#Cell and Gene Therapy Manufacturing Services Market Size

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The Cell and Gene Therapy Manufacturing Services Market in 2023 is US$ 6 billion, and is expected to reach US$ 22.14 billion by 2031 at a CAGR of 17.70%.

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Cell & Gene Therapy Manufacturing Services Market: Growth Opportunities for New Entrants

The global Cell & Gene Therapy Manufacturing Services Market is experiencing significant growth, driven by advancements in therapeutic approaches for life-threatening and rare diseases. Valued at USD 11.4 billion in 2023, the market is projected to reach USD 70.7 billion by 2032, exhibiting a compound annual growth rate (CAGR) of 22.4% over the forecast period 2024-2032.

Market Segmentation:

The market is segmented based on therapy type, manufacturing scale, manufacturing mode, workflow, and region.

By Therapy Type:

Cell Therapy Manufacturing

Gene Therapy Manufacturing

By Manufacturing Scale:

Preclinical

Clinical

Commercial

By Manufacturing Mode:

In-House Manufacturing

Contract Manufacturing

By Workflow:

Vector Production

Cell Banking

Process Development

Fill & Finish Operations

Analytical & Quality Testing

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Regional Analysis:

North America: Leading the market due to substantial investments in gene therapy companies and a high number of ongoing clinical trials.

Europe: Experiencing growth driven by increased R&D activities and supportive regulatory frameworks.

Asia-Pacific: Anticipated to witness rapid growth owing to rising prevalence of target diseases and expanding healthcare infrastructure.

Key Players

Cellular Therapeutics

Lonza

Bluebird Bio Inc.

Thermo Fisher Scientific

Samsung Biologics

Boehringer Ingelheim

Hitachi Chemical Co., Ltd.

Takara Bio Inc.

Catalent Inc.

Miltenyi Biotec

F. Hoffmann-La Roche Ltd

Novartis AG

Merck KGaA

Wuxi Advanced Therapies and others.

Key Highlights:

As of May 2022, there were 329 cell and gene therapies undergoing clinical trials, with numbers expected to rise due to improved scientific understanding and clinical practices.

Approximately USD 2.3 billion has been invested in gene therapy companies over the past decade, indicating strong commitment from global pharmaceutical and biotechnology firms.

The increasing prevalence of cancer and other target diseases, along with heightened R&D spending by pharmaceutical companies, is propelling market growth.

Future Outlook:

The Cell & Gene Therapy Manufacturing Services Market is poised for substantial expansion, driven by the rising incidence of diseases such as cancer and orthopedic disorders, which necessitate innovative treatment solutions. The establishment of new manufacturing facilities and advancements in therapeutic approaches are expected to further fuel market growth. However, challenges such as high operational costs and the need for specialized infrastructure may impact the pace of expansion.

Conclusion:

The global Cell & Gene Therapy Manufacturing Services Market is on a robust growth trajectory, with significant developments across various segments and regions. Stakeholders, including manufacturers, healthcare providers, and investors, are well-positioned to benefit from the evolving landscape of cell and gene therapy manufacturing services.

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Biobanking: An Overview of Its Role in Modern Medical Research

The global biobanking market size is expected to reach USD 67.90 Billion in 2030 and register a revenue CAGR of 8.6% over the forecast period, according to latest analysis by Emergen Research. Increasing genomic research activities and investment in R&D by major companies is driving global biobanking market revenue growth. Surge in research activities of regenerative medicines, stem cell therapeutics, and cell and gene therapy is also driving revenue growth of the global market.

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Competitive Terrain:

The global Biobanking industry is highly consolidated owing to the presence of renowned companies operating across several international and local segments of the market. These players dominate the industry in terms of their strong geographical reach and a large number of production facilities. The companies are intensely competitive against one another and excel in their individual technological capabilities, as well as product development, innovation, and product pricing strategies.

The leading market contenders listed in the report are:

U.K. Biobank Limited, Medizinische Universitat Graz, Hamilton Company, ASKION, Azenta Life Sciences, Qiagen, Promega Corporation, Integrated Biobank of Luxembourg (IBBL), Isenet Biobanking and Thermo Fisher Scientific, Inc

Key market aspects studied in the report:

Market Scope: The report explains the scope of various commercial possibilities in the global Biobanking market over the upcoming years. The estimated revenue build-up over the forecast years has been included in the report. The report analyzes the key market segments and sub-segments and provides deep insights into the market to assist readers with the formulation of lucrative strategies for business expansion.

Competitive Outlook: The leading companies operating in the Biobanking market have been enumerated in this report. This section of the report lays emphasis on the geographical reach and production facilities of these companies. To get ahead of their rivals, the leading players are focusing more on offering products at competitive prices, according to our analysts.

Report Objective: The primary objective of this report is to provide the manufacturers, distributors, suppliers, and buyers engaged in this sector with access to a deeper and improved understanding of the global Biobanking market.

Emergen Research is Offering Limited Time Discount (Grab a Copy at Discounted Price Now)@ https://www.emergenresearch.com/request-discount/926

Market Segmentations of the Biobanking Market

This market is segmented based on Types, Applications, and Regions. The growth of each segment provides accurate forecasts related to production and sales by Types and Applications, in terms of volume and value for the period between 2022 and 2030. This analysis can help readers looking to expand their business by targeting emerging and niche markets. Market share data is given on both global and regional levels. Regions covered in the report are North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. Research analysts assess the market positions of the leading competitors and provide competitive analysis for each company. For this study, this report segments the global Biobanking market on the basis of product, application, and region:

Segments Covered in this report are:

Product & Services Outlook (Revenue, USD Billion; 2018–2030)

Equipment

Storage Equipment

Sample Transport Equipment

Sample Processing Equipment

Sample Analysis Equipment

Consumables

Collection Consumables

Storage Consumables

Processing Consumables

Analysis Consumables

Services

Supply Services

Processing Services

Storage Services

Transport Services

Software

Sample Type Outlook (Revenue, USD Billion; 2018–2030)

Biological Fluids

Human Tissues

Blood Products

Nucleic Acids

Human Waste Products

Cell Lines

Storage Type Outlook (Revenue, USD Billion; 2018–2030)

