시장보고서
상품코드
2024974

바이러스 벡터 제조 시장 규모, 점유율, 동향 및 예측 : 유형, 질환, 용도, 최종사용자, 지역별(2026-2034년)

Viral Vector Manufacturing Market Size, Share, Trends and Forecast by Type, Disease, Application, End User, and Region, 2026-2034

발행일: | 리서치사: 구분자 IMARC | 페이지 정보: 영문 148 Pages | 배송안내 : 2-3일 (영업일 기준)

    
    
    




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※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

2025년의 세계 바이러스 벡터 제조 시장 규모는 17억 8,630만 달러로 평가되었습니다. 향후에 대해 IMARC Group은 2034년까지 시장 규모가 95억 4,990만 달러에 달하며, 2026-2034년에 CAGR 19.86%를 보일 것으로 예측하고 있습니다. 현재 북미가 시장을 독점하고 있으며, 2025년에는 49.3% 이상의 시장 점유율을 차지하고 있습니다. 유전성 질환의 유병률 증가, 유전자 치료의 보급 확대, 첨단 생명공학 인프라, 임상 시험 확대, 정부의 강력한 자금 지원, 탄탄한 R&D 투자, 그리고 주요 기업의 존재가 북미 바이러스 벡터 제조 시장을 주도하고 있습니다.

전 세계 바이러스 벡터 제조 시장은 유전성 질환 및 감염성 질환의 유병률 증가와 유전자 치료 및 세포 치료의 발전에 힘입어 괄목할 만한 성장세를 보이고 있습니다. 희귀질환, 암, 신경질환에 대한 혁신적인 치료법 개발에서 바이러스 벡터의 채택이 확대되고 있는 것이 수요를 증가시키는 주요 요인으로 작용하고 있습니다. 유전자 치료 임상 시험의 확대와 생명공학 및 제약 연구에 대한 정부의 투자 증가는 시장 확대를 더욱 촉진하고 있습니다. 또한 확장 가능한 제조 기술 개발과 생산 공정의 개선으로 바이러스 벡터 생산의 효율성과 비용 효율성이 향상되었습니다. 제약사 및 연구기관과의 협력 강화도 신규 치료제 개발을 가속화하고 있으며, 바이러스 벡터 제조 시장의 성장을 더욱 촉진하고 있습니다.

미국은 몇 가지 주요 요인에 힘입어 전체 시장 점유율의 91.90%를 차지하는 주요 시장 중 하나로 부상하고 있습니다. 중요한 촉진요인 중 하나는 유전성 질환과 암의 유병률 증가이며, 이로 인해 바이러스 벡터를 이용한 유전자 치료와 세포치료에 대한 수요가 증가하고 있습니다. 이러한 성장은 바이오테크놀러지에 대한 정부의 막대한 투자와 국내의 수많은 위탁개발생산기관(CDMO)의 존재가 지원하고 있습니다. 또한 확장 가능한 제조 기술의 발전으로 생산 효율성이 향상되어 치료용 바이러스 벡터에 대한 수요 증가에 대응하고 있습니다. 유전자치료제 파이프라인의 확대와 임상시험의 증가도 시장 확대에 기여하고 있으며, 미국은 바이러스 벡터 제조의 주요 거점으로서 입지를 다지고 있습니다.

바이러스 벡터 제조 시장 동향:

시장 성장과 투자

2024년 3월 18일 현재, FDA는 36건의 유전자 치료제를 승인했습니다. 개발중인 것은 500여 건에 달합니다. 식약처는 2025년까지 유전자치료제 분야에서 연간 10-20개의 제품을 승인할 것으로 예상하고 있습니다. 이러한 증가는 생명공학에 대한 투자 확대와 유전자 치료 분야에서 개발되고 있는 새로운 기술에 의해 촉진되고 있습니다. FDA의 적극적인 유전자치료제 규제 노력으로 일부 유전자치료제는 신속심사 대상에 포함돼 조기에 승인되었습니다. 연간 예상 승인 건수는 유전자 치료의 안전성 및 유효성 프로파일에 대한 신뢰가 높아지고 있음을 보여줍니다. 실제 승인된 유전자 치료제의 수와 풍부한 파이프라인은 큰 폭의 성장이 예상되는 활발한 시장을 말해주고 있습니다. 이러한 추세는 앞으로도 지속될 것으로 예상되며, 시장 확대는 혁신적인 치료법에 대한 FDA의 노력에 의해 크게 견인될 것입니다. 이러한 수요 증가에 대응하기 위해 제약사들은 유전자 치료제 수요 확대에 대응하기 위해 바이러스 벡터 생산에 많은 투자를 하고 있습니다. 이는 유전자 치료의 성공을 보장하기 위해서는 고품질 바이러스 벡터의 지속적인 공급이 필수적이기 때문입니다. 생산 규모 확대라는 과제를 극복하기 위해서는 FDA의 지원과 제조 인프라에 대한 업계의 투자가 필수적입니다. 이러한 노력은 더 많은 환자들이 유전자 치료의 혜택을 받을 수 있도록 하는 것을 목표로 하고 있습니다.

