市场调查报告书
商品编码
1524275
活性药物成分 CDMO 市场 - 按产品、适应症、药物、工作流程、应用、最终用途 - 全球预测Active Pharmaceutical Ingredient CDMO Market - By Product, Indication, Drug, Workflow, Application, End-use - Global Forecast |
由于仿製药需求不断增加,RampD 计画激增,预计 2024 年至 2032 年全球活性药物成分 CDMO 市场规模将创下 6.6% 的复合年增长率。这些组织正在创新活性药物成分 API 合成和製程优化,以提高药物疗效和生产效率。
对仿製药的需求不断增长也推动 CDMO 扩大其能力和能力,以满足全球药品需求。不断努力开发具有成本效益的高品质 API,以利用连续製造和绿色化学等先进技术,将推动产业成长。例如,2022年3月,住友化学宣布兴建新的原料药生产工厂,计画于2024年9月投产,以增强其为小分子药物提供高品质原料药和中间体的能力。
活性药物成分 CDMO 市场分为产品、适应症、药物、工作流程、应用、最终用途和区域。
从产品来看,由于对生物药物的需求不断增长,生物 API 领域预计从 2024 年到 2032 年将大幅成长。 CDMO 正在利用先进的生物技术製程来製造复杂的生物分子,例如单株抗体和重组蛋白。生物加工技术也进行了创新,以提高生物 API 的产量、纯度和可扩展性。
由于迫切需要满足对有效动物保健产品日益增长的需求,预计兽医应用领域的活性药物成分 CDMO 产业将在 2024 年至 2032 年期间扩大。这导致了专门用于兽药(包括抗生素、抗寄生虫药和疫苗)的 API 的更高开发和生产。 API CDMO 也利用先进技术来提高兽药的功效和安全性。
从地区来看,在药品供应链全球化和严格的监管合规要求的推动下,欧洲活性药物成分 CDMO 产业规模预计将在 2024 年至 2032 年间强劲成长。该地区的 CDMO 正在改进其製造工艺,以确保 API 无缝整合到全球供应链中,以满足多样化的国际标准。大量采用先进技术和实践来维持高品质的生产标准将推动欧洲市场的成长。
Global Active Pharmaceutical Ingredient CDMO Market size is predicted to record 6.6% CAGR from 2024 to 2032, due to the surging R&D initiatives amidst the increasing demand for generic drugs. These organizations are innovating active pharmaceutical ingredient API synthesis and process optimization to enhance drug efficacy and production efficiency.
The rising demand for generic drugs is also driving CDMOs to expand their capabilities and capacities to meet the global pharmaceutical needs. Growing efforts on developing cost-effective and high-quality APIs for leveraging advanced technologies like continuous manufacturing and green chemistry will drive the industry growth. For instance, in March 2022, Sumitomo Chemical Co., Ltd. announced the construction of a new manufacturing plant for APIs, scheduled to come on stream in September 2024, to enhance its capacity to supply high-quality APIs and intermediates for small molecule drugs.
The active pharmaceutical ingredient CDMO market is segregated into product, indication, drug, workflow, application, end-use, and region.
By product, the biological APIs segment is estimated to rise at a significant rate from 2024 to 2032, due to the growing demand for biologic drugs. CDMO's are leveraging advanced biotechnological processes to manufacture complex biological molecules, such as monoclonal antibodies and recombinant proteins. There have also been innovations in bio-processing techniques to improve yields, purity, and scalability of biological APIs.
Active pharmaceutical ingredient CDMO industry from the veterinary application segment is expected to expand from 2024 to 2032 owing to the strong need for addressing the increasing need for effective animal health products. This has led to the higher development and manufacturing of APIs specifically for veterinary medicines including antibiotics, anti-parasitic, and vaccines. API CDMOs also leverage advanced technologies to improve the efficacy and safety of veterinary drugs.
Regionally, the Europe active pharmaceutical ingredient CDMO industry size is projected to witness robust growth between 2024 and 2032, propelled by the globalization of pharmaceutical supply chains and stringent regulatory compliance requirements. CDMO's in the region are enhancing their manufacturing processes to ensure the seamless integration of APIs into global supply chains for meeting the diverse international standards. Surging adoption of advanced technologies and practices to maintain high-quality production standards will drive the market growth in Europe.