Automated Storage

Manual Storage

Browse Full Report Description + Research Methodology + Table of Content + Infographics@ https://www.emergenresearch.com/industry-report/biobanking-market

Major Geographies Analyzed in the Report:

North America (U.S., Canada)

Europe (U.K., Italy, Germany, France, Rest of EU)

Asia Pacific (India, Japan, China, South Korea, Australia, Rest of APAC)

Latin America (Chile, Brazil, Argentina, Rest of Latin America)

Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)

ToC of the report:

Chapter 1: Market overview and scope

Chapter 2: Market outlook

Chapter 3: Impact analysis of COVID-19 pandemic

Chapter 4: Competitive Landscape

Chapter 5: Drivers, Constraints, Opportunities, Limitations

Chapter 6: Key manufacturers of the industry

Chapter 7: Regional analysis

Chapter 8: Market segmentation based on type applications

Chapter 9: Current and Future Trends

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Life Sciences BPO Market: Key Trends and Growth Drivers

The global life sciences BPO market size is expected to reach USD 827.5 billion by 2030, registering a CAGR of 9.3% over the forecast years, according to a new report by Grand View Research, Inc. The rising costs of drug development; pre-clinical and clinical trials; and post-marketing surveillance; a rise in the patent cliff; a growing product pipeline; and regulatory constraints are some of the major factors driving the market. The pharmaceutical and biotech industries invest heavily in the R&D sector to continuously introduce new molecules, devices, and treatments. The different stages of drug development, such as drug discovery, pre-clinical studies, and clinical trials, require huge financial, technological, and human resources.

To cater to the growing needs of the industry, the outsourcing vendors are expanding their product and service offerings and they are targeting niche areas for long-term growth and profitability. Altogether, these trends are expected to boost the life sciences outsourcing market over the forecast period. During the COVID-19 pandemic, a significant number of outsourcing providers expanded their existing manufacturing and research facilities to meet the growing demand for COVID-19 vaccines and diagnostics. Even post-pandemic, CDMOs are practicing similar strategies to support the future demand for pharmaceuticals. For instance, in April 2022, Aenova Group developed a new facility for manufacturing highly potent drugs with an investment of EUR 10 million.

The adoption of such strategies by the market players is expected to be profitable for the market. There has been a rising demand to reduce the cost of manufacturing and development of drugs and medical devices. Outsourcing manufacturing, research, and marketing services provide pharmaceutical and medical device companies with cost- and time-saving benefits. This is expected to have a positive impact on the market. Over the years, mergers and acquisition deals between CROs and CDMOs have increased. The rising demand for clinical services and the growing need for specialized service providers to improve the focus on their core competencies are some of the factors that are expected to drive the incidence of M&A deals.

Gather more insights about the market drivers, restrains and growth of the Life Sciences BPO Market

Life Sciences BPOMarket Report Highlights

• The increasing number of M&A transactions has broadened the global reach and improved the capabilities of CROs and CDMOs to provide end-to-end services; a continuation of this trend is expected to benefit the market significantly

• COVID-19 incidence has decreased significantly as a result of a growing global vaccination campaign

• Owing to this, the CRO and CDMO are now refocusing on developing drugs for oncology and other diseases owing to their high burden

• For instance, in April 2022, Labcorp collaborated with Xcell Biosciences to support the company in developing cell and gene therapies for treating cancer, Parkinson’s, and other rare diseases

• Such initiatives by the CDMOs are likely to profit the market owing to the high effectiveness of gene therapy in treating cancer and other rare diseases

• The medical device segment is expected to register the fastest CAGR from 2023 to 2030 due to the complexities associated with medical device designing

• The strict regulatory framework for medical device approval globally has further contributed to the demand for medical device outsourcing services

• Asia Pacific held the largest revenue share in 2022 due to the presence of a significant number of CROs providing cost-effective BPO services

Life Sciences BPO Market Segmentation

Grand View Research has segmented the global life sciences BPO market based on service and region:

Life Sciences BPO Services Outlook (Revenue, USD Billion, 2018 - 2030)

• Pharmaceutical outsourcing

o Contract Manufacturing Market

o API

o Finished Dose Form

o Packaging

o Contract Research Organizations

o Drug Discovery

o Pre-clinical Studies

o Clinical Trial Studies

o Regulatory Services

o Pharmacovigilance

• Medical Devices Outsourcing

o Contract Manufacturing Market

o Electronic Manufacturing Services

o Finished Goods

o Raw Materials/ Components

o Contract Research Organizations

o Regulatory Consulting Services

o Product Design and Development Services

o Product Testing Services

o Product Implementation Services

o Product Upgrade Services

o Product Maintenance Services

• Contract sales and marketing outsourcing

• Others

Life Sciences BPO Regional Outlook (Revenue, USD Billion, 2018 - 2030)

• North America

o U.S.

o Canada

• Europe

o UK

o Germany

o France

o Italy

o Spain

o Denmark

o Sweden

o Norway

• Asia Pacific

o Japan

o China

o India

o Australia

o Thailand

o South Korea

• Latin America

o Brazil

o Mexico

o Argentina

• Middle East and Africa

o South Africa

o Saudi Arabia

o UAE

o Kuwait

Order a free sample PDF of the Life Sciences BPO Market Intelligence Study, published by Grand View Research.

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The Future of Gene Synthesis: Market Analysis and Key Insights

The global gene synthesis market size is expected to reach USD 5.78 billion by 2030, registering a CAGR of 16.1% from 2023 to 2030 according to a new report by Grand View Research, Inc. Development of the market is due  to the growing investment in the synthetic biology field, favorable government regulations, and technological advancements in the gene synthesis market. In January 2022, synthetic DNA manufacturer Twist Bioscience announced plans of developing EDS technology at the J.P. Morgan Health Care Conference. The company established an enzymatic DNA synthesis technology that is novel, low-cost, scarless, and scalable.

The introduction of novel DNA synthesis platforms with technologically advanced specifications that address the increased demand of researchers is also contributing to the overall growth. For instance, in June 2021, DNA Script introduced the SYNTAX System, which is the nucleic acid printer based on EDS technology. Similarly, in December 2020, Evonetix Ltd. entered into a research collaboration with Analog Devices, Inc. Under the terms of the agreement, the companies collaborated on Evonetix's Microelectromechanical System-based silicon chips' improvement and commercial scale-up, as well as the development of a DNA desktop writer.