기술 발전과 프로세스 최적화

시장 성장은 세포주 개발 및 제조 공정 개선과 같은 바이러스 벡터 생산의 기술적 진보에 의해 주도되고 있습니다. 안정적인 포장용 세포주는 바이러스 벡터의 생산 효율을 높여 시장 성장을 촉진하고 있습니다. 예를 들어 삼성바이오로직스가 채택한 HEK293 세포주 기술은 2022년 바이러스 벡터의 수율을 25% 증가시켰습니다. 이는 제조 공정에 내장된 자동화 및 AI에 의해 더욱 촉진될 것입니다. 이를 통해 비용을 절감하고 스케일업을 단순화할 수 있습니다. 이는 유전자 치료용 임상용 바이러스 벡터에 대한 수요 증가에 대응하기 위해 필수적입니다.

규제 및 제조 과제

이러한 발전 전망에도 불구하고 바이러스 벡터 제조 시장은 여러 가지 도전에 직면해 있으며, 그 중 상당수는 규제 및 생산 규모 확대의 어려움과 관련이 있습니다. 2023년 기사에 따르면 바이러스 벡터를 이용한 치료법의 승인에 드는 기간이 점점 길어지고 있으며, 승인 절차에 따라는 3-5년의 시간이 소요될 수도 있다고 합니다. 또한 품질관리를 보장하면서 제조 중 오염물질에 대한 노출을 최소화하면서 스케일업하는 것은 큰 관심사 중 하나입니다. 이에 대해 FDA와 EMA를 비롯한 규제 당국은 업계 이해관계자들과 협력하여 바이러스 벡터 제조에 대한 보다 명확한 가이드라인을 마련하기 위해 노력하고 있습니다. 계속 변화하는 규제 상황은 생산 전략에 영향을 미치고, 시장 출시 기간을 지연시킬 수 있으며, 나아가 산업 전반의 성장에도 영향을 미칠 수 있습니다.

목차

제1장 서문

제2장 조사 범위와 조사 방법

제3장 개요

제4장 서론

제5장 세계의 바이러스 벡터 제조 시장

제6장 시장 내역 : 유형별

제7장 시장 내역 : 질환별

제8장 시장 내역 : 용도별

제9장 시장 내역 : 최종사용자별

제10장 시장 내역 : 지역별

제11장 SWOT 분석

제12장 밸류체인 분석

제13장 Porters Five Forces 분석

제14장 가격 분석

제15장 경쟁 구도

KSA 26.05.19

The global viral vector manufacturing market size was valued at USD 1,786.3 Million in 2025. Looking forward, IMARC Group estimates the market to reach USD 9,549.9 Million by 2034, exhibiting a CAGR of 19.86% from 2026-2034. North America currently dominates the market, holding a market share of over 49.3% in 2025. The rising prevalence of genetic disorders, increasing adoption of gene therapies, advanced biotechnology infrastructure, expanding clinical trials, strong government funding, robust R&D investments, and the presence of leading pharmaceutical companies drive the viral vector manufacturing market in North America.

The global viral vector manufacturing market is experiencing significant growth, driven by the increasing prevalence of genetic disorders and infectious diseases, coupled with advancements in gene and cell therapy. The growing adoption of viral vectors in the development of innovative therapies for rare diseases, cancer, and neurological disorders is a key factor boosting demand. Expanding clinical trials for gene therapies and rising government investments in biotechnology and pharmaceutical research are further supporting market expansion. Moreover, the development of scalable manufacturing technologies and improved production processes has boosted the efficiency and cost-effectiveness of viral vector production. Increasing collaborations between pharmaceutical companies and research institutions are also accelerating the development of novel therapies, further propelling the growth of the viral vector manufacturing market.

