AAV Packaging Service Market by Container Type (Cartridges, Syringes, Vials), Packaging Material (Cyclic Olefin Polymer, Glass, Plastic), Scale, Delivery Format, Application, End User - Global Forecast 2026-2032
Description
The AAV Packaging Service Market was valued at USD 1.92 billion in 2025 and is projected to grow to USD 2.02 billion in 2026, with a CAGR of 5.43%, reaching USD 2.79 billion by 2032.
A comprehensive introductory framing that explains why packaging strategy is now central to AAV program success, regulatory readiness, and patient outcomes
The emergence of adeno-associated virus (AAV) as a leading vector for gene therapies has elevated the role of packaging services from a technical consideration to a strategic capability for developers and manufacturers. Packaging decisions now influence not only product stability but also regulatory compliance, cold-chain logistics, and patient-facing administration modalities. As clinical pipelines expand and trial complexity rises, organizations must view packaging as an integrated part of their development and commercialization strategy rather than an afterthought.
This executive summary synthesizes the key forces reshaping AAV packaging services and highlights how stakeholders can respond to operational, regulatory, and commercial pressures. The opening section establishes the context for subsequent analysis by outlining the critical intersections between container formats, delivery states, end-user needs, and scale considerations. It also sets expectations for actionable insights, emphasizing pragmatic recommendations for aligning packaging choices with clinical and commercial objectives while maintaining quality and supply chain resilience.
An authoritative examination of the transformative technological, regulatory, and supply chain shifts that are redefining AAV packaging strategies across the therapy lifecycle
The landscape for AAV packaging is undergoing transformative shifts driven by scientific progress, supply chain reconfiguration, regulatory refinement, and heightened focus on patient-centric delivery. Advances in vector engineering and dose optimization have intensified demand for delivery formats that preserve potency and enable precise dosing at point of care, pushing suppliers to innovate on materials and handling systems.
Concurrently, manufacturing strategies are pivoting toward greater partnership models and modular supply networks, which emphasize the need for standardized packaging interfaces that can be qualified across multiple contract development and manufacturing organizations. Regulatory pathways are tightening expectations for container-closure integrity, extractables and leachables characterization, and cold-chain validation, prompting early-stage developers to incorporate packaging qualification into clinical transition planning. Taken together, these shifts create a landscape where packaging is both a risk area and a differentiator, with forward-looking organizations investing in configurable solutions that can support diverse delivery volumes and regulatory territories.
A detailed assessment of how the cumulative tariff changes enacted in 2025 are reshaping supplier selection, sourcing strategies, and packaging qualification priorities for AAV programs
Policy changes and tariff adjustments implemented in 2025 have layered new considerations into supplier selection, cost structures, and supply chain routing for companies reliant on cross-border sourcing of packaging components and materials. The cumulative impact of these tariff measures has prompted stakeholders to reassess sourcing strategies for primary packaging such as glass and polymer components, and for ancillary items used in cold-chain and aseptic handling.
In response, many organizations are exploring regional supplier diversification and nearshoring to reduce exposure to tariff volatility and to shorten lead times. This movement drives a re-evaluation of qualification timelines, as qualifying alternative vendors requires rigorous comparability testing for container-closure systems and compatibility studies with drug product. Moreover, the tariff environment has elevated the importance of lifecycle cost analysis that incorporates reliability, logistics complexity, and regulatory acceptability rather than focusing solely on unit price. As a result, procurement teams are collaborating more closely with regulatory and quality functions to ensure that any shift in sourcing preserves product integrity and compliance.
A nuanced segmentation-driven perspective that explains how container types, delivery formats, end users, applications, materials, and scale each shape packaging strategy and risk management
Effective segmentation illuminates how packaging requirements diverge across container types, delivery formats, end users, applications, materials, and operational scale, enabling targeted strategies that reflect distinct technical constraints and commercial imperatives. When examined by container type, the market shows distinct pathways for cartridges, syringes, and vials; cartridges split into reusable and single-use variants, syringes separate into pre-filled and standard approaches, and vials are differentiated by multi-dose and single-dose configurations. These distinctions drive choices around fill-finish automation, container-closure validation, and human factors considerations for administration.
