Market Size (2021)
$27.75B
Vertical: HealthcareBase Year: 202112 Sections
Market Size (2021)
$27.75B
Projected (2030)
$59.12B
CAGR (2018–2030)
8.4%
Key Players
10+
The Global Plasma Fractionation Market is expected to register 8.9% CAGR during the forecast period, 2022 to 2030, and is expected to reach USD 59,115.9 million in 2030.
Global Plasma Fractionation Market is segmented based on product type, application, end user and region. Based on product type the market is segmented into Immunoglobulins, Coagulation Factor Concentrates, Albumin, Protease Inhibitors and Others. Based on Application the market is segmented into Immunology, Neurology, Hematology, Critical Care, Pulmonology, Rheumatology, Hemato-Oncology and Other. Based on end users, it is segmented into Hospitals & Clinics, Clinical Research Laboratories, Academic Institutes and Others Major regions considered within the market are North America, Europe, Asia Pacific, rest of the world.
The key players profiled in the global Plasma Fractionation analysis are CSL, Grifols Therapeutics, Baxter International Inc., Mitsubishi Tanabe, Kedrion S.p.A, and Takeda Pharmaceutical Company Limited and many more.
The major driver of the market's expansion is the growing prevalence of elderly people around the globe, who are more susceptible to rare disorders that call for the usage of blood derivatives. Additionally, the increased use of immunoglobulins & alpha-1-antitrypsin in various fields of medicine around the world is anticipated to drive market growth. Another important element driving the expansion of this market is the rise in blood collection facilities worldwide. Plasma fractionation has always ignited curiosity among researchers and industrialists alike. The therapeutic efficacies of blood plasma to treat and manage immunodeficiency diseases have helped the growth of the market. Cryo precipitation and ethanol fractionation are the major processes to separate therapeutic protein components from whole blood in the plasma fractionation equipment. Protein components, such as prothrombin complex, thrombin, fibrinogen, and others, play a major role in managing diseases. These fractionation plasma products have therapeutic efficiencies in treating diseases such as congenital metabolic deficiencies, trauma, immunological disorders, and other life-threatening diseases.
In response to the high demand for plasma-derived products, major companies in the market have engaged in several R&D initiatives to launch new plasma-derived therapies in the market. Furthermore, these key market players also intensely focused on owning and acquiring new plasma collection centres to streamline the availability of plasma to develop new products.
Increased investments by major players in the production of advanced & effective treatments are likely to support market growth throughout the projected timeframe. For instance, in April 2020, To create a viable plasma-derived medication for treating COVID-19, CSL Behring & Takeda Pharmaceutical Company Ltd. partnered with Biotest, BPL, LFB, and Octapharma. The collaboration will get started right away with the research and development of a single, unbranded anti-SARS-CoV-2 polyclonal hyperimmune immunoglobulin drug that has the potential to help people with major COVID-19 problems. Such initiatives by companies are likely to supplement the market growth in the coming years.
The Plasma Fractionation Market market is projected to grow at a CAGR of 8.4% from 2018 to 2030.
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View Subscription PlansPlasma Fractionation Market
Historical performance and future projections (2020–2030, USD Billion)
Market Size (USD Mn)
Blood plasma fractionation are the general processes of separating the various components of blood plasma, which in turn is a component of blood obtained through blood fractionation. Plasma-derived immunoglobulins are giving a new narrative to healthcare across a wide range of autoimmune inflammatory diseases.
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View Subscription PlansThis report applies a rigorous multi-stage research process combining primary interviews, secondary data sources, and bottom-up market modelling to ensure accuracy and completeness across all segments and geographies.
Base Year
2021
Historical Period
2018 – 2020
Forecast Period
2022 – 2030
Primary Interviews
150+
Historical data (2018–2021) and forecast period (2021–2030)
Our research process spans primary interviews with industry stakeholders combined with comprehensive secondary data analysis, validated through triangulation across multiple independent sources.
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View Subscription PlansThe global Plasma Fractionation market is profitable, both for existing players as well as new entrants. The market is highly competitive with all the players competing to gain a higher market share. Intense competition, rapid advances in Plasma Fractionation technology, and regulations are key factors that confront the market growth. A substantial level of rivalry is observed among the existing manufacturers in the market. Our analysis revealed that market players had adopted different strategies and innovative research and development techniques to expand their business and secure their position in the global Plasma Fractionation market. In recent years, strategic movements by major players included approvals, which have been used as market penetration strategies and a means to reduce competition. The key players profiled in the global Plasma Fractionation analysis are CSL, Grifols Therapeutics, Baxter International Inc., Mitsubishi Tanabe, Kedrion S.p.A, and Takeda Pharmaceutical Company Limited and many more. The industry is characterized by the presence of several small-scale industrial producers with obsolete production technologies and limited capacity, especially in developing nations, which has lent a significant advantage to new industry participants with better processing technologies.
Increased Investment by Major Players in Effective Treatment – For instance, CSL Behring & Takeda Pharmaceutical Company Ltd. collaborated with Biotest, BPL, LFB, and Octapharma to develop an effective plasma-derived drug for the treatment of COVID-19.
