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市场调查报告书
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1662632
2030 年生物製药自动化市场预测:按组件、自动化模式、技术、应用、最终用户和地区进行的全球分析Automation in Biopharma Market Forecasts to 2030 - Global Analysis By Component, Mode of Automation, Technology, Application, End User and By Geography |
根据 Stratistics MRC 的数据,预测期内全球生物製药自动化市场复合年增长率为 8.4%。
生物製药自动化是指利用先进的技术和系统来简化和优化生物製药生产中的各个流程。这包括自动化细胞培养、蛋白质生产、品管、资料分析和包装等任务。透过整合机器人、人工智慧和机器学习,自动化可以提高效率、减少人为错误、提高一致性并缩短新药的上市时间。自动化在确保生物製药行业的法规遵循和成本效益製造方面发挥关键作用。
个人化医疗需求日益增长
个人化医疗的需求不断增长,推动市场需求。个人化治疗,例如基因疗法和客製化生技药品,需要高度专业化和可扩展的製造流程,以满足个别患者的需求。自动化有助于精确控制这些复杂过程,确保一致性和效率。透过提高生产能力并减少人为错误,自动化可以帮助生物製药公司满足日益增长的个人化治疗需求,同时确保高品质标准。
资料安全和隐私问题
生物製药自动化中的资料安全和隐私问题可能导致重大风险,包括未授权存取敏感病患资讯、智慧财产权窃盗和不遵守法规。违规行为可能导致声誉受损、高额罚款以及失去相关人员的信任。资料保护不力也会阻碍创新和协作,因为公司可能不愿意共用关键讯息,最终减缓药物开发并影响市场竞争。
提高资料品质和一致性
提高市场资料的品质和一致性可以改善决策、法规遵循和业务效率。透过整合人工智慧和机器学习等先进技术,企业可以最大限度地减少人为错误,简化资料收集,并确保即时资料的准确性。这将带来更可靠的流程、更快的药物开发和优化的製造——最终缩短上市时间并降低成本,同时保持高品质和安全性。
初期投资成本高
市场上高昂的初始投资成本可能是中小企业面临的一大障碍。先进技术、设备和基础设施的高昂前期成本可能会减缓或阻碍其采用。这可能导致创新放缓、竞争减少和财务压力增加。小型企业可能难以获得融资,从而阻碍其扩大规模、提高效率和跟上行业巨头的能力。
COVID-19 疫情加速了市场发展,并凸显了对更快、更有效率的药物开发和製造流程的需求。自动化有助于简化疫苗製造、临床测试和供应链管理。然而,疫情扰乱了全球供应链,也导致新技术的采用出现延迟和挑战。儘管存在这些障碍,但这场危机凸显了自动化在增强生物製药业务的弹性和可扩展性方面的作用。
预计预测期内自动化软体部分将实现最大幅度成长。
预计预测期内自动化软体部分将占据最大的市场占有率。整合人工智慧、机器学习和资料分析等技术,以提高效率、减少错误并确保法规符合。透过自动执行重复任务,这些软体解决方案可以提高资料收集的准确性、加快生产进度并支援即时监控。这最终意味着生物製药产业成本降低、产品上市缩短时间、产品品质提升。
预计预测期内製药公司部门将以最高的复合年增长率成长。
预计製药公司部门在预测期内将呈现最高的成长率。整合机器人、人工智慧和机器学习等自动化工具可以提高准确性、减少人为错误并加快生产流程。这些公司专注于优化供应链、临床测试和品管。自动化不仅降低了营运成本,还加速了创新并缩短了关键治疗方法和疗法的上市时间。
由于技术进步以及对更高效的药物生产和开发流程的需求,预计北美地区将在预测期内占据最大的市场占有率。对人工智慧、机器人和资料分析的大力投资正在帮助北美公司优化製造、加强品管并确保法规合规。该地区注重创新,加上强大的医疗保健基础设施,使其成为生物製药自动化领域的全球领导者。
预计预测期内亚太地区将呈现最高的复合年增长率。对生技药品、生物相似药和先进疗法的需求不断增长,推动生物製药公司采用自动化技术来简化生产流程、提高一致性和规模化生产。此外,先进技术的发展增强了自动化系统,使其更易于生物製药行业使用和适应。
According to Stratistics MRC, the Global Automation in Biopharma Market is growing at a CAGR of 8.4% during the forecast period. Automation in biopharma is the use of advanced technologies and systems to streamline and optimize various processes in the production of biopharmaceuticals. This includes automating tasks such as cell culture, protein production, quality control, data analysis, and packaging. By integrating robotics, artificial intelligence, and machine learning, automation enhances efficiency, reduces human error, improves consistency, and accelerates time-to-market for new drugs. It plays a crucial role in ensuring regulatory compliance and cost-effective manufacturing in the biopharmaceutical industry.