Delivery format further bifurcates needs between liquid and lyophilized presentations, with lyophilization introducing unique questions about cycle development, excipient compatibility, and stability testing. End-user segmentation highlights differing priorities among biotech companies, CDMOs, and pharmaceutical companies, each balancing speed to clinic, scale-up predictability, and cost control in different ways. Application-focused segmentation spans clinical trials, gene therapy programs, and research use, and clinical trials themselves require nuanced planning across Phase I, Phase II, and Phase III stages where dosing regimens, batch sizes, and regulatory evidence expectations evolve. Packaging material choices are another critical axis; cyclic olefin polymer, glass, and plastic each offer trade-offs for breakage risk, extractables and leachables profiles, and compatibility with cold-chain requirements, while plastic options subdivide into HDPE and LDPE with distinct mechanical and barrier properties. Finally, scale considerations separate clinical scale activities from commercial scale manufacturing, dictating different validation approaches, supplier contracts, and inventory strategies. Taken together, these segmentation lenses provide a framework for aligning packaging design, supplier partnerships, and quality systems with program-specific risk tolerances and timelines.
A strategic regional analysis that contrasts logistics, regulatory complexity, and supplier ecosystems across the Americas, Europe Middle East & Africa, and Asia-Pacific to guide sourcing decisions
Regional dynamics exert a profound influence on packaging sourcing, regulatory expectations, and logistics complexity, and understanding those differences is essential for resilient program planning. In the Americas, proximity to major development hubs supports rapid iteration and close collaboration between developers and packaging suppliers, yet complex cross-border regulatory harmonization and infrastructure variability can affect cold-chain continuity and customs clearance strategies.
In Europe, the Middle East & Africa region, highly harmonized regulatory frameworks in many European jurisdictions coexist with divergent requirements in other territories, prompting companies to adopt flexible qualification strategies and to invest in targeted regulatory dossiers for local acceptability. The Asia-Pacific region presents opportunities for manufacturing scale and component supply diversification, but it also requires careful navigation of regional standards, import controls, and supplier governance to ensure that container-closure systems meet global safety expectations. Across all regions, logistics network design, warehousing capabilities for temperature-sensitive goods, and local regulatory interactions determine the speed and reliability with which clinical and commercial programs can be executed, making geographic strategy a core element of packaging planning.
Insightful analysis of company-level behaviors showing how integrated analytical services, modular fill-finish platforms, and collaborative qualification approaches are redefining supplier value
Key company behaviors reveal patterns that organizations can learn from when selecting partners or benchmarking internal capabilities. Leading suppliers and contract manufacturers are differentiating through deeper integration of analytical services, accelerated container-closure testing regimes, and modular fill-finish platforms that can switch between cartridges, syringes, and vials with minimal requalification. These capabilities reduce time-to-clinic for developers while enabling scale-up continuity.
Meanwhile, biopharma firms and specialized CDMOs are investing in joint development agreements and co-qualification programs to secure manufacturing slots and to share the burden of packaging validation. There is also increased emphasis on partnerships that offer end-to-end traceability and serialization services to support regulatory labeling expectations and to enhance pharmacovigilance. Across the competitive landscape, companies that combine materials science expertise with regulatory acumen and robust supply chain orchestration are positioned to offer the most compelling value proposition for high-complexity AAV programs.
Practical and prioritized recommendations that enable industry leaders to reduce risk, accelerate clinical timelines, and optimize packaging strategies for AAV programs
Industry leaders can translate these insights into concrete actions that reduce program risk and accelerate development timelines. First, embed packaging qualification activities early in clinical development planning so that container-closure decisions are validated alongside formulation and process development, avoiding late-stage surprises. Second, diversify supplier bases across regions with an emphasis on qualifying alternate vendors in parallel, which reduces dependency on single points of failure and mitigates exposure to tariff-driven disruptions.
Third, standardize interfaces and adopt modular fill-finish solutions where feasible to shorten changeover times and to support flexible scaling between clinical and commercial phases. Fourth, prioritize materials and designs that minimize extractables and leachables risk, and invest in comprehensive stability and compatibility programs that will satisfy both regulatory reviewers and downstream clinical operations. Finally, strengthen cross-functional governance between procurement, quality, regulatory, and R&D teams to ensure that packaging decisions balance cost, compliance, and clinical practicality, thereby improving time-to-patient and long-term supply reliability.
