USD 5.3 billion
Report ID:
SQMIG35A3058 |
Region:
Global |
Published Date: July, 2025
Pages:
193
|Tables:
92
|Figures:
71
Global Virus Filtration Market size was valued at USD 5.3 billion in 2023 and is poised to grow from USD 5.85 billion in 2024 to USD 12.81 billion by 2032, growing at a CAGR of 10.3% during the forecast period (2025-2032).
The global virus filtration market is witnessing robust expansion, primarily driven by the escalating demand for biologics that necessitate stringent viral safety measures. As biopharmaceutical companies intensify efforts to develop advanced therapies, virus filtration has become indispensable to ensure the purity of products such as monoclonal antibodies and recombinant proteins. This growing emphasis on viral clearance is further supported by rising R&D expenditures and favourable government initiatives aimed at strengthening biomanufacturing capabilities.
One of the key trends driving the global virus filtration market is the emphasis on technological innovation. Key players are investing in next-generation membrane technologies such as nanofiber and single-use filter systems, that enhance throughput and reduce contamination risks. Concurrently, the market is diversifying beyond traditional biologics into applications within medical devices, water treatment, and air purification, broadening the scope of virus filtration solutions. In addition, automation of filtration workflows and integration with continuous bioprocessing platforms is accelerating adoption, as manufacturers seek to minimize manual interventions and contamination risks. Furthermore, strategic collaborations between filter manufacturers and bioprocessing firms are driving co-development of tailored solutions, enabling faster scale-up of novel biologics and fostering advancements in filter validation protocols to ensure robust viral clearance across diverse production scales.
How AI is Enhancing the Quality Control & Maintenance Standards in Global Market?
AI is changing virus filtration by providing real-time tracking and predictive maintenance for filtration operations. Leading manufacturers are developing operational AI-based sensors to use in filtration units, so that they can continuously measure membrane integrity and be made aware of possible viral breakthroughs in advance. Predicting breakthroughs will allow for improvements in filter or part replacement schedules and product recall reductions.
A recent development illustrating AI’s impact is the trend of models evolving recently to use machine-learning algorithms. That study filtration parameters to determine when a filter is nearing a time where its performance may degrade. A number of manufacturers are developing AI models to monitor multivariate data obtained (pressure flow and turbidity) to be interpreted with predictive models to calculate viral clearance performance. The early AI-based systems have been shown to allow users to have a 20% greater filter life, and a 15% reduction in unplanned downtimes.
There are many applications of AI for performance and efficiency, but AI is also being used for the development of new-quality membrane materials, developed from nanoscale patterning, computational models provide the best pure form that provides higher flow and viral retention. The tandem combination of AI and material science suggests that next-generation filters will be designed to handle greater material volume with no loss of safety.
Market snapshot - 2025-2032
Global Market Size
USD 5.3 billion
Largest Segment
Consumables
Fastest Growth
Services
Growth Rate
10.3% CAGR
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Global Virus Filtration Market is segmented by Product, Application, End User and region. Based on Product, the market is segmented into Kits and Reagents, Filtration Systems, Services and Other Products. Based on Application, the market is segmented into Biologicals, Medical Devices, Water Purification and Air Purification. Based on End User, the market is segmented into Pharmaceutical & Biotechnology Companies, Contract Research Organizations, Academic Research Institutes and Medical Device Companies. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Within the Product segment, consumables, comprising of kits, reagents, and membrane filters, hold the majority share in the global virus filtration market. Driven by its indispensable role in downstream viral clearance during biologics manufacturing. Consumables are single-use, reducing cross-contamination risk, and support high-throughput screening in R&D. Their recurring purchase model also bolsters vendor revenues, as biopharma firms continuously invest in novel therapies that require stringent viral safety measures.
According to our global virus filtration market analysis, services, which include validation studies, maintenance, and consulting, are expanding most rapidly within the product segment in the global virus filtration market. As manufacturers outsource complex viral clearance validation to specialized providers, demand for contract services spikes. This trend is propelled by increasingly stringent regulatory expectations for filter certification, prompting many organizations to rely on external expertise rather than build in-house capabilities.
The biologicals application, encompassing vaccines, monoclonal antibodies, gene therapy vectors, and cell therapy products, commands the largest share of applications segment of the global virus filtration market. Biologics require rigorous viral removal steps, making virus filtration essential during downstream purification. As major pipelines shift toward mRNA and recombinant proteins, consumption of virus-removal filters within biologicals production has surged. Moreover, heightened regulatory scrutiny around viral safety for injectable products has cemented Biologicals as the top application by far.
