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市场调查报告书
商品编码
1754272
2025 年至 2033 年生物製程验证市场规模、份额、趋势及预测(按测试类型、製程组件、最终用户和地区)Bioprocess Validation Market Size, Share, Trends and Forecast by Test Type, Process Component, End User, and Region, 2025-2033 |
2024年,全球生物製程验证市场规模为3.9183亿美元。展望未来, IMARC Group估计,到2033年,该市场规模将达到7.6167亿美元,2025年至2033年期间的复合年增长率为7.28%。北美目前占据市场主导地位,2024年的市占率将超过38.9%。生物製药产量的不断增长、严格监管要求的实施、技术的快速进步以及合约製造组织(CMO)的显着增长,都是支撑生物製程验证市场份额的一些因素。
全球生物製程验证市场需求正在显着成长,这主要得益于生物製药产量的不断增长。 2023年,欧洲药品管理局 (EMA) 批准了77种人用药物,其中39种含有新型活性物质,反映出生物製药开发管道的强劲成长。预计这一上升趋势将持续到2024年和2025年,届时将有大量生物製剂和生物相似药获得批准。生物製药生产的扩张进一步扩大了对严格生物製程验证的需求,以确保这些疗法的品质、安全性和有效性。製程验证、分析方法验证和清洁验证正成为合规框架的重要组成部分,尤其是在製造流程因采用连续生物製程、一次性技术和自动化而变得更加复杂的情况下。
美国生物製程验证市占率在各方面均呈现显着成长,目前已占据88.90%的市场。尤其值得一提的是,美国食品药物管理局(FDA)对所有生物製药生产都颁布了严格的法规,要求进行广泛的验证以确保产品的安全性、有效性和市场准入。随后,FDA于2025年1月发布了更新指南,其中将生物标记的生物分析方法验证确认为药物故障排除和开发过程中的一项严格要求,并製定了相应的验证方案。此外,FDA生物统计办公室在生物製药上市前审查中发挥重要作用,负责制定分析方法以评估所有药物的安全性和有效性,同时鼓励对已进行的验证进行全面、可靠的证据验证。监管方面的这些进步,加上生物製药产品日益复杂,将增加美国对先进生物製程验证服务的需求。
严格的监管要求
近年来,监管机构加强了对製程验证的重视,以确保生物製药的安全性和有效性。 2025年1月,美国食品药物管理局 (FDA) 发布了《生物标记生物分析方法验证》指南,为验证药物开发中使用的生物分析方法提供了详细建议。同样,欧洲药品管理局 (EMA) 在其指南中也强调了工艺验证的重要性,并强调了在监管提交中提供全面验证资料的必要性。这些严格的监管要求迫使生物製药公司在验证流程上投入大量资金,推动了全球生物製程验证市场的成长。
技术进步
2024年和2025年,技术进步显着推动了全球生物製程验证市场的发展。世界各国政府已发布多项指南,强调生物製程领域对先进验证技术的需求。此外,国际协调会(ICH)推出了关于生物分析方法验证的M10指南,该指南已被欧洲药品管理局(EMA)等监管机构采纳。该指南为验证生物分析检测提供了一个框架,促进了创新技术在生物製程验证中的应用。此外,美国食品药物管理局(FDA)于2024年3月采纳了第一版ISO 17665标准,该标准制定了医疗器械灭菌工艺的开发、验证和控制指南,彰显了其致力于加强生物工艺灭菌验证技术的决心。这些监管发展凸显了人们日益依赖尖端技术来确保生物製药产品的有效性和安全性。
合约製造组织(CMO)的成长
合约开发与生产组织 (CDMO) 的扩张显着影响全球生物製程验证市场。过去十年,CDMO 在生物製药领域发挥着举足轻重的作用,为 80% 以上经 FDA 和 EMA 批准的新分子实体 (NME) 的开发做出了贡献。自 2017 年以来,CDMO 已生产了超过 55% 的 NME,其中包括关键疫苗和治疗药物。目前,西方市场分销的所有药物、疫苗和非处方药中约有 40% 由 CDMO 生产。这种大规模的参与凸显了 CDMO 在高效合规的生物工艺方面日益增长的依赖,从而推动了对全面验证服务的需求,以确保产品品质和法规合规性。
The global bioprocess validation market size was valued at USD 391.83 Million in 2024. Looking forward, IMARC Group estimates the market to reach USD 761.67 Million by 2033, exhibiting a CAGR of 7.28% from 2025-2033. North America currently dominates the market, holding a market share of over 38.9% in 2024. The growing production of biopharmaceuticals, implementation of strict regulatory requirements, rapid technological advancements, and significant growth in contract manufacturing organizations (CMOs), are some of the factors bolstering the bioprocess validation market share.