Europe and North America and are leading regions in geography size for plasma fractionation. This is mainly because majority of plasma is collected in over 450 collection centers in the U.S. and Europe. Large amounts of plasma products are exported from the U.S. and Europe to countries in Asia Pacific, South America, Middle East and Africa. The three dominating plasma fractionation companies in the world are CSL Behring, Grifols Therapeutics and Baxter Bioscience with a 75% of the market -roughly 25% or 10 million liters of yearly fractionation capacity for each one. These companies have a large product portfolio, a robust product pipeline, and an established global presence. The fractionation capacity of these three transnational players alone accounts for 30 million liters of plasma with an estimated capacity close to 40 million liters in 2024. A second tier of companies, including Octapharma, Kedrion, and Biotest account for a further 8 million liters of plasma fractionation capacity. Other companies such as BPL, Mitsubishi Tanabe, CBOP, RAAS, Hualan Bio and Sanquin also operate into the plasma fractionation business.
Key Players:
In 2021, CSL emerged as a dominant player in the plasma fractionation market, with a market share of 30-35%. The company has established a global presence by investing in capacity expansion, opening new centers, and maintaining a presence in over 35 countries with more than 230 plasma collection centres. CSL has also invested heavily in R&D to develop innovative biotherapies, with more than 1,700 employees dedicated to R&D activities. However, the company's involvement in legal proceedings and declining liquidity ratio could impede its growth, along with government regulations and unfavorable currency exchange rates.
Grifols accounted for a share of 15-20% of the plasma fractionation market in 2021, focusing on research, product innovation, expanding plasma collection centers, and increasing capacity. The company invests heavily in R&D and partners with research institutes to develop advanced plasma-derived products to fight rare diseases.
Shire accounted for a share of 11-16% of the plasma fractionation market in 2021, with expertise in medical devices, pharmaceuticals, and biotechnology. Takeda's acquisition of Shire helped the company gain a competitive edge in the market. BioLife, a part of Takeda, is a global plasma collection network that collects high-quality plasma.
Octapharma AG accounted for 8-12% of the plasma fractionation market in 2021, investing in research to advance existing products and investigate new therapeutic uses of human protein products derived from human blood plasma and human cell lines. The company focuses on organic and inorganic growth strategies and has received several approvals from various regulatory bodies.
Kedrion accounted for 2-5% of the plasma fractionation market in 2021, with a robust presence in around 100 countries across Asia, Europe, North America, and South America. The company strategically focuses on collaborations and agreements and collaborates with various hemophilia institutes to provide sustainable access to hemophilia treatment.
The global market for Plasma Fractionation is moderately competitive, owing to the presence of large regional and domestic players in different countries. Emphasis is given on the merger, expansion, acquisition, and partnership of the companies along with new product development as strategic approaches adopted by the leading companies to boost their brand presence among consumers.
Plasma fractionation is a critical process used to separate and purify various proteins and other components from plasma, which is the liquid portion of blood. The global plasma fractionation market has witnessed significant growth over the years, driven by factors such as an increase in the prevalence of chronic diseases, a growing aging population, and advancements in technology.
One major growth strategy in the global plasma fractionation market is the expansion of product portfolios. Key players in the market are continually investing in research and development to develop new and innovative products that meet the increasing demand for plasma-derived products. For instance, in recent years, there has been a surge in demand for immunoglobulin products due to their use in the treatment of various immunodeficiency disorders. As a result, several companies are investing in developing new immunoglobulin products to meet the growing demand.
Another growth strategy is the expansion of manufacturing capacities. The growing demand for plasma-derived products has resulted in an increased need for manufacturing facilities. Key players in the market are investing in building new manufacturing facilities and expanding existing ones to meet the growing demand. For example, in 2019, CSL Behring has announced plans for a 185-million-euro ($203 million) expansion in Marburg, Germany, where the global biotech already has its largest research and production facility. The expansion, expected to be completed in 2023, will support production of the company’s treatments for hereditary angioedema (HAE), a rare disease that causes dangerous swelling episodes.
Furthermore, mergers and acquisitions are also major growth strategies in the global plasma fractionation market. Companies are increasingly acquiring other companies to expand their product portfolios, gain access to new markets, and improve their competitive positions. For example, in 2021, Takeda Pharmaceutical acquired the plasma-derived therapy portfolio from Kamada Ltd. to strengthen its immunoglobulin portfolio.
In conclusion, the global plasma fractionation market is expected to continue to grow, driven by an increasing demand for plasma-derived products. Companies are expected to focus on expanding their product portfolios, expanding manufacturing capacities, and engaging in mergers and acquisitions to drive growth in the market.
For instance,
October 2022- Grifols inaugurated a new albumin purification and filling plant at its global manufacturing and supply hub in Dublin, Ireland.September 2022- CSL Behring K.K. received manufacturing and marketing approval from the Ministry of Health, Labour and Welfare of Japan for Berinert S.C. Injection 2000, a lyophilized human C1-esterase inhibitor concentrate for subcutaneous (SC) injection in plasma derivative, for the prevention of acute hereditary angioedema (HAE) attack.April 2020- Grifols launched 3- ml vial for Hyper RAB which is rabies immune globulin in the plasma fractionation market to help in the treatment of rabies cases across the world.March 2022- Grifols (Spain) received European approvals for XEMBIFY, a 20% subcutaneous immunoglobulin (SCIG)January 2022- Permira, a global investment firm, announced that it will be acquiring Kedrion and merging the company with BPL.August 2021- CSL (Australia) Received FDA approval for the new BERINERT [Cl Esterase inhibitor, Human (Intravenous)] Administration Kit for improved patient convenience.May 2022- in Douglas County, Colorado, Terumo Blood and Cell Technologies opened its newest production facility. The company's purpose of contributing to society via healthcare and serving more patients is aligned with the state-of-the-art production facility, which cost USD 250 million.