Medical Devices is the fastest growing application in the global virus filtration industry. Increased focus on sterilizing device components such as infusion filters and implantable catheters, has driven adoption of virus-grade membranes. Innovations in single-use filter cartridges tailored for device manufacturing are expanding rapidly, supported by rising infection-control standards in hospitals and outpatient centers. Consequently, this sub-segment is outpacing others due to evolving regulatory requirements and investment in point-of-care diagnostic tools.
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North America leads the global virus filtration market due to its advanced biopharmaceutical infrastructure, stringent regulatory environment, and high healthcare expenditure. The region benefits from well-established manufacturing hubs and early adoption of next-generation filtration technologies, such as single-use systems and nanofiber membranes, which streamline downstream purification workflows. Large-scale investment in R&D and robust collaboration between academic institutions and industry players further bolster market dominance. Additionally, favorable government policies and dedicated funding for biologics development ensure North America continues to set benchmarks for viral safety in biologics manufacturing.
The United States remains the dominant country in North America’s virus filtration market according to our global virus filtration market regional forecast, accounting for the majority of filter consumable revenues. Key factors include a dense network of contract development and manufacturing organizations (CDMOs), rapid approval cycles for biologics, and a mature regulatory framework enforced by the FDA. Recent development: In early 2025, the FDA released updated guidance clarifying validation requirements for virus removal filters in mRNA vaccine production, prompting manufacturers to upgrade to novel single-use filtration platforms to meet the new standards. This has accelerated procurement of advanced filter cartridges, reinforcing U.S. market leadership.
Canada is experiencing the fastest growth in North America’s virus filtration market, driven by government incentives aimed at expanding domestic biologics manufacturing capacity. A strong emphasis on pandemic preparedness has catalyzed facility expansions and the adoption of continuous bioprocessing platforms that integrate virus removal steps. Recent development: In March 2025, the Canadian government announced a CAD 150 million grant to foster biomanufacturing innovation, specifically earmarked for upgrading filtration workflows in emerging vaccine production facilities. This funding surge has led filter suppliers to establish localized warehouses, reducing lead times and further propelling Canada’s rapid growth trajectory.
Asia Pacific is the fastest growing region in the global virus filtration market, underpinned by massive investments in biopharmaceutical infrastructure across Japan, South Korea, and emerging Southeast Asian hubs. Rising demand for biologics, combined with government initiatives to bolster local vaccine manufacturing capabilities, has driven rapid adoption of advanced filtration systems. Japan and South Korea stand out due to their robust technology ecosystems, strong emphasis on innovation, and growing CDMO networks that cater to both regional and global clients. A focus on cost-effective, single-use technologies and continuous processing is gaining momentum, manufacturers in these countries are upgrading existing downstream lines to improve viral safety, throughput, and scalability. Moreover, favorable reimbursement policies and streamlined regulatory pathways for novel biologics amplify market potential. The convergence of AI-driven process analytics and high-capacity membrane platforms further accelerates growth; local filter developers collaborate with global partners to co-develop next-generation membranes that suit Asia Pacific production standards.
Japan commands the largest share of Asia Pacific’s virus filtration market, thanks to its advanced biotechnology sector and strong export orientation. The country’s major filter suppliers have long-established relationships with domestic biopharma companies, ensuring steady demand for consumables, instruments, and validation services. In February 2025, a prominent Japanese membrane manufacturer launched a new nanofiber virus-removal filter specifically optimized for continuous mAb processes, achieving a 30 percent increase in throughput during pilot testing. This innovation has quickly been adopted by leading CDMOs in Japan, cementing the country’s leadership in high-efficiency filtration technologies.
South Korea is growing at the fastest pace within the Asia Pacific virus filtration market, driven by an aggressive national biotech roadmap and substantial capital inflows into local biopharma startups. The government’s Biopharma 2030 initiative has provided dedicated funding for next-generation vaccine and gene therapy platforms, requiring stringent virus‐removal solutions. In April 2025, a leading South Korean CDMO partnered with a global filter technology provider to integrate AI-based membrane monitoring systems into its production lines, enabling real-time quality assurance and predictive maintenance. This alliance has reduced unplanned downtime by 25 percent and is forecast to boost filter consumable demand by 40 percent over the next two years.
Latin America is emerging in the global virus filtration market, fueled by expanding healthcare infrastructure, rising biologics production, and regulatory harmonization efforts. Brazil and Mexico are pioneering regional adoption, supported by government initiatives to improve vaccine self-sufficiency and upgrade downstream purification capabilities. The region faces challenges such as budget constraints and supply chain bottlenecks; however, increasing partnerships between local universities, contract service providers, and multinational filter suppliers are bridging technology gaps. Upgrades to quality control laboratories and growing focus on biosimilar manufacturing also contribute to the burgeoning need for virus removal systems in bioprocessing. As regulatory agencies in Latin America align more closely with international guidelines, demand for validated virus filtration workflows is projected to accelerate, making the region a strategic target for filter manufacturers aiming to penetrate new markets.