Researchers, as well as biotechnology and pharmaceutical corporations, have become increasingly interested in targeted therapy during recent years. It has become a popular method of disease management. In the near future, targeted therapy in conjunction with chemotherapy and immunotherapy is likely to develop significantly, presenting lucrative prospects for both emerging & established competitors in the gene synthesis market.

Key players are focusing on product development and are entering into partnerships and collaborations to expand their product offerings. For instance, In January 2022, Thermo Fisher Scientific, Inc. completed the acquisition of PeproTech, Inc.- a producer of antibodies and vectors. This acquisition may help the company strengthen its position in the market. Similarly, in July 2021, GenScript hosted the GenScript Gene & Cell Engineering Virtual Summit. This event focused on highlighting synthetic biology research to enhance protein design, drug discovery, and genome editing, enabling the company to increase its customer base.

Gene Synthesis Market Report Highlights

The growth is attributed to the growing demand for the synthetic biology, coupled with increasing government support to offer funds for R&D initiatives in synthetic biology

By method, solid-phase synthesis dominated in 2022 as it offers high accuracy and is a prominent technology for the applications in several fields and for various research purposes

By services, antibody DNA synthesis dominated the gene synthesis market in 2022, owing to the presence of significant players such as Synbio offers services, Twist Bioscience Corporation, and others, offering services in this segment

By application, the gene & cell therapy development segment dominated the gene synthesis market in 2022. This is attributed to the growing number of R&D programs for the development of cell and gene therapies

By end-use, academic and government research institute dominated the gene synthesis market in 2022, as most of the gene synthesis process is performed in the research settings for clinical research and investigational programs

North America captured the highest share in 2022 owing to the well-established molecular biology infrastructure along with the presence of a significant number of market players in the region

Gene Synthesis Market Segmentation

Grand View Research has segmented the global gene synthesis market report based on the method, services, application, end-use, and region:

Gene Synthesis Method Outlook (Revenue, USD Million, 2018 - 2030)

Solid-phase Synthesis

Chip-based Synthesis

PCR-based Enzyme Synthesis

Gene Synthesis Services Outlook (Revenue, USD Million, 2018 - 2030)

Antibody DNA Synthesis

Viral DNA Synthesis

Others

Gene Synthesis Application Outlook (Revenue, USD Million, 2018 - 2030)

Gene & Cell Therapy Development

Vaccine Development

Disease Diagnosis

Others

Gene Synthesis End-use Outlook (Revenue, USD Million, 2018 - 2030)

Biotechnology & Pharmaceutical Companies

Academic & Government Research Institutes

Contract Research Organizations

Gene Synthesis Regional Outlook (Revenue, USD Million, 2018 - 2030)

North America

US

Canada

Europe

Germany

UK

France

Italy

Spain

Denmark

Sweden

Norway

Asia Pacific

China

India

Japan

South Korea

Australia

Thailand

Latin America

Brazil

Mexico

Argentina

Middle East & Africa

South Africa

Saudi Arabia

UAE

Kuwait

Key Players

GenScript

Brooks Automation, Inc. (GENEWIZ)

Boster Biological Technology

Twist Bioscience

ProteoGenix, Inc

Biomatik

ProMab Biotechnologies, Inc.

Thermo Fisher Scientific, Inc.

Integrated DNA Technologies, Inc.

OriGene Technologies, Inc.

Order a free sample PDF of the Gene Synthesis Market Intelligence Study, published by Grand View Research.

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The Pharmaceutical CDMO Services Market is projected to grow from USD 146010 million in 2024 to an estimated USD 254648.4 million by 2032, with a compound annual growth rate (CAGR) of 7.2% from 2024 to 2032.The pharmaceutical Contract Development and Manufacturing Organization (CDMO) services market has witnessed significant growth in recent years, driven by the rising demand for cost-effective and efficient drug development processes. CDMOs have become pivotal in the pharmaceutical industry, providing comprehensive services that span from drug development to manufacturing. This article delves into the dynamics shaping this market, its key drivers, and the challenges it faces.CDMOs offer specialized services to pharmaceutical companies, including formulation development, clinical trial production, and large-scale commercial manufacturing. These organizations bridge the gap between innovative drug discovery and scalable manufacturing, enabling pharmaceutical companies to focus on their core competencies.

Browse the full report https://www.credenceresearch.com/report/pharmaceutical-cdmo-services-market

Market Drivers

Several factors are fueling the expansion of the pharmaceutical CDMO services market:

1. Outsourcing Trends: Increasingly, pharmaceutical companies are outsourcing their development and manufacturing processes to CDMOs to reduce costs, improve efficiency, and access specialized expertise. This trend is especially prominent among small and medium-sized pharmaceutical firms that lack in-house capabilities.

2. Rising Drug Demand:

The global rise in chronic diseases such as diabetes, cardiovascular disorders, and cancer has led to a surge in drug demand. This has compelled pharmaceutical companies to scale up production rapidly, creating opportunities for CDMOs.

3. Biologics and Biosimilars Growth: The rapid development of biologics and biosimilars has created a need for advanced manufacturing technologies and facilities, which many CDMOs possess. This has positioned them as indispensable partners for biopharmaceutical companies.

4. Regulatory Complexity: The stringent regulatory environment in the pharmaceutical industry necessitates compliance with international standards. CDMOs often have the necessary certifications and expertise to navigate these challenges, making them attractive collaborators.

5. Technological Advancements: Innovations in drug delivery systems, such as nanoparticle-based therapies and cell and gene therapies, have increased the complexity of drug manufacturing. CDMOs have invested heavily in adopting cutting-edge technologies, enabling them to meet these demands effectively.

Key Segments in the CDMO Market

1. Drug Development: This segment involves preclinical and clinical development services, including formulation and analytical services. The increasing number of clinical trials globally has propelled the demand for development services.

2. Manufacturing: CDMOs provide manufacturing solutions for active pharmaceutical ingredients (APIs) and finished dosage forms. The growing need for high-volume production of generic drugs and novel formulations has boosted this segment.