The 170,000-square-foot facility will produce single-use collection sets for the recent FDA-approved Rika Plasma Donation System to provide source plasma collections to clients (Rika).September 2019- Biopharma, a Ukraine based company which is specialized for the production plasma-based, recombinant and other drugs, launched a new plant for plasma fractionation in Bila Tserkva, Ukraine. The company offers a unique plasma fractionation technology which allows the plasma components of the blood to be processed for the extraction of life-saving drugs and the company is equipped with GMP — certified equipments and facilities. The launch of the company has put Ukraine almost on the same page as that of USA, Austria, and Germany. In the facility, production of blood products like Albumin, Bioven and Immunoglobulin is expected to help treat diseases caused due to immunodeficiency.
June 2019- Egypt initiated a project for the setup of the blood plasma fractionations and processing plant in the country in order to establish labs for the plasmapheresis.March 2021- according to the WHO Model List of essential medicines includes several plasma-derived medicinal products (PDMPs), identifying them as drugs thought to be the most efficient and secure for addressing the most essential requirements in a health system and provide the best guidelines on increased supply of PDMPs in low & middle-income countries.April 2020- to create a viable plasma-derived medication for treating COVID-19, CSL Behring & Takeda Pharmaceutical Company Ltd. collaborated with Biotest, BPL, LFB, and Octapharma.April 2019- under a long-term initiative to support people with hemophilia, Grifols International SA, a supplier of plasma-derived therapeutics, provided blood clotting factor medications (100 million international units) for the treatment of hemophilic patients.January 2022 - Octapharma AG announced that the European Union (EU) expanded the indication for cutaquig, a human immunoglobulin, administered subcutaneously. The expansion would provide more flexible treatment options to patients with acquired immune deficiencies.
January 2022 - Permira announced a partnership with the Marucci family and FSI, the existing shareholders of Kedrion S.p.A., to jointly acquire and combine Kedrion and Bio Products Laboratory (BPL). The two companies' partnership would create a global player for medicines derived from human plasma to treat life-threatening and rare conditions. January 2022- Kedrion S.p.A. and LFB formed an industrial cooperation agreement to increase the availability of immunoglobulins for patients in France. Following the agreement, immunoglobulins manufactured by Kedrion S.p.A will be imported by LFB in France and distributed among hospitals in this region along with their own immunoglobulins. January 2022- Bio Products Laboratory Ltd. announced that the National Medical Products Administration (NMPA) for China granted the company a license to market ALBUMINEX 25% in China. June 2021- LFB Plasma announced the acquisition of ImmunoTek Bio Center. The acquisition of the plasma collection center will ensure a steady and reliable supply of plasma in the U.S.December 2021- Grifols, S.A., through its Subsidiary company Grifols Canada Therapeutics Inc., acquired all the shares of Prometic Plasma Resources Inc.April 2021- CSL Plasma and Terumo Blood and Cell Technologies announced a collaboration to develop and deliver a new plasma collection platform at the U.S.
CSL Plasma Collection Centers.
Threat of New Entrants
The plasma fractionation industry requires significant investment in research and development, manufacturing, and regulatory compliance. This high barrier to entry limits the threat of new entrants. In addition, there are few new sources of plasma that can compete with existing suppliers, which further reduces the threat of new entrants. Moreover, the plasma fractionation industry is dominated by a few large players that have economies of scale and established relationships with suppliers and customers. These factors create significant advantages for existing companies and make it difficult for new entrants to gain a foothold in the market. Another factor that reduces the threat of new entrants is the limited availability of plasma sources. Plasma is primarily obtained from human donors, and there are relatively few new sources of plasma that can compete with existing suppliers. This means that existing companies have an advantage in terms of securing a reliable and consistent supply of plasma, which is critical for manufacturing plasma-derived products.
Hence, the threat of new entrants in the Global Plasma Fractionation Market is expected to be high.
Bargaining Power of Suppliers
The bargaining power of suppliers in the plasma fractionation industry is significant due to the limited number of suppliers of high-quality plasma. Plasma is the primary input for the industry, and the quality of the plasma has a direct impact on the quality of the final products.
The limited number of plasma suppliers gives these suppliers significant bargaining power over plasma fractionation companies. Suppliers can use this power to negotiate higher prices for their plasma or to set strict quality standards for the plasma they provide.
However, plasma fractionation companies can mitigate the bargaining power of suppliers in several ways. One approach is to form long-term relationships with suppliers. By establishing long-term relationships, plasma fractionation companies can gain greater control over their supply chain and build trust with suppliers. This can lead to more favorable pricing and quality terms over time. Another approach is for plasma fractionation companies to invest in plasma collection centers. By doing so, they can increase their control over the supply of plasma and reduce their dependence on external suppliers. This approach can also help plasma fractionation companies to ensure the quality of the plasma they use in their manufacturing processes.
Finally, plasma fractionation companies can consider acquiring suppliers. By acquiring suppliers, plasma fractionation companies can gain greater control over the supply of plasma and reduce their dependence on external suppliers. This approach can also help to ensure the quality of the plasma used in the manufacturing process and provide a more stable supply of plasma over time.