Growing demand for personalized medicine
The growing demand for personalized medicine is driving the need for market. Personalized treatments require highly specific and scalable manufacturing processes to cater to individual patient needs, such as gene therapies and customized biologics. Automation facilitates the precise control of these complex processes, ensuring consistency, and efficiency. By enhancing production capabilities and reducing human error, automation enables biopharma companies to meet the increasing demand for tailored therapies, while ensuring high-quality standards.
Data security and privacy concerns
Data security and privacy concerns in biopharma automation can lead to significant risks, including unauthorized access to sensitive patient information, intellectual property theft, and regulatory violations. Breaches may result in reputational damage, costly fines, and loss of trust from stakeholders. Inadequate data protection can also hinder innovation and collaboration, as companies may be reluctant to share critical information, ultimately delaying drug development and affecting market competitiveness.
Improved data quality and consistency
Improved data quality and consistency in the market enhances decision-making, regulatory compliance, and operational efficiency. By integrating advanced technologies such as AI and machine learning, companies can minimize human errors, streamline data collection, and ensure real-time data accuracy. This leads to more reliable processes, faster drug development, and optimized manufacturing, ultimately accelerating time-to-market and reducing costs while maintaining high standards of quality and safety.
High initial investment costs
High initial investment costs in the market can be a significant barrier for smaller companies. The substantial upfront expenses for advanced technologies, equipment, and infrastructure may delay or prevent adoption. This can result in slower innovation, reduced competitiveness, and increased financial pressure. Smaller firms may struggle to secure funding, hindering their ability to scale operations, improve efficiency, and keep pace with larger industry players.
The COVID-19 pandemic accelerated the adoption of the market, highlighting the need for faster, more efficient drug development and manufacturing processes. Automation helped streamline vaccine production, clinical trials, and supply chain management. However, the pandemic also disrupted global supply chains, leading to delays and challenges in deploying new technologies. Despite these hurdles, the crisis underscored automation's role in enhancing resilience and scalability in biopharma operations.
The automation software segment is expected to be the largest during the forecast period
The automation software segment is expected to account for the largest market share during the forecast period. It integrates technologies like AI, machine learning, and data analytics to improve efficiency, reduce errors, and ensure regulatory compliance. By automating repetitive tasks, these software solutions enhance accuracy in data collection, speed up production timelines, and support real-time monitoring. This ultimately leads to lower costs, faster time-to-market, and higher product quality in the biopharma industry.
The pharmaceutical companies segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the pharmaceutical companies segment is predicted to witness the highest growth rate. By integrating automation tools like robotics, AI, and machine learning, they improve accuracy, reduce human error, and speed up production processes. These companies focus on optimizing supply chains, clinical trials, and quality control. Automation not only lowers operational costs but also accelerates innovation, ensuring faster time-to-market for critical therapies and treatments.
During the forecast period, the North America region is expected to hold the largest market share driven by technological advancements and the need for more efficient drug production and development processes. With strong investments in AI, robotics, and data analytics, North American companies are optimizing manufacturing, enhancing quality control, and ensuring regulatory compliance. The region's focus on innovation, coupled with a robust healthcare infrastructure, positions it as a global leader in biopharma automation.
Over the forecast period, the Asia Pacific region is anticipated to exhibit the highest CAGR. The growing demand for biologics, biosimilars, and advanced therapies is pushing biopharmaceutical companies to adopt automation technologies to streamline production processes, improve consistency, and meet high production volumes. Additionally, the development of advanced technologies has enhanced automation systems, making them more accessible and adaptable to the biopharmaceutical industry.
Key players in the market
Some of the key players in Automation in Biopharma market include Thermo Fisher Scientific Inc., Siemens Healthineers AG, Danaher Corporation, GE HealthCare Technologies Inc., PerkinElmer, Inc., Tecan Group Ltd., Sartorius AG, Agilent Technologies, Inc., Hamilton Company, Bio-Rad Laboratories, Inc., Eppendorf AG, Bruker Corporation, Honeywell International Inc., Parker Hannifin Corporation, Rockwell Automation, Inc., Waters Corporation and Yokogawa Electric Corporation.
In December 2024, Siemens Healthineers has concluded the acquisition from Novartis of Advanced Accelerator Applications Molecular Imaging, a European manufacturing and distribution network of diagnostic radiopharmaceuticals for positron emission tomography (PET) scans. The acquired company will be known as Advanced Accelerator Applications, a Siemens Healthineers company.
In June 2024, Thermo Fisher Scientific Inc., the world leader in serving science, today introduced the Thermo Scientific(TM) KingFisher(TM) PlasmidPro Maxi Processor* (PlasmidPro), the only fully automated maxi-scale plasmid DNA (pDNA) purification system. PlasmidPro enables innovation at scale, providing complete automation across mini and maxi scale purification and delivering high-purity plasmid without manual column preparation and intervention.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.