3. Packaging and Logistics: With the rise of biologics and temperature-sensitive drugs, the demand for specialized packaging and logistics services has grown, further expanding the CDMO market.

Challenges in the CDMO Market

Despite its growth, the CDMO market faces challenges, including:

- Regulatory Hurdles: Compliance with diverse global regulatory standards can be complex and costly.

- Capacity Constraints: The rapid growth in demand often exceeds the production capacity of many CDMOs, leading to delays.

- Intellectual Property Concerns: Pharmaceutical companies may be hesitant to outsource critical stages of drug development due to fears of intellectual property theft or leakage.

Future Outlook

The pharmaceutical CDMO services market is poised for robust growth, driven by advancements in technology, increasing drug development activities, and the growing complexity of pharmaceutical manufacturing. The focus on biologics, biosimilars, and personalized medicine will further enhance the demand for specialized CDMO services.

Key Player Analysis:

Bushu Pharmaceuticals Ltd.

Cambrex Corporation

Catalent, Inc

Cordenpharma International

Laboratory Corporation of America Holdings

Lonza Group AG

Nipro Corporation

Piramal Pharma Solutions

Recipharm Ab

Samsung Biologics

Siegfried Holding Ag

Thermo Fisher Scientific Inc.

Wuxi Apptec

Segmentation:

By Product 

API

Type

Traditional Active Pharmaceutical Ingredient (Traditional API)

Highly Potent Active Pharmaceutical Ingredient (HP-API)

Antibody Drug Conjugate (ADC)

Others

Synthesis

Synthetic

Solid

Liquid

Biotech

Drug

Innovative

Generics

Manufacturing

Continuous manufacturing

Batch manufacturing

Drug Product

Oral solid dose

Semi-solid dose

Liquid dose

Others

By Workflow 

Clinical

Commercial

By Application 

Oncology

Small Molecules

Biologics

Infectious Diseases

Neurological Disorders

Cardiovascular Disease

Metabolic Disorders

Autoimmune Diseases

Respiratory Diseases

Ophthalmology

Gastrointestinal Disorders

Hormonal Disorders

Hematological Disorders

Others

By End-use 

Small Pharmaceutical Companies

Medium Pharmaceutical Companies

Large Pharmaceutical Companies

By Regional

North America

U.S.

Canada

Mexico

Europe

Germany

France

U.K.

Italy

Spain

Rest of Europe

Asia Pacific

China

Japan

India

South Korea

South-east Asia

Rest of Asia Pacific

Latin America

Brazil

Argentina

Rest of Latin America

Middle East & Africa

GCC Countries

South Africa

Rest of the Middle East and Africa

Browse the full report https://www.credenceresearch.com/report/pharmaceutical-cdmo-services-market

Contact:

Credence Research

Please contact us at +91 6232 49 3207

Email: sales@credenceresearch.com

Website: www.credenceresearch.com

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Meticulous Research® Projects Global Pharmaceutical Contract Development & Manufacturing Market to Reach $261.57 Billion by 2031

Meticulous Research®, a leading global market intelligence and consulting firm, has released its latest report titled Pharmaceutical Contract Development & Manufacturing Market Size, Share, Forecast, & Trends Analysis by Service and End User – Global Forecast to 2031. According to the report, the pharmaceutical contract development and manufacturing market is poised to reach an impressive $261.57 billion by 2031, registering a compound annual growth rate (CAGR) of 7.4% from 2024 to 2031.

Download Complete Sample PDF Copy Here: https://www.meticulousresearch.com/download-sample-report/cp_id=5171

Key Market Drivers and Challenges

The expanding pharmaceutical contract development and manufacturing market is being driven by several critical factors. The increasing complexity of pharmaceutical manufacturing processes, coupled with manufacturers' adoption of advanced technologies, is fueling growth. In addition, growing investments in pharmaceutical research and development (R&D), the expiration of patents, and heightened demand for generic medicines and biologics are expected to further propel the market.

However, several challenges, including disruptions in the supply chain and stringent government regulations, are hindering growth. The market also faces ongoing issues related to intellectual property risks and a shortage of skilled professionals, posing significant challenges to sustained expansion.

Emerging Opportunities

Despite these hurdles, the pharmaceutical contract development and manufacturing market is expected to witness robust opportunities, particularly in the fields of cell and gene therapies, personalized medicine, and high-potency active pharmaceutical ingredients (HPAPI). The growing demand for antibody-drug conjugates (ADCs) is also projected to open new avenues for market participants.

Quick Buy: https://www.meticulousresearch.com/Checkout/67156803

Competitive Landscape

Key players in the global pharmaceutical contract development and manufacturing market include industry giants such as Lonza Group Ltd. (Switzerland), Catalent Inc. (U.S.), Patheon (a subsidiary of Thermo Fisher Scientific Inc., U.S.), Recipharm AB (Sweden), and WuXi Biologics Inc. (China), among others. These companies continue to play a vital role in shaping the market through strategic collaborations, technological advancements, and capacity expansions.

Future Outlook by Service Type and End User

The market is segmented into key service categories, including pharmaceutical manufacturing (API and FDF), drug development, and biologics manufacturing. Of these, the biologics manufacturing services segment is projected to grow at the fastest rate, with an estimated CAGR of 11.1% during the forecast period. Within this segment, Finished Dosage Forms (FDF) manufacturing services, driven by the complexity of biologics manufacturing, are expected to witness particularly high demand.

Check complete table of contents with list of table and figures: https://www.meticulousresearch.com/product/pharmaceutical-contract-development-and-manufacturing-market-5171

On the basis of end users, large pharmaceutical companies are anticipated to dominate the market, accounting for 42.3% of the global share in 2024. The reliance of major pharmaceutical and biotech companies on external contract manufacturers, driven by increasing R&D complexity and the rising costs of maintaining in-house facilities, is a major factor contributing to this trend.

Geographic Insights

Regionally, North America is projected to capture the largest share of the market, accounting for 44.3% in 2024. The region's dominance is attributed to a combination of factors, including a diversified pharmaceutical pipeline, increased demand for biologics and generic drugs, and a robust base for clinical trials and API production. The presence of leading pharmaceutical companies and advanced manufacturing capabilities further bolster North America's market position.