A transparent and reproducible research methodology integrating expert interviews, regulatory review, and comparative case studies to validate packaging insights and recommendations
The research underpinning these insights combined qualitative expert interviews, document analysis of public regulatory guidance, and a structured review of technical literature focused on container-closure systems, extractables and leachables science, and cold-chain management. Interviews were conducted with packaging engineers, quality assurance leaders, and supply chain managers across development-stage companies, contract manufacturers, and component suppliers to surface operational challenges and emerging best practices.
Complementing stakeholder interviews, the methodology included cross-regional analysis of regulatory frameworks and trade policy changes, with a particular emphasis on how tariff adjustments influence sourcing behavior. Comparative case studies illustrated how different packaging materials and delivery formats perform under real-world manufacturing and distribution constraints, while triangulation of findings ensured that recommendations reflect pragmatic pathways for maintaining product integrity and regulatory compliance. The research approach prioritized reproducibility and transparency, enabling readers to trace conclusions back to the underlying evidence base and to adopt tailored solutions for their specific programs.
A concise concluding synthesis underscoring packaging as a strategic enabler for product integrity, regulatory success, and reliable patient access in AAV therapy programs
In conclusion, packaging for AAV therapies has moved from a tactical task to a strategic enabler that directly influences product quality, regulatory acceptance, and patient access. The interplay between container formats, delivery states, materials, and scale requires coordinated planning across technical and commercial functions, and the 2025 policy environment underscores the importance of resilient sourcing and supplier qualification strategies.
Organizations that proactively integrate packaging qualification into development roadmaps, diversify supply chains across regions, and partner with suppliers offering advanced analytical and modular fill-finish capabilities will be better positioned to navigate complexity and to deliver therapies to patients efficiently. Ultimately, disciplined packaging strategy is a differentiator that protects product integrity, supports regulatory confidence, and accelerates the path from clinic to commercialization.
Note: PDF & Excel + Online Access - 1 Year
A comprehensive introductory framing that explains why packaging strategy is now central to AAV program success, regulatory readiness, and patient outcomes
The emergence of adeno-associated virus (AAV) as a leading vector for gene therapies has elevated the role of packaging services from a technical consideration to a strategic capability for developers and manufacturers. Packaging decisions now influence not only product stability but also regulatory compliance, cold-chain logistics, and patient-facing administration modalities. As clinical pipelines expand and trial complexity rises, organizations must view packaging as an integrated part of their development and commercialization strategy rather than an afterthought.
This executive summary synthesizes the key forces reshaping AAV packaging services and highlights how stakeholders can respond to operational, regulatory, and commercial pressures. The opening section establishes the context for subsequent analysis by outlining the critical intersections between container formats, delivery states, end-user needs, and scale considerations. It also sets expectations for actionable insights, emphasizing pragmatic recommendations for aligning packaging choices with clinical and commercial objectives while maintaining quality and supply chain resilience.
An authoritative examination of the transformative technological, regulatory, and supply chain shifts that are redefining AAV packaging strategies across the therapy lifecycle
The landscape for AAV packaging is undergoing transformative shifts driven by scientific progress, supply chain reconfiguration, regulatory refinement, and heightened focus on patient-centric delivery. Advances in vector engineering and dose optimization have intensified demand for delivery formats that preserve potency and enable precise dosing at point of care, pushing suppliers to innovate on materials and handling systems.
Concurrently, manufacturing strategies are pivoting toward greater partnership models and modular supply networks, which emphasize the need for standardized packaging interfaces that can be qualified across multiple contract development and manufacturing organizations. Regulatory pathways are tightening expectations for container-closure integrity, extractables and leachables characterization, and cold-chain validation, prompting early-stage developers to incorporate packaging qualification into clinical transition planning. Taken together, these shifts create a landscape where packaging is both a risk area and a differentiator, with forward-looking organizations investing in configurable solutions that can support diverse delivery volumes and regulatory territories.
A detailed assessment of how the cumulative tariff changes enacted in 2025 are reshaping supplier selection, sourcing strategies, and packaging qualification priorities for AAV programs
Policy changes and tariff adjustments implemented in 2025 have layered new considerations into supplier selection, cost structures, and supply chain routing for companies reliant on cross-border sourcing of packaging components and materials. The cumulative impact of these tariff measures has prompted stakeholders to reassess sourcing strategies for primary packaging such as glass and polymer components, and for ancillary items used in cold-chain and aseptic handling.