Overall, while the bargaining power of suppliers in the plasma fractionation industry is significant, plasma fractionation companies can mitigate this power by forming long-term relationships with suppliers, investing in plasma collection centers, or acquiring suppliers. These approaches can help to ensure a stable supply of high-quality plasma at favorable pricing and quality terms.
Hence, the bargaining power of suppliers in the Global Plasma Fractionation Market is expected to be low.
Threat of Substitutes
The threat of substitutes in the plasma fractionation industry is relatively low due to the limited number of substitutes available for plasma-derived products, particularly for patients with rare diseases. However, advances in gene therapy and other biotechnologies may create substitutes for some plasma fractionation products in the future.
The success of these new technologies will determine the extent of the threat posed by substitutes to the plasma fractionation industry. If these new technologies are successful, they may create viable substitutes for some plasma-derived products, particularly those used to treat rare diseases. This could reduce the demand for some plasma fractionation products and potentially impact the profitability of plasma fractionation companies.
The cost and effectiveness of substitutes will also play a significant role in determining the threat they pose to the plasma fractionation industry. If substitutes are more cost-effective and equally or more effective than existing plasma-derived products, they may gain market share and reduce the demand for plasma fractionation products.
However, it is worth noting that the development and commercialization of new technologies can be a lengthy and challenging process, particularly in the highly regulated healthcare industry. Additionally, plasma fractionation companies have significant expertise in manufacturing and distributing plasma-derived products, and this expertise could help them to adapt to new technologies and maintain their market position.
Overall, while the threat of substitutes to the plasma fractionation industry is currently low, advances in gene therapy and other biotechnologies may create viable substitutes for some plasma-derived products in the future. The extent of this threat will depend on the success of these new technologies and the cost and effectiveness of substitutes compared to existing plasma fractionation products.
Hence, the threat of substitutes in the Global Plasma Fractionation Market is expected to be moderate.
Bargaining Power of Buyers
The bargaining power of buyers in the plasma fractionation industry is significant due to the large volume of products they purchase and the importance of these products in patient care. Hospitals, clinics, and other healthcare providers that buy plasma fractionation products have significant negotiating power over plasma fractionation companies.
However, the specialized nature of plasma fractionation products and the limited number of suppliers somewhat limit the bargaining power of buyers. Plasma fractionation products are highly specialized, and many of them are used to treat rare diseases. As a result, buyers may have limited options when it comes to sourcing these products, which can reduce their bargaining power. The limited number of suppliers in the plasma fractionation industry also limits the bargaining power of buyers. There are only a few companies that specialize in plasma fractionation, which can make it difficult for buyers to find alternative suppliers.
Despite these limitations, buyers still have significant bargaining power in the plasma fractionation industry. To mitigate the bargaining power of buyers, plasma fractionation companies may offer volume discounts or other incentives to encourage buyers to purchase their products. Additionally, plasma fractionation companies may invest in research and development to create new products that can differentiate them from competitors and give them more negotiating power with buyers.
Overall, while the bargaining power of buyers in the plasma fractionation industry is significant, the specialized nature of plasma fractionation products and the limited number of suppliers somewhat limit the bargaining power of buyers. Plasma fractionation companies can mitigate this power by offering incentives to buyers and investing in research and development to create new products that differentiate them from competitors.
Hence, the bargaining power of buyers in the Global Plasma Fractionation Market is expected to be high.
Intensity of Rivalry
The plasma fractionation industry is dominated by a small number of large companies, which creates intense rivalry among competitors. The key areas of competition among plasma fractionation companies include product development, pricing, and marketing. In product development, companies strive to create new and innovative plasma-derived products to meet the needs of patients with rare diseases and other medical conditions. This can be a costly and time-consuming process, but it is necessary to remain competitive in the industry.
Pricing is another area of intense competition in the plasma fractionation industry. Companies must balance the need to generate revenue with the need to make their products affordable for patients and healthcare providers. Pricing decisions can have a significant impact on market share and profitability.
Marketing is also a critical area of competition in the plasma fractionation industry. Companies must differentiate themselves from competitors and promote their products to healthcare providers and patients. Effective marketing can help to build brand awareness and increase market share.
Despite the intense rivalry among existing competitors, the high barriers to entry and the specialized nature of the industry limit the number of competitors and the intensity of competition to some extent. The significant investment required for research and development, manufacturing, and regulatory compliance makes it difficult for new entrants to enter the industry. The specialized nature of the plasma fractionation products also limits the number of companies that can effectively compete in the industry.
Overall, while the plasma fractionation industry is characterized by intense rivalry among existing competitors, the high barriers to entry and the specialized nature of the industry limit the number of competitors and the intensity of competition to some extent. Companies must continue to invest in product development, pricing, and marketing to remain competitive in the industry.
Hence, the intensity of rivalry in the Global Plasma Fractionation Market is expected to be moderate.
Market estimates by geography (2030)
InsightNorth America leads with $30.29B by 2030, while Asia Pacific is projected to grow fastest at a 9.4% CAGR.