Request  Sample PDF Copy Here: To gain deeper insights into the pharmaceutical contract development and manufacturing market, including growth opportunities, competitive analysis, and geographical trends, download the sample report here: https://www.meticulousresearch.com/request-sample-report/cp_id=5171

Key Questions Addressed in the Report:

What are the fastest-growing market segments by type, end user, and region?

What was the historical market size, and what are the forecasts through 2031?

What are the key market drivers, challenges, and emerging opportunities?

Who are the leading players, and what strategies are they employing?

Which regions are expected to witness the highest growth?

Contact Information:

Meticulous Research® Email: sales@meticulousresearch.com Sales Contact: +1-646-781-8004 Connect with us on LinkedIn

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Vector Purification Market To Surge At 21% CAGR Aided By Rising Cancer Research Activities

The Vector Purification Market is driven by the increasing prevalence of cancer and the need for therapeutic vectors in gene therapy and vaccine development. The vector purification process helps in isolating the recombinant virus or non-viral vectors from host cell lysates or media and removes any contaminating host cell components. This purification is crucial for ensuring the safety and efficacy of engineered vectors in therapeutics and vaccine applications. Vectors are essential tools used for introducing new genetic material into cells. Common vectors include viruses and non-viral systems such as plasmids, which can be engineered to carry therapeutic genes into targeted host cells. Purification removes any contaminating toxic cellular components or proteins, live or dead host cells, media components, and impurities from the final vector preparation.

The Vector Purification Market is estimated to be valued at US$ 336 Mn in 2024 and is expected to exhibit a CAGR of 21% over the forecast period 2024-2031.

Key Takeaways

Key players operating in the vector purification market are Agilent Technologies, BIA Separations, Bio-Rad Laboratories, Merck, and Thermo Fisher Scientific.

Growing incidence of cancer and genetic disorders is fueling the demand for gene and cell therapies with engineered vectors. This is driving significant research investments into developing advanced vector systems, propelling the need for large-scale vector purification.

Technological advancements include automated large-scale purification systems using affinity chromatography, size-exclusion chromatography, and other methods optimized for clinical-grade vectors. Companies are also developing specialized resins and kits tailored for specific vector platforms to streamline purification workflows.

Market Trends

Growing adoption of adeno-associated viral vectors - AAV vectors have emerged as the preferred gene delivery tool due to their low pathogenicity and ability to transduce non-dividing cells. This is spurring increased R&D utilizing AAV systems.

Continuous processing technologies - Continuous multi-column purification systems coupled with in-line monitoring are being introduced to enhance process scalability and vector yields for clinical and commercial applications.

Market Opportunities

Developing economies in Asia Pacific and Latin America present lucrative opportunities for vector purification product suppliers and contract service providers, driven by increased government funding for cell and gene therapy research.

Custom purification solutions - Partnering with clinical developers to provide tailored resins, chromatography methods and single-use kits optimized for specific vectors could capture a larger share of the high-growth advanced therapy market.

Impact of COVID-19 on Vector Purification Market Growth

The COVID-19 pandemic has significantly impacted the growth of the vector purification market. With lockdowns imposed across various regions, research activities slowed down drastically impacting the demand for vector purification kits, columns and other products. Social distancing measures also disrupted the supply chain to some extent. However, with the pandemic accelerating research on vaccine and therapeutics development, the need for DNA and RNA purification increased rapidly. Several biopharma companies accelerated their clinical trials and manufacturing operations focusing on COVID-19 treatment and prevention.

Post pandemic, the vector purification market is expected to witness robust growth. With rising investments to boost preparedness for future pandemics, research focusing on vaccine development and gene therapy is likely to increase. Several contract manufacturing and custom services companies have also expanded their capabilities to support clinical trials and commercial manufacturing of cell and gene therapies. This would drive the demand for high quality and reproducible purification solutions. Additionally, continued expansion of regenerative medicine applications and advancement of gene editing tools would further propel the market growth. Key players are actively investing in portfolio expansion and automation technology to increase throughput and reproducibility.

Europe contributed the largest revenue share to the Vector Purification Market owing to significant research focus and presence of major market players. However, Asia Pacific represented the fastest growing regional market and is anticipated to overtake Europe during the forecast period. This can be attributed to rising healthcare investments, increasing biotech research workforce and strengthening manufacturing capabilities in major Asian countries including China, India and South Korea. The growing geriatric population base and rising incidence of genetic disorders also present lucrative opportunities.

As countries seek to reduce dependence on imported vaccines and biologics, focus is growing on boosting domestic manufacturing capabilities. This presents immense opportunities for vector purification solution providers to assist various regional and contract manufacturing organizations with technology transfer and process development projects. Key strategies for market players should include partnerships with regional clinical research organizations, establishment of local technical centres and development of affordable product offerings.

Get more insights on this topic:  https://www.trendingwebwire.com/vector-purification-market-is-estimated-to-witness-high-growth-owing-to-automation-technologies/

Author Bio:

Alice Mutum is a seasoned senior content editor at Coherent Market Insights, leveraging extensive expertise gained from her previous role as a content writer. With seven years in content development, Alice masterfully employs SEO best practices and cutting-edge digital marketing strategies to craft high-ranking, impactful content. As an editor, she meticulously ensures flawless grammar and punctuation, precise data accuracy, and perfect alignment with audience needs in every research report. Alice's dedication to excellence and her strategic approach to content make her an invaluable asset in the world of market insights. (LinkedIn: www.linkedin.com/in/alice-mutum-3b247b137 )

What Are The Key Data Covered In This Vector Purification Market Report?

:- Market CAGR throughout the predicted period

:- Comprehensive information on the aspects that will drive the Vector Purification Market's growth between 2024 and 2031.

:- Accurate calculation of the size of the Vector Purification Market and its contribution to the market, with emphasis on the parent market

:- Realistic forecasts of future trends and changes in consumer behaviour

:- Vector Purification Market Industry Growth in North America, APAC, Europe, South America, the Middle East, and Africa

:- A complete examination of the market's competitive landscape, as well as extensive information on vendors

:- Detailed examination of the factors that will impede the expansion of Vector Purification Market vendors

FAQ’s

Q.1 What are the main factors influencing the Vector Purification Market?