The United States is emerging as one of the key markets with 91.90% of the total market share, propelled by several key factors. A significant driver is the increasing prevalence of genetic disorders and cancers, which has intensified the demand for gene and cell therapies utilizing viral vectors. This growth is further supported by substantial government investments in biotechnology and the presence of numerous contract development and manufacturing organizations (CDMOs) in the country. Additionally, advancements in scalable manufacturing technologies have enhanced production efficiency, meeting the rising demand for viral vectors in therapeutic applications. The expanding pipeline of gene therapies and increasing clinical trials are also contributing to the market's expansion, positioning the U.S. as a leading hub for viral vector manufacturing.

VIRAL VECTOR MANUFACTURING MARKET TRENDS:

Market Growth and Investment

As of March 18, 2024, the FDA has approved 36 gene therapies. There are more than 500 in development. The agency predicts that, by 2025, it will approve around 10 to 20 products every year in gene therapy. The increase is fueled by a boost in biotechnology investment and new technologies being developed in the gene therapy arena. Proactivity by the FDA in regulating gene therapy has allowed a few of these treatment solutions to be fast-tracked and approved rapidly. The expected approvals annually represent the growing trust built for the safety and efficacy profiles of gene therapies. The actual number of approved gene therapies and the robust pipeline depict an active market poised for significant growth. This trend is set to continue; however, market expansion will significantly be driven by the commitment by the FDA toward innovative therapies. As a response to this increase, pharmaceutical firms are investing extensively in viral vector manufacturing to answer the growing demands of gene therapy. This is because a sustained supply of good quality viral vectors is essential in guaranteeing successful gene therapies. The FDA support and the industry investment in manufacturing infrastructure are critical to overcome the challenges of scaling up production. These efforts are meant to ensure that the benefits of gene therapies are accessible to a broader patient population.

Technological Advancements and Process Optimization

The growth in the market is driven by the technological advancement in viral vector manufacturing, such as cell line development and improvement in production processes. The stable packaging cell lines increase the efficiency of viral vector production, thereby fueling the growth of the market. For instance, the HEK293 cell line technology adopted by Samsung Biologics increased viral vector yield by 25% in 2022. This will be further facilitated by the automation and AI that is being incorporated into manufacturing processes. It lowers costs and simplifies scaling. This is necessary to meet the increased demand for clinical-grade viral vectors for gene therapies.

Regulatory and Manufacturing Challenges

Despite these development prospects, this viral vector manufacturing market is struggling with several issues, most of which involve regulating and the difficulties of scaling up production. According to a 2023 article, approval times for viral vector-based therapies are becoming increasingly lengthy, with approval processes sometimes taking as long as 3-5 years. Additionally, scaling up while ensuring quality control and minimizing contaminant exposures during manufacturing is one area of major concern. In response, the FDA and EMA, among other regulatory bodies, are engaging with industry stakeholders to establish clearer guidelines for the manufacturing of viral vectors. The evolving regulatory landscape will influence production strategies and could slow the time to market, thus affecting the overall growth of the industry.

VIRAL VECTOR MANUFACTURING INDUSTRY SEGMENTATION:

Analysis by Type:

  • Adenoviral Vectors
  • Adeno-associated Viral Vectors
  • Lentiviral Vectors
  • Retroviral Vectors
  • Others

In 2025, Adeno-associated viral (AAV) vectors emerge as the largest segment in the viral vector manufacturing market, driven by their versatility and safety profile. AAV vectors are frequently utilized in gene therapy due to their minimal immune response and their effectiveness in delivering therapeutic genes to specific target cells with precision. Their significant role in treating genetic disorders, such as spinal muscular atrophy (SMA) and inherited retinal diseases, has propelled their demand. The ongoing advancements in AAV vector engineering have further enhanced their efficiency, scalability, and therapeutic potential. Additionally, the increasing number of FDA-approved AAV-based therapies and the growing pipeline of clinical trials utilizing AAV vectors reinforce their dominance, making them a crucial component of the expanding gene therapy landscape.