In response, many organizations are exploring regional supplier diversification and nearshoring to reduce exposure to tariff volatility and to shorten lead times. This movement drives a re-evaluation of qualification timelines, as qualifying alternative vendors requires rigorous comparability testing for container-closure systems and compatibility studies with drug product. Moreover, the tariff environment has elevated the importance of lifecycle cost analysis that incorporates reliability, logistics complexity, and regulatory acceptability rather than focusing solely on unit price. As a result, procurement teams are collaborating more closely with regulatory and quality functions to ensure that any shift in sourcing preserves product integrity and compliance.
A nuanced segmentation-driven perspective that explains how container types, delivery formats, end users, applications, materials, and scale each shape packaging strategy and risk management
Effective segmentation illuminates how packaging requirements diverge across container types, delivery formats, end users, applications, materials, and operational scale, enabling targeted strategies that reflect distinct technical constraints and commercial imperatives. When examined by container type, the market shows distinct pathways for cartridges, syringes, and vials; cartridges split into reusable and single-use variants, syringes separate into pre-filled and standard approaches, and vials are differentiated by multi-dose and single-dose configurations. These distinctions drive choices around fill-finish automation, container-closure validation, and human factors considerations for administration.
Delivery format further bifurcates needs between liquid and lyophilized presentations, with lyophilization introducing unique questions about cycle development, excipient compatibility, and stability testing. End-user segmentation highlights differing priorities among biotech companies, CDMOs, and pharmaceutical companies, each balancing speed to clinic, scale-up predictability, and cost control in different ways. Application-focused segmentation spans clinical trials, gene therapy programs, and research use, and clinical trials themselves require nuanced planning across Phase I, Phase II, and Phase III stages where dosing regimens, batch sizes, and regulatory evidence expectations evolve. Packaging material choices are another critical axis; cyclic olefin polymer, glass, and plastic each offer trade-offs for breakage risk, extractables and leachables profiles, and compatibility with cold-chain requirements, while plastic options subdivide into HDPE and LDPE with distinct mechanical and barrier properties. Finally, scale considerations separate clinical scale activities from commercial scale manufacturing, dictating different validation approaches, supplier contracts, and inventory strategies. Taken together, these segmentation lenses provide a framework for aligning packaging design, supplier partnerships, and quality systems with program-specific risk tolerances and timelines.
A strategic regional analysis that contrasts logistics, regulatory complexity, and supplier ecosystems across the Americas, Europe Middle East & Africa, and Asia-Pacific to guide sourcing decisions
Regional dynamics exert a profound influence on packaging sourcing, regulatory expectations, and logistics complexity, and understanding those differences is essential for resilient program planning. In the Americas, proximity to major development hubs supports rapid iteration and close collaboration between developers and packaging suppliers, yet complex cross-border regulatory harmonization and infrastructure variability can affect cold-chain continuity and customs clearance strategies.
In Europe, the Middle East & Africa region, highly harmonized regulatory frameworks in many European jurisdictions coexist with divergent requirements in other territories, prompting companies to adopt flexible qualification strategies and to invest in targeted regulatory dossiers for local acceptability. The Asia-Pacific region presents opportunities for manufacturing scale and component supply diversification, but it also requires careful navigation of regional standards, import controls, and supplier governance to ensure that container-closure systems meet global safety expectations. Across all regions, logistics network design, warehousing capabilities for temperature-sensitive goods, and local regulatory interactions determine the speed and reliability with which clinical and commercial programs can be executed, making geographic strategy a core element of packaging planning.
Insightful analysis of company-level behaviors showing how integrated analytical services, modular fill-finish platforms, and collaborative qualification approaches are redefining supplier value
Key company behaviors reveal patterns that organizations can learn from when selecting partners or benchmarking internal capabilities. Leading suppliers and contract manufacturers are differentiating through deeper integration of analytical services, accelerated container-closure testing regimes, and modular fill-finish platforms that can switch between cartridges, syringes, and vials with minimal requalification. These capabilities reduce time-to-clinic for developers while enabling scale-up continuity.
Meanwhile, biopharma firms and specialized CDMOs are investing in joint development agreements and co-qualification programs to secure manufacturing slots and to share the burden of packaging validation. There is also increased emphasis on partnerships that offer end-to-end traceability and serialization services to support regulatory labeling expectations and to enhance pharmacovigilance. Across the competitive landscape, companies that combine materials science expertise with regulatory acumen and robust supply chain orchestration are positioned to offer the most compelling value proposition for high-complexity AAV programs.
