CDMO 市场按中间体类型细分,包括活性药物成分 (API)、生物中间体、辅料和添加剂以及核苷酸中间体。
依地区划分,全球医药中间体CDMO市场分为北美、欧洲、南美、中东和非洲、亚太地区。
北美医药中间体CDMO市场规模最大、发展最成熟,其中美国凭藉其高科技基础设施、巨额研发投入以及FDA严格的品质监管而处于领先地位。加拿大生物製药产业的成长进一步增强了该地区的实力。
欧洲既迎合国内巨头,也迎合全球企业,注重法规合规性、复杂合成的创新以及符合循环经济原则的可持续生产方法。
以中国和印度为首的亚太地区是成长最快的地区。经济高效的製造、大规模的设施和一体化的供应链使具有竞争力的中间体生产成为可能。
拉丁美洲各国面临不同的监管框架,但正在透过区域合作努力实现统一的标准。具有竞争力的劳动力成本和靠近美国的地理位置是其优势,但基础设施的限制在一定程度上阻碍了其成长。
在中东和非洲,CDMO主要透过生产仿製药和基本药物的中间体来服务当地和邻近市场。该地区位于亚洲和欧洲之间,预计将成为医药物流和中间体供应的潜在枢纽。随着全球供应链的发展,中东和非洲地区作为跨洲製造桥樑的角色可能会更加突出。
赛默飞世尔科技、Raghava Life Sciences Pvt LTD.、Cambrex Corporation、Actylis、Chiracon GmbH、Codexis, Inc.、Arkema S.A.、龙沙集团、康泰伦特和浙江九洲药业股份有限公司是全球医药中间体CDMOMO市场的主要竞争对手。
本报告调查了全球医药中间体CDMO市场,并提供了市场概况、按应用、中间体类型、药品类型和地区划分的趋势以及参与市场的公司概况。
Global Pharmaceutical Intermediate CDMO Market Research Report by Application (Oncology, Cardiovascular Diseases, CNS & Neurological Disorders, Infectious Diseases), by Type of Intermediate [Active Pharmaceutical Ingredients (APIs), Excipients and Additives, Biologics Intermediates, Nucleotide Intermediates], by Drug Type (Generic Drugs, Branded Drugs), and by Region (North America, Europe, South America, Middle East and Africa, and Asia Pacific) Forecast Analysis till 2035
Industry Overview
In 2024, global pharmaceutical intermediate CDMO market was valued at USD 161,798.9 million. It is projected to increase at a compound annual growth rate (CAGR) of 7.4% from 2024 to 2035, reaching USD 346,744.3 million.
The global market for Pharmaceutical Intermediate CDMOs is expanding rapidly due to various contributing factors. Outsourcing by pharmaceutical firms is on the rise as they aim to enhance efficiency and reduce operational burdens. The increasing need for generic drugs and biosimilars, especially in low- and middle-income countries, is a major growth driver. Additionally, advancements in intermediate synthesis technologies and the complex nature of new drug formulations are pushing companies toward specialized CDMO support. The growth of healthcare infrastructure in emerging economies is also enhancing the market landscape.
On the flip side, stringent regulatory compliance requirements and lengthy approval timelines often hamper progress. High capital and operational expenses, intellectual property-related risks, and ongoing supply chain disruptions present notable barriers. A shortage of expertise in advanced chemistry remains another challenge. Despite these issues, the market holds promising opportunities through strategic alliances with biotechnology companies and the increasing demand for tailored, patient-specific medicine solutions.
Industry Segmentations
In terms of application types, the global market is divided into oncology, cardiovascular diseases, CNS and neurological disorders, and infectious disease.
Based on the drug type, global pharmaceutical intermediate CDMO market comprises generic drugs, branded drug.
Global Pharmaceutical intermediate CDMO market has been categorized by type of intermediate, includes active pharmaceutical ingredients (APIS), biologics intermediates, excipients and additives, nucleotide intermediates.
Regionally, global pharmaceutical intermediate CDMO market divided into North America, Europe, South America, Middle East and Africa, and Asia Pacific.
The North American market for pharmaceutical intermediate CDMOs is the largest and most sophisticated, with the U.S. leading due to high-tech infrastructure, heavy R&D investments, and FDA-enforced quality regulations. Canada's rising biopharmaceutical industry further supports regional strength.
Europe caters to both domestic powerhouses and global players, emphasizing regulatory compliance, innovation in complex syntheses, and sustainable production practices aligned with circular economy principles.
Asia Pacific, spearheaded by China and India, is witnessing the fastest growth. Cost-effective manufacturing, large-scale facilities, and integrated supply chains enable competitive production of intermediates.
Latin America, while facing diverse regulatory frameworks across countries, is working toward unified standards through regional cooperation. Competitive labor costs and proximity to the U.S. are advantageous, though growth is somewhat hindered by infrastructure constraints.
In the Middle East and Africa, CDMOs largely serve local and neighboring markets by producing intermediates for generic medicines and essential drugs. The region's favorable location between Asia and Europe positions it as a potential hub in pharmaceutical logistics and intermediate supply. As global supply chains evolve, MEA's role may become more pronounced in bridging manufacturing efforts across continents.
Thermo Fisher Scientific, Raghava Life Sciences Pvt LTD., Cambrex Corporation, Actylis, Chiracon GmbH, Codexis, Inc., Arkema S.A., Lonza Group AG, Catalent, Inc., Zhejiang Jiuzhou Pharmaceutical Co Ltd are the key competitors of the global pharmaceutical intermediate CDMO market.