Q.2 Which companies are the major sources in this industry?

Q.3 What are the market’s opportunities, risks, and general structure?

Q.4 Which of the top Vector Purification Market companies compare in terms of sales, revenue, and prices?

Q.5 Which businesses serve as the Vector Purification Market’s distributors, traders, and dealers?

Q.6 How are market types and applications and deals, revenue, and value explored?

Q.7 What does a business area’s assessment of agreements, income, and value implicate?

*Note: 1. Source: Coherent Market Insights, Public sources, Desk research 2. We have leveraged AI tools to mine information and compile it

[skyquesttinsights]

Cell Therapy Industry: Trends and Market Insights 2024-2031

In recent years, cell therapy has emerged as a revolutionary approach in the realm of medical treatments, offering promising solutions for various chronic and life-threatening conditions. This innovative field harnesses the potential of living cells to treat diseases by repairing or replacing damaged tissues and organs. The cell therapy market is experiencing significant growth, driven by advancements in technology, increased research and development activities, and a rising prevalence of chronic diseases.

According to recent industry reports, the global cell therapy market is on a robust growth trajectory. Global Cell Therapy Market size was valued at USD 3.9 Billion in 2022 and is poised to grow from USD 6.7 Billion in 2023 to USD 190.91 Billion by 2031, growing at a CAGR of 52% during the forecast period (2024-2031). This growth is attributed to several factors, including technological advancements, a surge in clinical trials, and the increasing demand for personalized medicine.

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Key Market Drivers

1. Technological Advancements: Breakthroughs in cell processing technologies, gene editing techniques such as CRISPR, and improvements in manufacturing processes are driving the market. These advancements enhance the efficacy and safety of cell therapies, making them more accessible and effective for patients.

2. Rising Prevalence of Chronic Diseases: The growing incidence of chronic conditions such as cancer, cardiovascular diseases, and autoimmune disorders is fueling the demand for cell-based treatments. Cell therapy offers potential cures and long-term solutions for these persistent health challenges.

3. Increased Research and Development: Ongoing research efforts and clinical trials are expanding the applications of cell therapy. Investment in R&D by pharmaceutical companies and biotech firms is crucial for discovering new therapies and improving existing ones.

4. Regulatory Support: Regulatory agencies are increasingly providing clearer pathways for the approval and commercialization of cell therapies. This supportive regulatory environment is crucial for accelerating the development and market entry of new treatments.

Market Segmentation

The cell therapy market is segmented based on cell type, application, and geography.

- By Cell Type: The market includes various types of cells such as stem cells, T-cells, and dendritic cells. Stem cell therapies are particularly prominent due to their potential in regenerative medicine.

- By Application: Applications span across oncology, cardiovascular diseases, neurological disorders, and more. Oncology holds a significant share, driven by the development of CAR-T cell therapies.

- By Geography: North America dominates the market, followed by Europe and the Asia-Pacific region. The strong presence of key players and advanced healthcare infrastructure contribute to North America's leading position.

To establish the important thing traits, Ask Our Experts @ https://www.skyquestt.com/speak-with-analyst/cell-therapy-market

Cell Therapy Market Top Players' Company Profiles - Thermo Fisher Scientific, Inc., Merck KGaA, Danaher Corporation, Becton, Dickinson, and Company, Lonza Group, Sartorius AG, Nkarta, Inc., Aurion Biotech, S. BIOMEDICS, MEDIPOST, Anterogen Co., Ltd., JW Therapeutics, JCR Pharmaceuticals Co., Ltd., Johnson & Johnson Services, Inc, Bristol-Myers Squibb Company, Gilead Sciences, Inc., Novartis AG, Intellia Therapeutics, Iovance Therapeutics, CRISPR Therapeutics

Challenges and Opportunities

Despite its promising prospects, the cell therapy market faces several challenges, including high treatment costs, complex manufacturing processes, and regulatory hurdles. However, these challenges also present opportunities for innovation and improvement. Advances in manufacturing technologies, cost reduction strategies, and streamlined regulatory processes could further propel the growth of the market. The cell therapy market is poised for significant growth, driven by technological advancements, rising disease prevalence, and supportive regulatory environments. As the field continues to evolve, it holds the potential to transform the landscape of medical treatments and improve patient outcomes worldwide. Stakeholders in the healthcare industry must stay abreast of these developments to capitalize on the opportunities presented by this dynamic market.

[mitalipingale]

The Cell and Gene Therapy Manufacturing Services Market in 2023 is US$ 6 billion, and is expected to reach US$ 22.14 billion by 2031 at a CAGR of 17.70%.

[global-research-report]

Elevate Your Biopharma Pipeline with Reliable Plasmid DNA Manufacturing

The global plasmid DNA manufacturing market size is expected to reach USD 6.70 billion by 2030, expanding at a CAGR of 21.44% from 2025 to 2030, according to a new report by Grand View Research, Inc. The rising prevalence of chronic diseases, combined with the wide application scope of plasmid DNA in the healthcare industry is expected to drive the industry growth. Plasmid DNA can be used directly for therapeutic applications, such as the production of vaccine antigens or gene therapy. Moreover, it can be utilized for various research purposes, such as gene cloning, gene mapping, etc. The rising number of patients choosing gene therapy is expected to drive industry growth in the coming years.

According to clinicaltrials.gov, the number of cell & gene therapies across global pipeline programs (Phase I to Phase III trials) increased from 289 in 2018 to 327 in 2022. Furthermore, the U.S. FDA provides constant support for innovations in the advanced therapy arena via several policies concerning product manufacturing. With increased cell and gene therapy products, the industry will see an increased need for manufacturing plasmid DNA on a larger scale. The COVID-19 pandemic is anticipated to positively impact industry growth. For instance, in September 2021, India approved the first COVID-19 DNA vaccine. It is the world’s first COVID-19 DNA vaccine manufactured in partnership with DBT-BIRAC as part of Mission COVID Suraksha.

Circular DNA is used in India’s ZyCoV-D vaccination to protect against COVID-19 infection. Furthermore, key entities in the global industry are undertaking various strategic initiatives to strengthen their market presence, which is also expected to propel growth. For instance, in June 2022, BioCina announced the expansion of the production of plasmid DNA in a new dedicated GMP suite to its offering of CDMO services. The suite has a single-use fermentation capacity of up to 300 L and appropriately scaled downstream processing machinery.