The global bioprocess validation market demand is experiencing significant growth, primarily driven by the increasing production of biopharmaceuticals. In 2023, the European Medicines Agency (EMA) approved 77 medicines for human use, with 39 containing a novel active substance, reflecting a strong biopharmaceutical development pipeline. This upward trend is expected to continue into 2024 and 2025, with numerous biologics and biosimilars anticipated to receive approval. The expansion of biopharmaceutical production further amplifies the demand for rigorous bioprocess validation, which ensures the quality, safety, and efficacy of these therapeutics. Process validation, analytical method validation, and cleaning validation are becoming essential components of compliance frameworks, particularly as manufacturing processes grow more sophisticated with the adoption of continuous bioprocessing, single-use technologies, and automation.
The bioprocess validation market share in the United States is recording clear growth from various aspects, holding 88.90% market share. In particular, the US FDA has issued stringent regulations for any manufacture of biopharmaceuticals, which demand for extensive validation to ascertain product safety, efficacy, and approval in the market. Later on, in January 2025, an updated guidance by the FDA was released, in which bioanalytical method validation for biomarkers has been recognized as a stringent need with established protocols during troubleshooting and development of drugs. Also, yet the FDA's Office of Biostatistics plays to the great role of developing an analysis to consider the safety and efficacy of any medications in biopharmaceutical pre-market reviews, ever the whole of verifying sound evidence of the validations undertaken extensively is encouraged. Such regulatory strides, combined with the growing complexity of the biopharmaceutical products, will increase the demand for advanced bioprocess validation services in the United States.
Stringent Regulatory Requirements
In recent years, regulatory agencies have intensified their focus on process validation to ensure the safety and efficacy of biopharmaceuticals. In January 2025, the U.S. Food and Drug Administration (FDA) released the "Bioanalytical Method Validation for Biomarkers" guidance, providing detailed recommendations for validating bioanalytical methods used in drug development. Similarly, the European Medicines Agency (EMA) has emphasized process validation in its guidelines, underscoring the necessity for comprehensive validation data in regulatory submissions. These stringent regulatory requirements compel biopharmaceutical companies to invest significantly in validation processes, thereby driving the global bioprocess validation market growth.
Technological Advancements
In 2024 and 2025, technological advancements have significantly bolstered the global bioprocess validation market. Governments worldwide have released several guidelines, which underscores the need for advanced validation techniques in bioprocessing. Additionally, the International Council for Harmonisation (ICH) introduced the M10 guideline on bioanalytical method validation, which has been adopted by regulatory bodies like the European Medicines Agency (EMA). This guideline provides a framework for validating bioanalytical assays, promoting the adoption of innovative technologies in bioprocess validation. Additionally, the FDA's adoption of the first edition of ISO 17665 in March 2024, which establishes guidelines for developing, validating, and controlling medical device sterilization processes, underscores its dedication to enhancing sterilization validation techniques in bioprocessing. These regulatory developments highlight the increasing reliance on cutting-edge technologies to ensure the efficacy and safety of biopharmaceutical products.
Growth in Contract Manufacturing Organizations (CMOs)
The expansion of Contract Development and Manufacturing Organizations (CDMOs) significantly influences the global bioprocess validation market. Over the past decade, CDMOs have been pivotal in the biopharmaceutical sector, contributing to the development of over 80% of New Molecular Entities (NMEs) approved by the FDA and EMA. Since 2017, they have produced more than 55% of NMEs, including critical vaccines and treatments. Currently, CDMOs manufacture approximately 40% of all drug doses, vaccines, and over-the-counter products distributed in Western markets. This substantial involvement underscores the growing reliance on CDMOs for efficient and compliant bioprocesses, thereby driving the demand for comprehensive validation services to ensure product quality and regulatory adherence.
Based on the recent bioprocess validation market forecast, extractables testing services have the lion's share of the market, accounting for the cause of heightened veterinary scrutiny towards ensuring that a product is proven safe and efficacious for bioprocess validation. Regulatory bodies recommend comprehensive extractables and leachables examinations to identify contaminants in manufacturing subcomponents, such as filters and tubing, which directly affect the purity of drugs. These intricate procedures ensure compliance with GMPs and lower the risk of possible side effects for patients. Thanks to the ever-complicated nature of biopharmaceuticals and the burgeoning popularity of single-use systems in manufacturing, demand for extractables testing services is on the rise, and this has consequently solidified their position at the forefront of the market.