Analysis by Disease:

  • Cancer
  • Genetic Disorders
  • Infectious Diseases
  • Others

In 2025, cancer emerged as the leading application segment in the viral vector manufacturing market, accounting for approximately 37.6% of the market share. The dominance of this segment is attributed to the growing adoption of viral vectors in gene therapies and oncolytic virotherapy for treating various types of cancer. Advances in immunotherapy, such as CAR-T cell therapies, which rely on viral vectors for genetic modifications, have further driven this growth. The growing global prevalence of cancer, along with increased investments in oncology research and clinical trials, has driven the demand for innovative treatment solutions. Furthermore, the approval of viral vector-based therapies for specific cancers highlights their efficacy, solidifying their role in transforming cancer treatment strategies globally.

Analysis by Application:

  • Gene Therapy
  • Vaccinology

In 2025, gene therapy dominated the viral vector manufacturing market, accounting for approximately 56.9% of the market share. This leadership is driven by the growing adoption of gene therapies to treat genetic disorders, cancers, and rare diseases. Viral vectors, especially adeno-associated viruses (AAV) and lentiviruses, play a crucial role in delivering therapeutic genes to target cells with accuracy and efficiency. The expanding pipeline of gene therapy candidates and increasing regulatory approvals have significantly boosted demand. Notable advancements in viral vector engineering and scalable manufacturing technologies further support this segment's growth. Additionally, rising investments from pharmaceutical companies and government initiatives aimed at advancing gene therapy research contribute to its prominence, positioning it as a transformative force in modern medicine.

Analysis by End User:

  • Pharmaceutical and Biopharmaceutical Companies
  • Research Institutes

Pharmaceutical and biopharmaceutical companies are the primary end-users in the viral vector manufacturing market. These companies drive demand due to their extensive use of viral vectors in gene and cell therapy development, clinical trials, and commercial-scale manufacturing. Rising investments in personalized medicine and innovative therapies further strengthen this segment's dominance.

Research institutes play a crucial role in the viral vector manufacturing market by fostering innovation and advancing preclinical studies. These institutes focus on developing novel therapies for genetic disorders, cancer, and rare diseases. Collaborations with pharmaceutical companies and increased government funding for biotechnology research further enhance their contribution to market growth.

Regional Analysis:

  • North America
    • United States
    • Canada
  • Asia-Pacific
    • China
    • Japan
    • India
    • South Korea
    • Australia
    • Indonesia
    • Others
  • Europe
    • Germany
    • France
    • United Kingdom
    • Italy
    • Spain
    • Russia
    • Others
  • Latin America
    • Brazil
    • Mexico
    • Others
  • Middle East and Africa

The market share in North America is seen to have crossed over 49.3% in the year 2025. The key factors that boosted the North America viral vector manufacturing market include a rapid growth rate of the aerospace and energy industries in North America, which are seen to be the largest consumers of viral vector manufacturings. Furthermore, a robust base of companies in the region has further promoted innovation and growth in the viral vector manufacturing market. In addition, North America has a strong research and development infrastructure, with many universities and research institutions conducting cutting-edge research in materials science and engineering, further driving the viral vector manufacturing market.

KEY REGIONAL TAKEAWAYS:

UNITED STATES VIRAL VECTOR MANUFACTURING MARKET ANALYSIS

The U.S. viral vector manufacturing market is growing fast as demand for gene therapies continues to increase along with advanced manufacturing technologies. In fact, as per a snapshot of global gene therapy trials, there were over 3,900 clinical trials across the world by March 2023, of which a majority was conducted in the United States, as per reports. The CHIPS and Science Act in 2022 gave authorization to USD 280 billion to advance U.S. scientific and technological research, some of which is aligning with advancements in biotechnology. Portfolio leaders, such as Thermo Fisher Scientific and Catalent, continue to add capacity in the United States to meet demand. Growth is driven by innovations in scalable production processes and federal incentives. This focus on quality and regulatory compliance helps strengthen U.S. leadership in viral vector manufacturing while exploiting export opportunities to improve its position globally in the biotech industry.