Brazil dominates Latin America’s virus filtration market, underpinned by its established vaccine and biosimilar manufacturing base. Major local players like Fundação Oswaldo Cruz (Fiocruz) and Bio-Manguinhos have invested in facility upgrades that incorporate state-of-the-art filtration trains for prophylactic vaccine production. Recent development: In January 2025, Fiocruz announced the commissioning of a new mRNA vaccine manufacturing plant equipped with advanced virus-removal membranes sourced from European and North American suppliers. This facility is expected to produce 100 million vaccine doses annually and has already begun validating filter performance under local regulatory scrutiny, marking a significant milestone in Brazil’s self-sufficiency strategy.
Mexico’s virus filtration segment is the fastest growing in Latin America, driven by an uptick in biopharma greenfield projects and expanding contract research services. Local biopharmaceutical firms are scaling up production of recombinant proteins and biosimilars, necessitating robust viral clearance steps. Recent development: In March 2025, the Mexican government approved a new biotech cluster in Querétaro, which includes a dedicated downstream processing center featuring modular, single-use virus filtration units. This center is slated to serve both local producers and export partners in South America, fueling a projected 50 percent increase in filter consumables demand by late 2026.
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Increased Demand for Biologics and Vaccines
Increasing Stringency of Regulatory Requirements
High Capital and Operating Costs
Technical Challenges and Supply Chain Issues
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The competitive landscape of the global virus filtration market is led by legacy bioprocessing giants like Merck KGaA, Sartorius AG, and Thermo Fisher Scientific, which leverage global virus filtration market strategies like acquisitions and new‐product launches (e.g., Merck’s Viresolve Prefilter Pods) to maintain market share. Sartorius focuses on single‐use, prevalidated membrane modules that shorten qualification timelines. Meanwhile, General Electric emphasizes strategic partnerships to co‐develop filtration systems tailored to novel biologics. A macro trend is the integration of real‐time monitoring and AI analytics into filtration workflows to predict membrane fouling and reduce downtime. The market remains moderately consolidated, but niche demands for high‐throughput, low‐fouling filters are driving targeted R&D investments and collaborations.
The global market is experiencing dynamic growth through the emergence of specialized startups which are forming special niches within the virus filtration market for global virus filtration market penetration. TeraPore Technologies leverages tunable block‐copolymer nanofiltration membranes (IsoBlock VF) that deliver uniform pore structures, enabling robust viral clearance even with challenging antibody formats. These startups occupy the high‐performance segment, forcing incumbents to accelerate membrane innovation and validation services while biosecurity startups expand testing ecosystems around filtration.
SkyQuest’s ABIRAW (Advanced Business Intelligence, Research & Analysis Wing) is our Business Information Services team that Collects, Collates, Correlates, and Analyses the Data collected by means of Primary Exploratory Research backed by robust Secondary Desk research.
As per SkyQuest analysis, the global virus filtration market is the increasing incidence of biologics and vaccines, a function of biopharmaceutical companies needing strong viral-clearance steps during production in order to demonstrate product purity and safety. However, high capital expenses and ongoing operational costs can be a challenge for new filtration systems and hold back growth of many independent fractionators, especially in developing markets.
The North America region is expected to dominate in the virus filtration space due to a mature biotech infrastructure, regulatory framework, and high research and development spending which will drive early adoption of next-generation filters. In this market segment, consumables are expected to dominate the market segment, and onwards revenues, the bulk of consumables revenues will derive from the use of single-use kits and membrane filters, because these are typically required as integral downstream processes, and ultimately, mirror the latency between biological pipelines maturing within individual organizations.