Filter elements are critical elements in bioprocess validation, with high significance in assuring product purity, sterility, and compliance with guideline standards. Filtration is widely used in biopharmaceutical manufacturing for the removal of particulates, microbial contaminants, and endotoxins in the production of raw materials, intermediates, and final drug formulations. With the increasing production of biologics, vaccines, and gene therapies, there came a lot of demand for better filtration systems. Membrane filters, depth filters, and sterile filters are among the most commonly used filter elements in bioprocessing. Any removed contending into cell culture media, buffer, or a final drug product can guarantee its integrity. The emergence of single-use filtration systems is also in demand owing to their economy on the material used, reduced risk of cross-contamination, and convenience of use under GMP conditions.
As per the latest bioprocess validation market outlook, pharmaceutical and biotechnology companies account for the largest share of the bioprocess validation market, due to rigid quality control measures, compliance with standards, and innovation. These companies devote large amounts of funding to research and development, with a view to bringing biologics, biosimilars, and gene therapies to market. Biologics and gene therapies require extensive validation to show that their use is safe and effective. Increased demand for mAbs, vaccines, cell and gene therapies, and recombinant proteins increases the demand for robust bioprocess validation services. Various regulatory agencies such as U.S. FDA, EMA, and ICH operate under very stringent regulations, requiring biopharmaceutical companies to validate processes-protocols-from upstream fermentation processes to downstream purification-in order to produce reliable products. Any change in the affiliated process parameters will affect the product's consistency, which in turn increases emphasis on validation during drug manufacturing. Advances in single-use bioprocessing systems, automation, and digital biomanufacturing are giving rise to the use of new analytical tools that enable process validation through real-time monitoring.
North America represented the largest share, with about 38.9% of the overall global bioprocess validation market. Factors leading to this region's dominance are majorly attributed to the leading biopharmaceutical companies, stringent regulatory framework, and major investments in R&D. Agencies such as the FDA and Health Canada enforce strict guidelines over the manufacturing of biologics that require some level of validation in order to ensure compliance with GMP. The demands of these agencies directly relay into a demand for validation services, particularly in process development, quality assurance, and risk mitigation. Other factors benefiting North America include an established biopharmaceutical industry, where several big players are investing in new biologics, biosimilars, and gene therapies. The rising adoption of advanced bioprocessing technologies-such as single-use systems, automation, and AI-driven analytics-is giving the necessary boost to this market. Growth of CDMOs in North America has also led to a demand for third-party validation services in compliance with regulatory standards for services confirming operational excellence.
United States Bioprocess Validation Market Analysis
The U.S. bioprocess validation market is expanding due to the strict regulatory requirements by the U.S. Food and Drug Administration (FDA) for biopharmaceutical production. The comprehensive validation studies required in the Biologics License Application (BLA) process have propelled the demand for validation services. The existing robust biopharmaceutical industry, where a large portion of the companies are heavily investing in optimizing their production processes, is driving adoption. The biopharmaceutical industry in the U.S. is a major contributor to the economy, accounting for around 1.6% of the nation's GDP, as per reports. Furthermore, scaling up production around monoclonal antibodies (mAb) and cell and gene therapies will call for the implementation of advanced methodologies for bioprocess validation to guarantee product quality and efficacy. Besides that, investments in research and development (R&D), the provision of government funds, and public-private partnerships bolster innovations in bioprocess validation technologies. Furthermore, the trend towards single-use bioprocessing will offer any rigorous validation required to overcome these sources of contamination and ensure reproducibility an encouraging outlook. Moreover, as biomanufacturing becomes more complex, furthered by the introduction of continuous processes and increased automation, a larger obligation arises for extensive validation protocols. In addition, the validation has to cover all aspects from sourcing raw materials to licensing/batch release of the finished product for automated systems and continuous processes to work reliably. Key players in the country are striving to extend their service offerings to cater to the rising demand from the industry, thereby augmenting market growth.