EUROPE VIRAL VECTOR MANUFACTURING MARKET ANALYSIS

The viral vector manufacturing market in Europe is growing as the investment in biotechnology and R&D funding is increasing. Horizon Europe, the European Union's leading research and innovation initiative, has designated EUR 11.5 billion (USD 12.6 billion) for the advancement of biotechnology and pharmaceutical research and development. InvestEU will also invest more than EUR 1 billion (USD 1.1 billion) in biotech and medicines-related investments, thus boosting innovation in vector production. BioNTech and Oxford Biomedica are some of the regional leaders in scalable manufacturing technologies. Strict regulatory frameworks by the EU guarantee the highest safety and quality standards for the production of cutting-edge therapies. Collaborative public-private partnerships and sustainable integration further boost Europe's position as a global hub for viral vector manufacturing, with strategic funding initiatives ensuring growth and technological advancement.

ASIA PACIFIC VIRAL VECTOR MANUFACTURING MARKET ANALYSIS

The Asia Pacific market for viral vector manufacturing is growing with a rapid speed as there has been an increasing investment in the field of biotechnology and governmental policies. As China's government invested heavily into the R&D in biotechnology, public R&D investment exceeded USD 3.8 billion from 2008 to 2020, as per reports, the commitment for advancements in gene therapy and viral vector technologies can be seen. The "Make in India" initiative by India and the regenerative medicine thrust by Japan are encouraging local manufacturing capabilities. Regional players such as WuXi AppTec and Samsung Biologics are exploiting partnerships to scale up and transfer technology. The growing clinical trials and need for cost-effective production solutions are making the region a major player in the global viral vector manufacturing market. Integration of new manufacturing technologies and supportive policies also fuels growth in the sector in Asia Pacific.

LATIN AMERICA VIRAL VECTOR MANUFACTURING MARKET ANALYSIS

The viral vector manufacturing market in Latin America is expected to expand in the upcoming years, fueled by higher investments in biotechnology and progress in gene therapy. GEMMABio has also recently announced a partnership with the health ministry in Brazil worth USD 100 million to introduce gene therapies for rare diseases into the country, taking a huge leap forward in accessing gene therapies across the region. Expanding its biotechnology sector, the industry will also grow at an estimated CAGR of 14.2% between 2024 and 2030 to help drive growing demand for manufacturing gene therapy in Brazil, as per an industry report. Strong biotechnology leadership from Brazil makes this strategic alliance position it strategically within Latin America's gene therapy and viral vector manufacturing market. Countries like Mexico and Argentina are also investing in local production capabilities and international collaborations, so Latin America will continue to strengthen its role in global biomanufacturing.

MIDDLE EAST AND AFRICA VIRAL VECTOR MANUFACTURING MARKET ANALYSIS

The viral vector manufacturing market in Middle East and Africa is growing by increasing healthcare spend and government interest in enhancing infrastructure of biotechnology. According to International Trade Administration (ITA), Saudi Arabia accounts for 60 percent of the Gulf Cooperation Council (GCC) countries' healthcare expenditure. In 2023, Saudi allocated USD 50.4 billion (16.96% of the budget) on healthcare and social development, emphasizing the importance and focus on biotechnology and the healthcare industries in the country. The Saudi Arabian Government is adopting healthcare privatization as part of Vision 2030, which includes significant investments into biotech and gene therapy manufacturing. This environment is making the region increasingly attractive to homegrown and foreign players alike and positions it well as a future hub for the manufacturing of viral vectors, as countries in the region seek to augment their self-sufficiency in advanced healthcare technologies.

COMPETITIVE LANDSCAPE:

The global viral vector manufacturing market is highly competitive, with leading companies focusing on technological advancements, expanding their production capabilities, and forming strategic partnerships to strengthen their market standing. Major companies dominate the market with extensive expertise and robust production capabilities. These firms invest heavily in R&D to enhance vector engineering, scalability, and manufacturing efficiency. Emerging players and contract development and manufacturing organizations (CDMOs) are also gaining traction by offering cost-effective solutions and specialized services. Partnerships between pharmaceutical companies, research institutes, and vector manufacturers are increasingly common, aimed at accelerating gene therapy development and commercialization. The competitive environment is also influenced by regional companies expanding their operations to address the increasing global demand for viral vectors.