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View Subscription Plans| REGION | 2018 | 2021 | 2030 | CAGR | SHARE |
|---|---|---|---|---|---|
| North America | $12.10B | $18.30B | $30.29B | 8.0% | 51% |
| Europe | $4.52B | $7.10B | $12.22B | 8.6% | 21% |
| Asia Pacific | $5.11B | $8.33B | $14.93B | 9.4% | 25% |
| Rest of the World | $727.73M | $1.05B | $1.67B | 7.2% | 3% |
| Total | $22.45B | $34.78B | $59.12B | 8.4% | 100% |
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View Subscription PlansTotal Market Size
$59.12B
| APPLICATION | REVENUE ($B) | GROWTH RATE | MARKET PENETRATION |
|---|---|---|---|
| Immunoglobulin | $33.49B | 8.2% | 57% |
| Coagulation Factor Concentrates | $10.28B | 9.1% | 17% |
| Albumin | $7.30B | 9.8% | 12% |
| Protease Inhibitors | $6.85B | 7.4% | 12% |
| Others | $1.19B | 7.3% | 2% |
* Revenue projections based on 2025 estimates. Growth rates represent CAGR 2024–2030. Market penetration indicates current adoption rate within addressable market segments.
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Analytical insights on Plasma Fractionation Market covering market dynamics, competitive landscape, and strategic outlook.
The Plasma Fractionation Market market is projected to reach $59.12B by 2030, growing at 8.4% CAGR. The Immunoglobulin segment holds the largest share.
Immunoglobulins are used as first-line therapy for various neurologic, immunologic, and hematologic conditions. In the last decade, the diagnosis rate of various immunological diseases has increased due to technological advancements. Growing genetic research for characterizing and diagnosing immunodeficiency will also increase the clinical need for immunoglobulins due to the increased number of diagnosed patients. According to IG Living, a magazine for the immune globulin (IG) community, there are several on- and off-label indications of IVIg. In recent years, the use of off-label indications of immunoglobulin has exceeded that of on-label indications; off-label indications of immunoglobulin account for around 20—60% of its clinical use.
The use of immunoglobulin in treating various disorders, including primary and secondary immune deficiencies, autoimmune diseases, and inflammatory diseases, is driving the growth of this market segment. A study published in May 2022 revealed that intravenous immunoglobulin (IVIG) was among the top three most used monotherapy for livedoid vasculopathy (LV), a rare disease, and is a safe and effective treatment.
The prevalence of rare and autoimmune diseases and an increase in immunology research worldwide are further driving the growth of this segment. According to data published by the National Center for Advancing Translational Sciences in February 2022, there are approximately 7,000 to 10,000 rare diseases affecting humans, of which only a few hundred have any treatment. The rising number of rare diseases is contributing to the growth of the immunoglobulin market segment.
Similarly, the incidence of autoimmune diseases is also increasing, as evidenced by a research study published in January 2022 that highlighted the prevalence of Acquired hemophilia A (AHA), a rare bleeding disorder. The growing prevalence of autoimmune diseases is expected to drive the demand for immunoglobulin-based treatment, further boosting the plasma fractionation market.
Market players are focusing on developing innovative drugs and exploring new therapeutic areas for existing drugs to stay competitive. For instance, Sanofi and IGM Biosciences, Inc. announced a collaboration in March 2022 to develop immunoglobulin antibody agonists for three oncology and immunology/inflammation targets. The rising research and development activity on immunoglobulins is expected to continue to propel the growth of this market segment.
This process involves breaking down plasma into various individual proteins, such as albumin, immunoglobulin and coagulation factor, and protease inhibitor, for clinical use. Major key players in this market have their own plasma fractionation centers where they can extract such proteins. The current demand for plasma-derived therapies led to the launch of various technologies which can make the process faster. For instance, in April 2021, GEA delivered a new separator technology to Biopharma S.A. in its new plant in Bila Tserkva, Ukraine. In March 2022, the U.S. Food and Drug Administration also cleared Terumo Corporation’s BCT collection system to meet the increasing demand for plasma-derived therapies. Rika Plasma Donation System is said to be a next-generation automated technology designed to meet the growing demand for plasma-derived therapies. On average, the device can complete plasma collection within 35 minutes, ensuring that at one time, there is not more than 200 milliliters of blood outside the donor’s body. The continuous efforts by various players to introduce technologies for the plasma fractionation process will augment the growth opportunities for the market over the forecast period.
In recent years, many recombinant alternatives have been developed for various plasma-driven therapies. Recombinant products are used prophylactically and are comparatively less immunogenic than plasma-derived products. In addition to these, various other longer-acting replacement factors are in the development pipeline. The products provide significant benefits, like less frequent administration, and are more effective in prophylactic use. The growing use of recombinant factors and their increased use in prophylactic therapies is thus a major factor limiting the adoption of plasma products. The recombinant product version of plasma-derived products is manufactured by the expression of equivalent proteins from genetically engineered cells and offers a safer option than plasma-derived products as they avoid potential blood-borne transmission of infectious diseases. Therefore, the advantages associated with such products make them more reliable than plasma-derived products, thus restraining the market growth. Recent approvals for recombinant factors, such as AFSTYLA (CSL), VONVENDI (Takeda/Shire), and Kovaltry (Bayer), are expected to provide profitable opportunities for companies in the market space. Two classes of recombinant factor products are currently available, standard half-life products and extended half-life products.
In developed countries, recombinant factors Vlll and IX have gained traction as alternatives to plasma-derived factors in bleeding disorders, according to the World Federation of Hemophilia's Annual Global Survey conducted in 2020. The use of recombinant factors has also increased in countries such as Brazil, India, and Russia. This trend is likely to limit the expansion of plasma-derived coagulation factors, thereby affecting overall market growth.