Practical and prioritized recommendations that enable industry leaders to reduce risk, accelerate clinical timelines, and optimize packaging strategies for AAV programs
Industry leaders can translate these insights into concrete actions that reduce program risk and accelerate development timelines. First, embed packaging qualification activities early in clinical development planning so that container-closure decisions are validated alongside formulation and process development, avoiding late-stage surprises. Second, diversify supplier bases across regions with an emphasis on qualifying alternate vendors in parallel, which reduces dependency on single points of failure and mitigates exposure to tariff-driven disruptions.
Third, standardize interfaces and adopt modular fill-finish solutions where feasible to shorten changeover times and to support flexible scaling between clinical and commercial phases. Fourth, prioritize materials and designs that minimize extractables and leachables risk, and invest in comprehensive stability and compatibility programs that will satisfy both regulatory reviewers and downstream clinical operations. Finally, strengthen cross-functional governance between procurement, quality, regulatory, and R&D teams to ensure that packaging decisions balance cost, compliance, and clinical practicality, thereby improving time-to-patient and long-term supply reliability.
A transparent and reproducible research methodology integrating expert interviews, regulatory review, and comparative case studies to validate packaging insights and recommendations
The research underpinning these insights combined qualitative expert interviews, document analysis of public regulatory guidance, and a structured review of technical literature focused on container-closure systems, extractables and leachables science, and cold-chain management. Interviews were conducted with packaging engineers, quality assurance leaders, and supply chain managers across development-stage companies, contract manufacturers, and component suppliers to surface operational challenges and emerging best practices.
Complementing stakeholder interviews, the methodology included cross-regional analysis of regulatory frameworks and trade policy changes, with a particular emphasis on how tariff adjustments influence sourcing behavior. Comparative case studies illustrated how different packaging materials and delivery formats perform under real-world manufacturing and distribution constraints, while triangulation of findings ensured that recommendations reflect pragmatic pathways for maintaining product integrity and regulatory compliance. The research approach prioritized reproducibility and transparency, enabling readers to trace conclusions back to the underlying evidence base and to adopt tailored solutions for their specific programs.
A concise concluding synthesis underscoring packaging as a strategic enabler for product integrity, regulatory success, and reliable patient access in AAV therapy programs
In conclusion, packaging for AAV therapies has moved from a tactical task to a strategic enabler that directly influences product quality, regulatory acceptance, and patient access. The interplay between container formats, delivery states, materials, and scale requires coordinated planning across technical and commercial functions, and the 2025 policy environment underscores the importance of resilient sourcing and supplier qualification strategies.
Organizations that proactively integrate packaging qualification into development roadmaps, diversify supply chains across regions, and partner with suppliers offering advanced analytical and modular fill-finish capabilities will be better positioned to navigate complexity and to deliver therapies to patients efficiently. Ultimately, disciplined packaging strategy is a differentiator that protects product integrity, supports regulatory confidence, and accelerates the path from clinic to commercialization.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
182 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Definition
- 1.3. Market Segmentation & Coverage