Europe Bioprocess Validation Market Analysis
A very strong regulatory environment led by the European Medicines Agency (EMA) and the European Directorate for the Quality of Medicines & HealthCare (EDQM) creates a highly developed continuum of validation requirements for biologics and biosimilars. The long-established biopharmaceutical sector in the region, especially Germany, the UK, and France, fuels demand for process validation solutions. The growing demand for personalized medicine, cell and gene therapies, and next-generation biologics is leading to the establishment of stringent validation strategies for compliance. The gene therapy market in Europe is projected to grow at 12.8% CAGR during the forecast period of 2024-2032, according to the IMARC Group. Emerging investments and developments in biomanufacturing are pushing the expansion of the validation market. Quality-by-design (QbD) principles and real-time process monitoring initiatives in the European Union further drive trust in robust validation tools. Besides this, with the rising sustainability concerns globally, new validation innovations are founded on minimizing environmental impact, specifically in single-use technologies. Besides this, a supportive network of CDMOs and biopharma clusters in the region complements the validation market. CDMO is a third-party firm that offers specialized services in biomanufacturing like process development, scale-up, and production. As these organizations turn to advanced technologies, they seek to ensure consistency and quality in their processes by implementing robust validation protocols.
Asia Pacific Bioprocess Validation Market Analysis
The Asia Pacific bioprocess validation market is witnessing strong growth on account of the rapid expansion of biopharmaceutical manufacturing in countries like China, India, South Korea, and Japan. In addition, governing agencies in the region are promoting domestic biologics production through financial incentives and favorable regulations, increasing demand for validation services. Besides this, rising healthcare expenditure and a growing patient base drive the need for cost-effective biosimilars, leading manufacturers to focus on robust validation processes to meet international regulatory standards. As per the India Brand Equity Foundation (IBEF), India's public healthcare expenditure reached 1.9% of GDP in the financial year 2024. Moreover, the region's lower operational costs attract global biopharma companies, creating a surge in contract development and manufacturing organization (CDMO) activities, which require stringent process validation. Apart from this, the increasing adoption of single-use bioprocessing systems necessitates validation studies to ensure process reliability. Expansion of research institutes and academic collaborations with industry players further strengthens the market. These partnerships facilitate the exchange of knowledge, bringing cutting-edge scientific discoveries and technological innovations into the biomanufacturing sector. By combining academic expertise with industry experience, these collaborations help develop more efficient, reliable, and cost-effective validation methods. Furthermore, evolving regulatory frameworks, particularly in China and India, are aligning with global standards, reinforcing the necessity of extensive bioprocess validation protocols.
Latin America Bioprocess Validation Market Analysis
The Latin American bioprocess validation market is growing due to increasing biopharmaceutical production in countries like Brazil, Mexico, and Argentina. Government initiatives supporting local biologics manufacturing and biosimilar development drive validation requirements. In line with this, rising investments in biotech startups and CDMOs is contributing to the market expansion. Reports indicate a substantial rise in venture capital investments in biotech across Brazil and Latin America, with Brazil accounting for over 60% of the region's share in 2023. Furthermore, the region is aligning its regulatory frameworks with international standards, prompting manufacturers to enhance validation procedures. Growing demand for vaccines and monoclonal antibodies is boosting process validation needs. Additionally, the rising adoption of single-use bioprocessing systems is increasing the need for validation services to ensure sterility and efficiency.
Middle East and Africa Bioprocess Validation Market Analysis
The growing pharmaceutical and biopharmaceutical manufacturing sectors in the UAE, Saudi Arabia, and South Africa are driving market expansion. In the Middle East and Africa's pharmaceutical industry, 16 M&A deals were announced in Q3 2024, totaling USD 1.8 billion, according to reports. In addition, government initiatives promoting local vaccine and biosimilar production are increasing validation requirements. The region's improving regulatory landscape, with agencies striving to meet global quality standards, is encouraging rigorous validation processes. Furthermore, growing investments in biotechnology research and partnerships with global biopharma companies further support the market growth. Apart from this, the rise in chronic diseases and demand for biologics is pushing manufacturers to adopt validated bioprocessing solutions for quality assurance.
Key players in the bioprocess validation market are adopting strategic initiatives to reinforce their market presence and address the evolving needs of the biopharmaceutical sector. They are investing in advanced technologies to optimize validation processes while maintaining compliance with strict regulatory requirements. Collaborations and partnerships are being formed to expand service offerings and global reach. Additionally, companies are focusing on integrating digital solutions and automation to improve efficiency and data accuracy in validation procedures. These initiatives indicate a commitment to innovation, quality assurance, and the expansion of capabilities to support the growing complexity of biopharmaceutical products.