The COVID-19 outbreak led to various organizations experimenting with plasma-based therapies for the treatment of infected individuals. Several companies launched various research & development initiatives to combat COVID-19. For instance, in 2020, Biotest AG entered into industry-wide cooperation within the COVID-19 Plasma Alliance along with companies such as LFB, CSL Behring, Takeda Pharmaceutical Company Limited, and Octapharma AG. The companies together worked on a new polyclonal hyperimmunoglobulin drug against SARS-CoV-2. However, the market experienced slow growth due to the disruption in the plasma collection process. Despite being called an “essential infrastructure”, plasma collection was impacted due to the growth in the number of cases and COVID-19 guidelines such as social distancing and stay-at-home orders. For example, according to the annual report published by CSL Limited for the year 2020/2021, due to COVID-19, the plasma collection volume decreased along with an increase in the cost of collection with respect to donor compensation. Furthermore, the revenues for major companies were also impacted. For example, Octapharma AG recorded a growth of 8.1% in its revenue in FY 2020 compared to 23.2% in 2019. Similarly, Grifols, S.A. also witnessed a slow growth of 4.8% in 2020 compared to 15.6% in 2019 in the segments of biosciences and bio supplies.
Plasma fractionation is a process of separating various components of blood plasma to produce products such as immunoglobulins, clotting factors, albumin, and other specialty products for use in treating a variety of medical conditions. The COVID-19 pandemic has had a significant impact on the global supply chain for plasma fractionation, affecting both the demand and supply of plasma-derived products.
Demand for plasma-derived products has increased significantly due to the COVID-19 pandemic, particularly for critical care patients, including those with severe respiratory distress syndrome caused by COVID-19. This has put pressure on the supply chain to meet the increased demand for plasma-derived products. At the same time, the COVID-19 pandemic has disrupted the global supply chain for plasma fractionation. The pandemic has led to travel restrictions, social distancing requirements, and temporary closures of many plasma collection centers. This has resulted in a reduction in the supply of plasma, making it difficult for plasma fractionation companies to meet the increased demand for plasma-derived products.
Additionally, the pandemic has led to disruptions in transportation and logistics, making it difficult to transport plasma from collection centers to fractionation facilities and finished products to end-users. This has caused delays in the delivery of plasma-derived products to patients who depend on them for treatment. To address these challenges, many plasma fractionation companies have taken steps to mitigate the impact of the pandemic on the supply chain. These include implementing new safety protocols at collection centres, developing new partnerships with plasma collectors, and investing in new technologies to improve the efficiency of the fractionation process.
In summary, the COVID-19 pandemic has had a significant impact on the global supply chain for plasma fractionation. While the increased demand for plasma-derived products has put pressure on the supply chain, disruptions to the plasma collection and transportation process have made it challenging for fractionation companies to meet this demand. Despite these challenges, many companies have adapted to the changing circumstances and are taking steps to improve the efficiency and resilience of the plasma fractionation supply chain.
The COVID-19 pandemic has had a significant impact on the production of plasma fractionation, which is the process of separating plasma into its components, including immunoglobulins, albumin, and clotting factors. Plasma-derived products are crucial for treating a wide range of medical conditions, including immune deficiencies, bleeding disorders, and neurological diseases. The COVID-19 pandemic has increased the demand for plasma-derived products, particularly for the treatment of severe COVID-19 patients. The plasma of individuals who have recovered from COVID-19 contains antibodies against the virus, which can be used to treat critically ill patients. This has led to an increase in demand for plasma donation, but also to challenges in maintaining the supply chain of plasma-derived products.
Lockdowns and social distancing measures have led to a decrease in the number of plasma donors, as people are unable or unwilling to donate due to fear of exposure to the virus. This has resulted in shortages of plasma-derived products in some regions, leading to rationing and prioritization of treatments.
The pandemic has also disrupted the supply chain for plasma-derived products, as transportation and logistics have been affected by restrictions and closures of borders and airports. This has led to delays in the delivery of these products to patients, further exacerbating the shortage of supply.
To address these challenges, plasma fractionation companies have implemented measures to ensure the safety of their employees and donors, including increased use of personal protective equipment, social distancing, and enhanced cleaning protocols. They have also ramped up plasma collection efforts, including the use of mobile donation centers and the recruitment of convalescent plasma donors.
Overall, the COVID-19 pandemic has had a significant impact on the production of plasma fractionation, leading to challenges in maintaining the supply chain of plasma-derived products. However, efforts are being made to address these challenges and ensure that patients continue to have access to these life-saving treatments.
Plasma fractionation is a critical process that involves the separation of blood plasma into its different components, such as immunoglobulins, albumin, and clotting factors. These components are then used to produce a range of life-saving medicines, including immune globulins, coagulation factors, and albumin. The COVID-19 pandemic has had a significant impact on the demand for plasma-derived products, particularly immune globulins. Immune globulins are used to treat a variety of medical conditions, including immune deficiencies and autoimmune disorders. However, during the pandemic, immune globulins were also used to treat COVID-19 patients, particularly those with severe symptoms.
The demand for immune globulins skyrocketed during the pandemic, which led to a shortage of plasma-derived products in some regions. This shortage was primarily due to the closure of plasma collection centres in many countries, as well as the reduction in donor visits due to restrictions and fears related to the pandemic.