Plasmid DNA Manufacturing Market Report Highlights

MP-grade plasmid DNA manufacturing dominated the market in 2024 with a share of 86.29% and is expected to grow at the fastest CAGR over the forecast period.

The clinical therapeutics segment held the largest market share of 54.6% in 2024. Plasmid DNA is currently increasing in importance for clinical research applications in genetic vaccination and gene therapy.

The cell & gene therapy segment held the largest market share of 54.4% in 2024. This high share can be attributed to the fact that gene therapy is broadly applied in the treatment of several inherited and genetic diseases.

The cancer segment held the largest market share of 40.0% in 2024 and is expected to witness the fastest CAGR from 2025 to 2030.

The North America Plasmid DNA manufacturing market held the largest revenue share of 43.43% of the global market in 2024.

Plasmid DNA Manufacturing Market Segmentation

Grand View Research has segmented the global plasmid DNA manufacturing market on the basis of service, application, end use, and country:

Plasmid DNA Manufacturing Grade Outlook (Revenue, USD Million, 2018 - 2030)

R&D Grade

Viral Vector Development

AAV

Lentivirus

Adenovirus

Retrovirus

Others

mRNA Development

Antibody Development

DNA Vaccine Development

Others

GMP Grade

Plasmid DNA Manufacturing Development Phase Outlook (Revenue, USD Million, 2018 - 2030)

Pre-Clinical Therapeutics

Clinical Therapeutics

Marketed Therapeutics 

Plasmid DNA Manufacturing Application Outlook (Revenue, USD Million, 2018 - 2030)

DNA Vaccines

Cell & Gene Therapy

Immunotherapy

Others

Plasmid DNA Manufacturing Disease Outlook (Revenue, USD Million, 2018 - 2030)

Infectious Disease

Cancer

Genetic Disorder

Others

Plasmid DNA Manufacturing Regional Outlook (Revenue, USD Million, 2018 - 2030)

North America

US

Canada

Mexico

Europe

Germany

UK

France

Italy

Spain

Denmark

Sweden

Norway

Asia Pacific

China

Japan

India

South Korea

Australia

Thailand

Latin America

Brazil

Argentina

Middle East & Africa

South Africa

Saudi Arabia

UAE

Kuwait

List of Key Players

Charles River Laboratories

VGXI, Inc.

Danaher (Aldevron)

Kaneka Corp.

Nature Technology

Cell and Gene Therapy Catapult

Eurofins Genomics

Lonza

Luminous BioSciences, LLC

Akron Biotech

Order a free sample PDF of the Plasmid DNA Manufacturing Market Intelligence Study, published by Grand View Research.

[spookysaladchaos]

Global Top 5 Companies Accounted for 85% of total Hearing Loss Therapy market (QYResearch, 2021)

Hearing loss therapy refers to the latest technological advances and treatment options for people with hearing impairment, including Ear-Based Hearing Aids, bone anchors, cochlear implants and mixed arteries, auditory brainstem implants, and the transfer of genes to the inner ear through stem cell therapy and hair cell regeneration for the treatment of sensorineural hearing loss.

In this report, we mainly study the medical devices for hearing loss therapy.

According to the new market research report “Global Hearing Loss Therapy Market Report 2023-2029”, published by QYResearch, the global Hearing Loss Therapy market size is projected to reach USD 16.2 billion by 2029, at a CAGR of 7.0% during the forecast period.

Figure.   Global Hearing Loss Therapy Market Size (US$ Million), 2018-2029

Figure.   Global Hearing Loss Therapy Top 14 Players Ranking and Market Share（Based on data of 2021, Continually updated）

The global key manufacturers of Hearing Loss Therapy include Sonova, William Demant, WS Audiology, Cochlear, GN ReSound, Starkey, MED-EL, Rion, Audina Hearing Instruments, Sebotek Hearing Systems, etc. In 2021, the global top five players had a share approximately 85.0% in terms of revenue.

About QYResearch

QYResearch founded in California, USA in 2007.It is a leading global market research and consulting company. With over 16 years’ experience and professional research team in various cities over the world QY Research focuses on management consulting, database and seminar services, IPO consulting, industry chain research and customized research to help our clients in providing non-linear revenue model and make them successful. We are globally recognized for our expansive portfolio of services, good corporate citizenship, and our strong commitment to sustainability. Up to now, we have cooperated with more than 60,000 clients across five continents. Let’s work closely with you and build a bold and better future.

QYResearch is a world-renowned large-scale consulting company. The industry covers various high-tech industry chain market segments, spanning the semiconductor industry chain (semiconductor equipment and parts, semiconductor materials, ICs, Foundry, packaging and testing, discrete devices, sensors, optoelectronic devices), photovoltaic industry chain (equipment, cells, modules, auxiliary material brackets, inverters, power station terminals), new energy automobile industry chain (batteries and materials, auto parts, batteries, motors, electronic control, automotive semiconductors, etc.), communication industry chain (communication system equipment, terminal equipment, electronic components, RF front-end, optical modules, 4G/5G/6G, broadband, IoT, digital economy, AI), advanced materials industry Chain (metal materials, polymer materials, ceramic materials, nano materials, etc.), machinery manufacturing industry chain (CNC machine tools, construction machinery, electrical machinery, 3C automation, industrial robots, lasers, industrial control, drones), food, beverages and pharmaceuticals, medical equipment, agriculture, etc.

For more information, please contact the following e-mail address:

Email: global@qyresearch.com

Website: https://www.qyresearch.com

[lanettcdmo]

Dynamic Landscape of Pharmaceuticals: Key Trends and the Role of Contract Manufacturing

Introduction: In the dynamic realm of pharmaceuticals, staying abreast of key trends is essential for industry players seeking to innovate and adapt. From precision medicine to digital health, the landscape is constantly evolving, presenting both challenges and opportunities. In this blog post, we’ll explore the pivotal role of contract manufacturing and regulatory support amidst these trends, shedding light on their significance in driving progress and ensuring compliance in the pharmaceutical industry.