Report Metric | Details |
---|---|
Market size value in 2023 | USD 5.3 billion |
Market size value in 2032 | USD 12.81 billion |
Growth Rate | 10.3% |
Base year | 2024 |
Forecast period | 2025-2032 |
Forecast Unit (Value) | USD Billion |
Segments covered |
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Regions covered | North America (US, Canada), Europe (Germany, France, United Kingdom, Italy, Spain, Rest of Europe), Asia Pacific (China, India, Japan, Rest of Asia-Pacific), Latin America (Brazil, Rest of Latin America), Middle East & Africa (South Africa, GCC Countries, Rest of MEA) |
Companies covered |
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Customization scope | Free report customization with purchase. Customization includes:-
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Table Of Content
Executive Summary
Market overview
Parent Market Analysis
Market overview
Market size
KEY MARKET INSIGHTS
COVID IMPACT
MARKET DYNAMICS & OUTLOOK
Market Size by Region
KEY COMPANY PROFILES
Methodology
For the Virus Filtration Market, our research methodology involved a mixture of primary and secondary data sources. Key steps involved in the research process are listed below:
1. Information Procurement: This stage involved the procurement of Market data or related information via primary and secondary sources. The various secondary sources used included various company websites, annual reports, trade databases, and paid databases such as Hoover's, Bloomberg Business, Factiva, and Avention. Our team did 45 primary interactions Globally which included several stakeholders such as manufacturers, customers, key opinion leaders, etc. Overall, information procurement was one of the most extensive stages in our research process.
2. Information Analysis: This step involved triangulation of data through bottom-up and top-down approaches to estimate and validate the total size and future estimate of the Virus Filtration Market.
3. Report Formulation: The final step entailed the placement of data points in appropriate Market spaces in an attempt to deduce viable conclusions.
4. Validation & Publishing: Validation is the most important step in the process. Validation & re-validation via an intricately designed process helped us finalize data points to be used for final calculations. The final Market estimates and forecasts were then aligned and sent to our panel of industry experts for validation of data. Once the validation was done the report was sent to our Quality Assurance team to ensure adherence to style guides, consistency & design.
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With the given market data, our dedicated team of analysts can offer you the following customization options are available for the Virus Filtration Market:
Product Analysis: Product matrix, which offers a detailed comparison of the product portfolio of companies.
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Global Virus Filtration Market Size was valued at USD 4.6 billion in 2023 poised to grow from USD 5.16 billion in 2024 to USD 11.15 billion by 2032, growing at a CAGR of 10.10% during the forecast period (2025-2032).
The competitive landscape of the global virus filtration market is led by legacy bioprocessing giants like Merck KGaA, Sartorius AG, and Thermo Fisher Scientific, which leverage global virus filtration market strategies like acquisitions and new‐product launches (e.g., Merck’s Viresolve Prefilter Pods) to maintain market share. Sartorius focuses on single‐use, prevalidated membrane modules that shorten qualification timelines. Meanwhile, General Electric emphasizes strategic partnerships to co‐develop filtration systems tailored to novel biologics. A macro trend is the integration of real‐time monitoring and AI analytics into filtration workflows to predict membrane fouling and reduce downtime. The market remains moderately consolidated, but niche demands for high‐throughput, low‐fouling filters are driving targeted R&D investments and collaborations. 'Merck KGaA (Germany) ', 'Danaher Corporation (US) ', 'Sartorius AG (Germany) ', 'Thermo Fisher Scientific Inc. (US) ', 'General Electric Company (US) ', 'Lonza Group Ltd. (Switzerland) ', '3M Company (US) ', 'Pall Corporation (US) ', 'Wuxi Biologics (China) ', 'Clean Cell Inc. (US) ', 'Donaldson Company Inc. (US)', 'Veolia (France) ', 'Asahi Kasei Medical Co. Ltd. (Japan) ', 'Cytiva (US) ', 'TeraPore Technologies (US)'
With the shift towards biologic therapies and mRNA-based vaccines, the pressure to implement robust virus filtration has never been more pressing, which has evidently lead to global virus filtration market growth. As biopharmaceutical and biomanufacturing companies advance the development of new therapies like monoclonal antibodies, recombinant proteins, and gene therapy, they must establish and maintain viral safety throughout all stages of manufacture. The rapid growth in biologics pipelines has propelled the need for manufacturers to purchase effective virus-removal filters to comply with stringent purity regulations. As a result, the demand for virus filtration systems benefits from strong global growth in expanding biological production worldwide.
Move Towards Single-Use and Continuous Bioprocessing Platforms: Manufacturers are increasingly embracing single-use systems and continuous processing lines with integrated virus filtration for downstream purification, making up for another global virus filtration market trends. A single-use filter reduces opportunities for cross-contamination, minimizes subsequent change over time, and eliminates burdens for cleaning‐validation, making them particularly appealing for multiproduct facilities. Continuous bioprocessing extends productivity by facilitating uninterrupted viral‐clearance steps, which improves throughput while integrating sufficient viral safety. Additionally, the move to single-use processing systems supports flexibility objectives for facilities, because modular, disposable units can be quickly deployed or reconfigured to changing production capabilities while also flattening time-to-market.
How Does North America’s High Healthcare Expenditure Lead to Its Dominance in Global Virus Filtration Market?
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