The impact of COVID-19 on plasma fractionation varied by region. In North America, for example, the demand for plasma-derived products increased significantly during the pandemic, and the supply chain was disrupted due to the closure of plasma collection centres. This led to a shortage of immune globulins, which affected patients with immune deficiencies and autoimmune disorders.
In Europe, the impact of COVID-19 on plasma fractionation was also significant. The pandemic caused a decrease in the number of plasma donations, which led to a reduction in the supply of plasma-derived products. This shortage was further compounded by the increased demand for immune globulins to treat COVID-19 patients.
In Asia-Pacific, the impact of COVID-19 on plasma fractionation was less severe than in North America and Europe. This was due to the fact that many countries in the region were able to maintain their plasma collection centres and supply chains, despite the pandemic. Overall, the COVID-19 pandemic had a significant impact on plasma fractionation and the supply of plasma-derived products. However, the exact impact varied by region, depending on factors such as the number of plasma collection centres, the availability of donors, and the demand for plasma-derived products.
Plasma fractionation is the process of separating blood plasma into its individual components, such as proteins and antibodies, for use in medical treatments. During the COVID-19 pandemic, plasma fractionation has played a critical role in the development of treatments for the virus. As the demand for COVID-19 treatments has increased, so has the demand for plasma fractionation. This has resulted in a significant supply-demand gap for plasma-based products, including convalescent plasma and immunoglobulins.
To address this gap, many countries have implemented measures to increase plasma collection, such as encouraging recovered COVID-19 patients to donate their plasma and offering financial incentives to plasma donors. Additionally, some companies have expanded their production of plasma-based treatments to meet the increased demand.
However, despite these efforts, the supply-demand gap for plasma-based products remains a challenge. The high demand for convalescent plasma, which contains antibodies from recovered COVID-19 patients, has led to shortages in some regions. In addition, the production of plasma-based treatments can be time-consuming and complex, which further limits the supply.
Overall, the impact of COVID-19 on plasma fractionation has highlighted the importance of maintaining a stable and sustainable supply of plasma-based products. It has also underscored the need for continued investment in plasma collection and production to ensure that adequate supplies are available for future pandemics or other healthcare crises.
The COVID-19 pandemic has had a significant impact on the plasma fractionation industry, including its pricing. One of the main impacts of the pandemic has been an increase in demand for plasma-derived products such as immunoglobulins, which are used to treat patients with severe COVID-19 infections.
The increased demand for immunoglobulins and other plasma-derived products has led to a rise in their prices. This increase in pricing has been driven by several factors, including increased demand, disruptions in the supply chain, and production challenges caused by the pandemic.
The pandemic has also created uncertainty in the plasma fractionation industry, which has made pricing more challenging. The industry is highly regulated, and pricing decisions must take into account a range of factors, including manufacturing costs, regulatory compliance, and market demand.
Additionally, the pandemic has created economic challenges for patients and healthcare providers, which has put pressure on plasma fractionation companies to keep their prices affordable. Many companies have responded by offering discounts and other incentives to patients and healthcare providers.
In summary, the COVID-19 pandemic has had a significant impact on the pricing of plasma-derived products, particularly immunoglobulins. The increase in demand for these products has led to a rise in their prices, but companies are also facing pressure to keep their prices affordable in the face of economic uncertainty. The industry must balance these competing factors to ensure that patients have access to the plasma-derived products they need to treat a range of medical conditions.
Profiles of 105 companies operating in the Plasma Fractionation Market market, including revenue, employee count, and market positioning where available.
Showing 105 of 105 companies
Biotest AG
Company Headquarters: Germany Founded: 1946 Workforce: ~ 1,959 Company Working: Biotest AG is a Germany-based provider of plasma proteins and biological drugs. The Company, with a chain that extends from pre-clinical and clinical development to worldwide marketing and distribution, mainly specializes in the areas of clinical immunology, hematology, and intensive care medicine. Biotest AG develops, manufactures, and markets immunoglobulin, coagulation factors and albumins based on human blood plasma. These are used for diseases of the immune and hematopoietic systems. In addition, the Company develops monoclonal antibodies in the indications of cancer of plasma cells and systemic lupus erythematosus, which are produced by recombinant technologies. Barcelona-based Grifols, a global leader in plasma-derived medicines, today announced the completion of the acquisition of Biotest AG, a European healthcare company specialized in innovative hematology and clinical immunology.
Kedrion S.p.A.
Company Headquarters: Italy Founded: 2000 Workforce: ~1,050 Company Working: Kedrion S.p.A. develops and distributes plasma-derived medicinal products. The Company produces plasma-derived products for use in treating serious diseases, disorders, and conditions such as hemophilia and immune system deficiencies. Kedrion serves customers worldwide. Kedrion is a biopharmaceutical company that specializes in the development, production, and distribution of plasma-derived therapeutic products for use in treating serious diseases, disorders, and conditions such as immune system deficiencies and coagulation disorders. The company operates through a fully integrated business model from the collection of plasma in its own centres in the United States to fractionation and production in its manufacturing facilities located in Italy, Hungary, and North America. Headquartered in Castelvecchio Pascoli (Lucca, Italy), Kedrion has approximately 2,800 employees and a commercial presence in 100 countries worldwide.