- 1.4. Years Considered for the Study
- 1.5. Currency Considered for the Study
- 1.6. Language Considered for the Study
- 1.7. Key Stakeholders
- 2. Research Methodology
- 2.1. Introduction
- 2.2. Research Design
- 2.2.1. Primary Research
- 2.2.2. Secondary Research
- 2.3. Research Framework
- 2.3.1. Qualitative Analysis
- 2.3.2. Quantitative Analysis
- 2.4. Market Size Estimation
- 2.4.1. Top-Down Approach
- 2.4.2. Bottom-Up Approach
- 2.5. Data Triangulation
- 2.6. Research Outcomes
- 2.7. Research Assumptions
- 2.8. Research Limitations
- 3. Executive Summary
- 3.1. Introduction
- 3.2. CXO Perspective
- 3.3. Market Size & Growth Trends
- 3.4. Market Share Analysis, 2025
- 3.5. FPNV Positioning Matrix, 2025
- 3.6. New Revenue Opportunities
- 3.7. Next-Generation Business Models
- 3.8. Industry Roadmap
- 4. Market Overview
- 4.1. Introduction
- 4.2. Industry Ecosystem & Value Chain Analysis
- 4.2.1. Supply-Side Analysis
- 4.2.2. Demand-Side Analysis
- 4.2.3. Stakeholder Analysis
- 4.3. Porter’s Five Forces Analysis
- 4.4. PESTLE Analysis
- 4.5. Market Outlook
- 4.5.1. Near-Term Market Outlook (0–2 Years)
- 4.5.2. Medium-Term Market Outlook (3–5 Years)
- 4.5.3. Long-Term Market Outlook (5–10 Years)
- 4.6. Go-to-Market Strategy
- 5. Market Insights
- 5.1. Consumer Insights & End-User Perspective
- 5.2. Consumer Experience Benchmarking
- 5.3. Opportunity Mapping
- 5.4. Distribution Channel Analysis
- 5.5. Pricing Trend Analysis
- 5.6. Regulatory Compliance & Standards Framework
- 5.7. ESG & Sustainability Analysis
- 5.8. Disruption & Risk Scenarios
- 5.9. Return on Investment & Cost-Benefit Analysis
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. AAV Packaging Service Market, by Container Type
- 8.1. Cartridges
- 8.1.1. Reusable
- 8.1.2. Single Use
- 8.2. Syringes
- 8.2.1. Pre Filled
- 8.2.2. Standard
- 8.3. Vials
- 8.3.1. Multi Dose
- 8.3.2. Single Dose
- 9. AAV Packaging Service Market, by Packaging Material
- 9.1. Cyclic Olefin Polymer
- 9.2. Glass
- 9.3. Plastic
- 9.3.1. HDPE
- 9.3.2. LDPE
- 10. AAV Packaging Service Market, by Scale
- 10.1. Clinical Scale
- 10.2. Commercial Scale
- 11. AAV Packaging Service Market, by Delivery Format
- 11.1. Liquid
- 11.2. Lyophilized
- 12. AAV Packaging Service Market, by Application
- 12.1. Clinical Trials
- 12.1.1. Phase I
- 12.1.2. Phase II
- 12.1.3. Phase III
- 12.2. Gene Therapy
- 12.3. Research Use
- 13. AAV Packaging Service Market, by End User
- 13.1. Biotech Companies
- 13.2. CDMOs
- 13.3. Pharma Companies
- 14. AAV Packaging Service Market, by Region
- 14.1. Americas
- 14.1.1. North America
- 14.1.2. Latin America
- 14.2. Europe, Middle East & Africa
- 14.2.1. Europe
- 14.2.2. Middle East
- 14.2.3. Africa
- 14.3. Asia-Pacific
- 15. AAV Packaging Service Market, by Group
- 15.1. ASEAN
- 15.2. GCC
- 15.3. European Union
- 15.4. BRICS
- 15.5. G7
- 15.6. NATO
- 16. AAV Packaging Service Market, by Country
- 16.1. United States
- 16.2. Canada
- 16.3. Mexico
- 16.4. Brazil
- 16.5. United Kingdom
- 16.6. Germany
- 16.7. France
- 16.8. Russia
- 16.9. Italy
- 16.10. Spain
- 16.11. China
- 16.12. India
- 16.13. Japan
- 16.14. Australia
- 16.15. South Korea
- 17. United States AAV Packaging Service Market
- 18. China AAV Packaging Service Market
- 19. Competitive Landscape
- 19.1. Market Concentration Analysis, 2025
- 19.1.1. Concentration Ratio (CR)
- 19.1.2. Herfindahl Hirschman Index (HHI)
- 19.2. Recent Developments & Impact Analysis, 2025
- 19.3. Product Portfolio Analysis, 2025
- 19.4. Benchmarking Analysis, 2025
- 19.5. AGC Biologics, Inc.
- 19.6. Aldevron, LLC
- 19.7. Catalent, Inc.
- 19.8. Charles River Laboratories International, Inc.
- 19.9. FUJIFILM Diosynth Biotechnologies U.S.A., Inc.
- 19.10. Genezen Laboratories, Inc.
- 19.11. Lonza Group AG
- 19.12. Novasep Holding SAS
- 19.13. Oxford Biomedica plc
- 19.14. Samsung Biologics Co., Ltd.
- 19.15. The Center for Breakthrough Medicines, LLC
- 19.16. Thermo Fisher Scientific, Inc.
- 19.17. Vector BioMed, Inc.
- 19.18. Vigene Biosciences, Inc.
- 19.19. WuXi AppTec Co., Ltd.
- 19.20. Yposkesi SAS
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