The report provides a comprehensive analysis of the competitive landscape in the viral vector manufacturing market with detailed profiles of all major companies, including:

  • Aldevron LLC
  • Catalent, Inc
  • Charles River Laboratories International Inc.
  • Cytiva (Danaher Corporation)
  • F. Hoffmann-La Roche Ltd
  • FUJIFILM Diosynth Biotechnologies
  • Genezen
  • Kaneka Corporation
  • Lonza
  • Merck KGaA
  • Oxford Biomedica PLC
  • Thermo Fisher Scientific Inc.

Table of Contents

1 Preface

2 Scope and Methodology

  • 2.1 Objectives of the Study
  • 2.2 Stakeholders
  • 2.3 Data Sources
    • 2.3.1 Primary Sources
    • 2.3.2 Secondary Sources
  • 2.4 Market Estimation
    • 2.4.1 Bottom-Up Approach
    • 2.4.2 Top-Down Approach
  • 2.5 Forecasting Methodology

3 Executive Summary

4 Introduction

  • 4.1 Overview
  • 4.2 Key Industry Trends

5 Global Viral Vector Manufacturing Market

  • 5.1 Market Overview
  • 5.2 Market Performance
  • 5.3 Impact of COVID-19
  • 5.4 Market Forecast

6 Market Breakup by Type

  • 6.1 Adenoviral Vectors
    • 6.1.1 Market Trends
    • 6.1.2 Market Forecast
  • 6.2 Adeno-associated Viral Vectors
    • 6.2.1 Market Trends
    • 6.2.2 Market Forecast
  • 6.3 Lentiviral Vectors
    • 6.3.1 Market Trends
    • 6.3.2 Market Forecast
  • 6.4 Retroviral Vectors
    • 6.4.1 Market Trends
    • 6.4.2 Market Forecast
  • 6.5 Others
    • 6.5.1 Market Trends
    • 6.5.2 Market Forecast

7 Market Breakup by Disease

  • 7.1 Cancer
    • 7.1.1 Market Trends
    • 7.1.2 Market Forecast
  • 7.2 Genetic Disorders
    • 7.2.1 Market Trends
    • 7.2.2 Market Forecast
  • 7.3 Infectious Diseases
    • 7.3.1 Market Trends
    • 7.3.2 Market Forecast
  • 7.4 Others
    • 7.4.1 Market Trends
    • 7.4.2 Market Forecast

8 Market Breakup by Application

  • 8.1 Gene Therapy
    • 8.1.1 Market Trends
    • 8.1.2 Market Forecast
  • 8.2 Vaccinology
    • 8.2.1 Market Trends
    • 8.2.2 Market Forecast

9 Market Breakup by End User

  • 9.1 Pharmaceutical and Biopharmaceutical Companies
    • 9.1.1 Market Trends
    • 9.1.2 Market Forecast
  • 9.2 Research Institutes
    • 9.2.1 Market Trends
    • 9.2.2 Market Forecast

10 Market Breakup by Region

  • 10.1 North America
    • 10.1.1 United States
      • 10.1.1.1 Market Trends
      • 10.1.1.2 Market Forecast
    • 10.1.2 Canada
      • 10.1.2.1 Market Trends
      • 10.1.2.2 Market Forecast
  • 10.2 Asia-Pacific
    • 10.2.1 China
      • 10.2.1.1 Market Trends
      • 10.2.1.2 Market Forecast
    • 10.2.2 Japan
      • 10.2.2.1 Market Trends
      • 10.2.2.2 Market Forecast
    • 10.2.3 India
      • 10.2.3.1 Market Trends
      • 10.2.3.2 Market Forecast
    • 10.2.4 South Korea
      • 10.2.4.1 Market Trends
      • 10.2.4.2 Market Forecast
    • 10.2.5 Australia
      • 10.2.5.1 Market Trends
      • 10.2.5.2 Market Forecast
    • 10.2.6 Indonesia
      • 10.2.6.1 Market Trends
      • 10.2.6.2 Market Forecast
    • 10.2.7 Others
      • 10.2.7.1 Market Trends
      • 10.2.7.2 Market Forecast
  • 10.3 Europe
    • 10.3.1 Germany
      • 10.3.1.1 Market Trends
      • 10.3.1.2 Market Forecast
    • 10.3.2 France
      • 10.3.2.1 Market Trends
      • 10.3.2.2 Market Forecast
    • 10.3.3 United Kingdom
      • 10.3.3.1 Market Trends
      • 10.3.3.2 Market Forecast
    • 10.3.4 Italy
      • 10.3.4.1 Market Trends
      • 10.3.4.2 Market Forecast
    • 10.3.5 Spain
      • 10.3.5.1 Market Trends
      • 10.3.5.2 Market Forecast
    • 10.3.6 Russia
      • 10.3.6.1 Market Trends
      • 10.3.6.2 Market Forecast
    • 10.3.7 Others
      • 10.3.7.1 Market Trends
      • 10.3.7.2 Market Forecast
  • 10.4 Latin America
    • 10.4.1 Brazil
      • 10.4.1.1 Market Trends
      • 10.4.1.2 Market Forecast
    • 10.4.2 Mexico
      • 10.4.2.1 Market Trends
      • 10.4.2.2 Market Forecast
    • 10.4.3 Others
      • 10.4.3.1 Market Trends
      • 10.4.3.2 Market Forecast
  • 10.5 Middle East and Africa
    • 10.5.1 Market Trends
    • 10.5.2 Market Breakup by Country
    • 10.5.3 Market Forecast