Grifols Therapeutics
Company Headquarters: Spain Founded: 1909 Workforce: ~ 4,763 Company Working: Grifols Therapeutics, Inc. operates as a biotherapeutic and biotechnology company. The Company discovers, develops, and produces critical care treatment products for the people with life-threatening disorders. Grifols Therapeutics serves patients, hospitals, pharmacies, and healthcare professionals worldwide. Grifols SA is a Spain-based global specialty pharmaceutical company developing, manufacturing, and distributing a broad range of biological medicines based on plasma derived proteins. It organizes its business into five divisions: Bioscience, Diagnostic, Hospital, Bio Supplies and Others. Bioscience includes manufacturing activities of plasma derivatives for therapeutic use and the sale and distribution of end products. Diagnostic focuses on researching, developing, manufacturing, and marketing in vitro diagnostics products, such as analytical instruments, reagents and software, among others, for laboratories. Hospital offers technology and services for hospitals, clinics and specialized centers for the manufacture of medicines, as well as physiological saline solution, enteral nutritional fluids and medical devices for interventional therapy. Bio Supplies provides, mostly, biological products for non-therapeutic use. Others provides manufacturing services to third party companies. Grifols' plasma fractionation capacity is 3.6 million liters of plasma a year and is carried out in the company's two plants located in Parets del Valles (Barcelona) and Los Angeles.
CSL Behring
Company Headquarters: USA Founded: 2000 Workforce: ~27,000 Revenue: USD 10.56 Billion (December 31, 2021) Company Working: CSL Behring is a biopharmaceutical company, manufacturing plasma-derived, and recombination therapeutic products. Its line of therapies includes products for the treatment of bleeding disorders such as hemophilia; hereditary angioedema; inherited respiratory disease; and neurological disorders. CSL Behring is focused on serving patients with serious and rare diseases, including coagulation disorders, primary immune deficiencies, hereditary angioedema, respiratory disease and neurological disorders. Company collaborates with patient and biomedical communities to improve access to therapies, advance scientific knowledge and support future medical research. CSL Behring's dynamic environment fosters innovation and attracts the best and brightest who share a commitment to helping save lives. CSL Behring is committed to diversity and inclusion, both of which underpin our Values of patient focus, innovation, collaboration, integrity, and superior performance. CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. The parent company, CSL Limited, headquartered in Melbourne, Australia, employs more than 27,000 people, and provides its life-saving medicines in more than 70 countries. CSL Limited is the parent company of global biotechnology leader CSL Behring; the world's largest collector of human plasma, CSL Plasma; and global leader in influenza prevention, Seqirus. CSL Limited is based in Melbourne, Victoria, Australia, and is traded on the Australian Securities Exchange (ASX) under the symbol CSL.
Mitsubishi Tanabe Pharma
Company Headquarters: Japan Founded: 1678 Workforce: ~ 69,784 Revenue: USD 34.64 Billion Company Working: Mitsubishi Tanabe Pharma Corp (Mitsubishi Tanabe), a subsidiary of Mitsubishi Chemical Holdings Corp, identifies, develops, manufactures, procures, and commercializes ethical drugs and over the counter (OTC) pharmaceutical products. The company develops ethical drugs for autoimmune disease, diabetes, kidney diseases, central nervous system (CNS) disorders, and others. It also develops vaccines for preventing various infectious diseases. Mitsubishi Tanabe also offers major products for skin conditions and digestive medicines. The company markets its products to wholesalers, hospitals, clinics, and drugstores. It has subsidiaries in Asia, Europe, and North America. Mitsubishi Tanabe is headquartered in Osaka, Japan.
Hualan Biological Engineering Inc.
Company Headquarters: China Founded: 1992 Workforce: ~ 2,927 Company Working: Hualan is a pharmaceutical firm specializing in the production of direct or indirect contact injection pharmaceutical packaging materials. Hualan Biological Engineering Inc. (Hualan Bio) is a key National high-tech biopharmaceutical company in China engaging in the research, development, production, and commercialization of plasma products, viral vaccines, bacterial vaccines, and recombinant proteins and other biologics. Hualan Bio was the first company whose plasma products gained GMP certificate in China, the first listed company of plasma products, the first H1N1 Influenza Vaccine manufacturer in the whole world, the first influenza vaccine manufacturer passing WHO-PQ in China. Passing "ISO9000" (quality), "ISO14000" (environment) and "GBT28000" (occupational health) management system certification. As a major manufacturer for the plasma products and vaccines designated by national authorities, Hualan Bio is the largest manufacturer and provider for both plasma products and influenza vaccines in Asia. Hualan Bio is the leading company which has integrated the innovative R & D activities, state-of the-art technologies, scientific management styles and high standard quality control and assurance systems in China. The company has been undertaking research projects from national, provincial, and municipal organizations. In 2010, Hualan Bio formed a strategic alliance with the Chinese Academy of Sciences (CAS) and collaborates with several institutes for the discovery of innovative biologics. Recently, the R & D center at Hualan Bio was recognized as one of the National High-tech Center in China, which built the solid foundation for the development of novel products and future growth.
12 interactive charts drawn from the Plasma Fractionation Market dataset — market size, regional splits and each segment breakdown. Open one to read its full data table and download it.
Global Plasma Fractionation Market By End User Others Parent
Global Plasma Fractionation Market By End User
Global Plasma Fractionation Market By Application
Global Plasma Fractionation Market By Product Type
Global Plasma Fractionation Market Latin-America, Middle-East and Africa Of Rest Of The World
Global Plasma Fractionation Market China, Japan, India, Australia, South Korea and Rest Of Asia Pacific By Country
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