Precision Medicine and Contract Manufacturing:

Precision medicine, with its focus on personalized therapies, presents unique manufacturing challenges due to the need for small batch sizes and customized formulations. Contract manufacturing organizations (CMOs) are playing a vital role in this space by offering flexible manufacturing solutions tailored to the specific needs of precision medicine products.

CMOs specializing in advanced manufacturing technologies, such as continuous manufacturing and 3D printing, are enabling pharmaceutical companies to accelerate the development and production of personalized therapies, enhancing efficiency and scalability.

Digital Health and Regulatory Support:

The integration of digital health solutions into pharmaceutical products necessitates robust regulatory support to ensure compliance with evolving standards and guidelines. Regulatory consulting firms provide invaluable expertise in navigating the complex regulatory landscape, helping companies secure approvals for digital therapeutics, mobile health apps, and virtual clinical trials.

Regulatory support extends beyond product approvals to encompass post-market surveillance, pharmacovigilance, and compliance with data privacy regulations. By partnering with regulatory experts, pharmaceutical companies can mitigate risks, expedite market entry, and maintain compliance throughout the product lifecycle.

Biopharmaceuticals and Contract Manufacturing:

The growing demand for biopharmaceuticals, driven by their potential to address unmet medical needs, is driving expansion in the contract manufacturing market. CMOs with expertise in bioprocessing and cell culture technologies are in high demand, offering end-to-end manufacturing services for biologics, biosimilars, and cell and gene therapies.

Strategic partnerships between pharmaceutical companies and CMOs enable access to specialized capabilities and capacity, allowing for faster development and commercialization of biopharmaceutical products while mitigating capital investment risks.

Sustainability and Regulatory Compliance:

Sustainability considerations are increasingly influencing regulatory requirements in the pharmaceutical industry, with agencies emphasizing environmental stewardship and responsible manufacturing practices. Regulatory support firms assist companies in navigating sustainability regulations, ensuring compliance with environmental, health, and safety standards.

From green chemistry principles to waste reduction strategies, pharmaceutical companies are embracing sustainable manufacturing practices with the guidance of regulatory experts, aligning with global sustainability goals and enhancing their corporate social responsibility initiatives.

Conclusion:

As the pharmaceutical industry continues to evolve, the roles of contract manufacturing and regulatory support are becoming increasingly indispensable. From facilitating the production of precision medicines to navigating complex regulatory frameworks, these partners enable pharmaceutical companies to innovate responsibly and bring life-saving therapies to market efficiently. By leveraging the expertise of contract manufacturers and regulatory consultants, pharmaceutical companies can navigate the ever-changing landscape with confidence, driving progress and ensuring compliance in an era of unprecedented transformation.

[ashwetu]

Meticulous Research® Projects Global Pharmaceutical Contract Development & Manufacturing Market to Reach $261.57 Billion by 2031

Meticulous Research®, a leading global market intelligence and consulting firm, has released its latest report titled Pharmaceutical Contract Development & Manufacturing Market Size, Share, Forecast, & Trends Analysis by Service and End User – Global Forecast to 2031. According to the report, the pharmaceutical contract development and manufacturing market is poised to reach an impressive $261.57 billion by 2031, registering a compound annual growth rate (CAGR) of 7.4% from 2024 to 2031.

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Key Market Drivers and Challenges

The expanding pharmaceutical contract development and manufacturing market is being driven by several critical factors. The increasing complexity of pharmaceutical manufacturing processes, coupled with manufacturers' adoption of advanced technologies, is fueling growth. In addition, growing investments in pharmaceutical research and development (R&D), the expiration of patents, and heightened demand for generic medicines and biologics are expected to further propel the market.

However, several challenges, including disruptions in the supply chain and stringent government regulations, are hindering growth. The market also faces ongoing issues related to intellectual property risks and a shortage of skilled professionals, posing significant challenges to sustained expansion.

Emerging Opportunities

Despite these hurdles, the pharmaceutical contract development and manufacturing market is expected to witness robust opportunities, particularly in the fields of cell and gene therapies, personalized medicine, and high-potency active pharmaceutical ingredients (HPAPI). The growing demand for antibody-drug conjugates (ADCs) is also projected to open new avenues for market participants.

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Competitive Landscape

Key players in the global pharmaceutical contract development and manufacturing market include industry giants such as Lonza Group Ltd. (Switzerland), Catalent Inc. (U.S.), Patheon (a subsidiary of Thermo Fisher Scientific Inc., U.S.), Recipharm AB (Sweden), and WuXi Biologics Inc. (China), among others. These companies continue to play a vital role in shaping the market through strategic collaborations, technological advancements, and capacity expansions.

Future Outlook by Service Type and End User

The market is segmented into key service categories, including pharmaceutical manufacturing (API and FDF), drug development, and biologics manufacturing. Of these, the biologics manufacturing services segment is projected to grow at the fastest rate, with an estimated CAGR of 11.1% during the forecast period. Within this segment, Finished Dosage Forms (FDF) manufacturing services, driven by the complexity of biologics manufacturing, are expected to witness particularly high demand.

Check complete table of contents with list of table and figures: https://www.meticulousresearch.com/product/pharmaceutical-contract-development-and-manufacturing-market-5171

On the basis of end users, large pharmaceutical companies are anticipated to dominate the market, accounting for 42.3% of the global share in 2024. The reliance of major pharmaceutical and biotech companies on external contract manufacturers, driven by increasing R&D complexity and the rising costs of maintaining in-house facilities, is a major factor contributing to this trend.

Geographic Insights

Regionally, North America is projected to capture the largest share of the market, accounting for 44.3% in 2024. The region's dominance is attributed to a combination of factors, including a diversified pharmaceutical pipeline, increased demand for biologics and generic drugs, and a robust base for clinical trials and API production. The presence of leading pharmaceutical companies and advanced manufacturing capabilities further bolster North America's market position.

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Key Questions Addressed in the Report:

What are the fastest-growing market segments by type, end user, and region?

What was the historical market size, and what are the forecasts through 2031?

What are the key market drivers, challenges, and emerging opportunities?

Who are the leading players, and what strategies are they employing?

Which regions are expected to witness the highest growth?

Contact Information:

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