11 SWOT Analysis

  • 11.1 Overview
  • 11.2 Strengths
  • 11.3 Weaknesses
  • 11.4 Opportunities
  • 11.5 Threats

12 Value Chain Analysis

13 Porters Five Forces Analysis

  • 13.1 Overview
  • 13.2 Bargaining Power of Buyers
  • 13.3 Bargaining Power of Suppliers
  • 13.4 Degree of Competition
  • 13.5 Threat of New Entrants
  • 13.6 Threat of Substitutes

14 Price Analysis

15 Competitive Landscape

  • 15.1 Market Structure
  • 15.2 Key Players
  • 15.3 Profiles of Key Players
    • 15.3.1 Aldevron LLC
      • 15.3.1.1 Company Overview
      • 15.3.1.2 Product Portfolio
      • 15.3.1.3 Financials
      • 15.3.1.4 SWOT Analysis
    • 15.3.2 Catalent, Inc
      • 15.3.2.1 Company Overview
      • 15.3.2.2 Product Portfolio
      • 15.3.2.3 Financials
      • 15.3.2.4 SWOT Analysis
    • 15.3.3 Charles River Laboratories International Inc.
      • 15.3.3.1 Company Overview
      • 15.3.3.2 Product Portfolio
    • 15.3.4 Cytiva (Danaher Corporation)
      • 15.3.4.1 Company Overview
      • 15.3.4.2 Product Portfolio
      • 15.3.4.3 Financials
      • 15.3.4.4 SWOT Analysis
    • 15.3.5 F. Hoffmann-La Roche Ltd
      • 15.3.5.1 Company Overview
      • 15.3.5.2 Product Portfolio
      • 15.3.5.3 Financials
    • 15.3.6 FUJIFILM Diosynth Biotechnologies
      • 15.3.6.1 Company Overview
      • 15.3.6.2 Product Portfolio
      • 15.3.6.3 Financials
      • 15.3.6.4 SWOT Analysis
    • 15.3.7 Genezen
      • 15.3.7.1 Company Overview
      • 15.3.7.2 Product Portfolio
      • 15.3.7.3 Financials
      • 15.3.7.4 SWOT Analysis
    • 15.3.8 Kaneka Corporation
      • 15.3.8.1 Company Overview
      • 15.3.8.2 Product Portfolio
    • 15.3.9 Lonza
      • 15.3.9.1 Company Overview
      • 15.3.9.2 Product Portfolio
      • 15.3.9.3 Financials
      • 15.3.9.4 SWOT Analysis
    • 15.3.10 Merck KGaA
      • 15.3.10.1 Company Overview
      • 15.3.10.2 Product Portfolio
      • 15.3.10.3 Financials
      • 15.3.10.4 SWOT Analysis
    • 15.3.11 Oxford Biomedica PLC
      • 15.3.11.1 Company Overview
      • 15.3.11.2 Product Portfolio
      • 15.3.11.3 Financials
      • 15.3.11.4 SWOT Analysis
    • 15.3.12 Thermo Fisher Scientific Inc.
      • 15.3.12.1 Company Overview
      • 15.3.12.2 Product Portfolio
      • 15.3.12.3 Financials
      • 15.3.12.4 SWOT Analysis
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