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市場調查報告書
商品編碼
1769601
醫藥品中間體CDMO的全球市場:各用途,中間體類別,醫藥品類別,各地區 - 2035年前的預測分析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,全球醫藥中間體CDMO市場規模為1,617.989億美元。預計2024年至2035年,該市場規模將達3,467.443億美元,複合年增長率為7.4%。
受多種因素影響,全球醫藥中間體CDMO市場正快速擴張。製藥公司為提高效率和減輕營運負擔,越來越多地採用外包模式。對仿製藥和生物相似藥的需求日益增長,尤其是在中低收入國家,是主要的成長因素。此外,中間體合成技術的進步和新藥製劑的複雜性,促使企業尋求專業的CDMO支援。新興國家醫療基礎設施的建設也促進了市場的發展。
另一方面,嚴格的監管合規要求和漫長的審批週期往往會阻礙進展。高昂的資本和營運成本、智慧財產權相關風險以及持續的供應鏈中斷都是顯著的障礙。缺乏先進的化學專業知識也是一個課題。儘管存在這些問題,但透過與生物技術公司建立策略合作夥伴關係,以及對客製化、患者專用藥物解決方案日益增長的需求,該市場仍然存在著廣闊的機會。
產業區隔
按應用領域,全球市場細分為腫瘤學、心血管疾病、中樞神經系統和神經系統疾病以及傳染病。
依藥物類型,全球醫藥中間體 CDMO 市場包括仿製藥和品牌藥。
全球醫藥中間體 CDMO 市場按中間體類型細分,包括活性藥物成分 (API)、生物中間體、輔料和添加劑以及核苷酸中間體。
依地區劃分,全球醫藥中間體CDMO市場分為北美、歐洲、南美、中東和非洲、亞太地區。
北美醫藥中間體CDMO市場規模最大、發展最成熟,其中美國憑藉其高科技基礎設施、巨額研發投入以及FDA嚴格的品質監管而處於領先地位。加拿大生物製藥產業的成長進一步增強了該地區的實力。
歐洲既迎合國內巨頭,也迎合全球企業,注重法規合規性、複雜合成的創新以及符合循環經濟原則的可持續生產方法。
以中國和印度為首的亞太地區是成長最快的地區。經濟高效的製造、大規模的設施和一體化的供應鏈使具有競爭力的中間體生產成為可能。
拉丁美洲各國面臨不同的監管框架,但正在透過區域合作努力實現統一的標準。具有競爭力的勞動力成本和靠近美國的地理位置是其優勢,但基礎設施的限制在一定程度上阻礙了其成長。
在中東和非洲,CDMO主要透過生產仿製藥和基本藥物的中間體來服務當地和鄰近市場。該地區位於亞洲和歐洲之間,預計將成為醫藥物流和中間體供應的潛在樞紐。隨著全球供應鏈的發展,中東和非洲地區作為跨洲製造橋樑的角色可能會更加突出。
賽默飛世爾科技、Raghava Life Sciences Pvt LTD.、Cambrex Corporation、Actylis、Chiracon GmbH、Codexis, Inc.、Arkema S.A.、龍沙集團、康泰倫特和浙江九洲藥業股份有限公司是全球醫藥中間體CDMOMO市場的主要競爭對手。
本報告調查了全球醫藥中間體CDMO市場,並提供了市場概況、按應用、中間體類型、藥品類型和地區劃分的趨勢以及參與市場的公司概況。
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.