Meningococcal Vaccines Market by Vaccine Type (Conjugate, Polysaccharide, Protein Subunit), Age Group (Adolescent, Adult, Geriatric), Formulation, Distribution Channel, End User, Indication - Global Forecast 2025-2032
Description
The Meningococcal Vaccines Market was valued at USD 5.95 billion in 2024 and is projected to grow to USD 6.60 billion in 2025, with a CAGR of 11.03%, reaching USD 13.74 billion by 2032.
A concise framing of the contemporary meningococcal vaccine landscape connecting immunology advances with deployment, policy drivers, and operational priorities
Meningococcal disease remains a persistent public health challenge due to its rapid onset and potentially severe outcomes, and stakeholders require a clear, operationally focused synthesis of current vaccine modalities, delivery systems, and policy drivers. This executive summary synthesizes recent advances in conjugate and protein subunit immunology, evolving immunization schedules across age cohorts, and the logistical imperatives that now shape procurement decisions. It further contextualizes how distribution channels, clinical end users, and indication-specific requirements converge to inform deployment strategies in routine and emergency settings.
The introduction frames the landscape by connecting scientific progress with real-world programmatic constraints. It highlights how vaccine formulation choices influence cold-chain logistics, dose-sparing strategies, and post-marketing surveillance, while also noting that demographic targeting-spanning pediatric immunization programs through geriatric and traveler cohorts-affects uptake and resource allocation. Finally, the introduction outlines the principal analytic lenses used throughout the report, emphasizing readiness for outbreak response, resilience of supply chains, and the strategic interplay between public health objectives and commercial imperatives.
How scientific, regulatory, and distribution innovations are reshaping product development, procurement strategies, and outbreak preparedness across the sector
The meningococcal vaccine landscape is undergoing transformative shifts driven by scientific innovation, regulatory evolution, and new delivery paradigms that together change how stakeholders plan and invest. Advances in protein subunit vaccines and improvements to conjugate chemistry are expanding protective options beyond traditional polysaccharide formulations, which in turn affects programmatic recommendations and age-targeted immunization strategies. Concurrently, regulatory authorities are streamlining pathways for immunobridging and accelerated approvals, enabling faster deployment of next-generation candidates in high-need contexts.
Shifts in distribution and procurement are also evident as healthcare systems adopt hybrid pharmacy models and digital ordering platforms that enhance reach while imposing new requirements for traceability and cold-chain integrity. Public-private collaboration models are becoming more common, with manufacturers and health agencies co-designing outbreak response stockpiles and regional manufacturing partnerships to mitigate supply risk. As a result, organizations must reevaluate R&D prioritization, commercial strategies, and stakeholder engagement models to align with an environment that rewards agility, evidence-based policy alignment, and manufacturing resilience.
Assessment of how 2025 tariff changes have reshaped sourcing, manufacturing localization, and procurement risk-sharing across vaccine value chains
The cumulative effects of new tariff measures introduced in 2025 have reverberated across procurement pathways, manufacturing economics, and strategic sourcing decisions for vaccine makers and immunization programs. Tariff adjustments on inputs and finished goods have compelled manufacturers to reexamine global supply footprints and to accelerate initiatives that localize production or secure preferential trade arrangements. At the same time, downstream purchasers and public health purchasers have confronted higher landed costs and longer lead times for certain imported components, prompting a rebalancing toward regional suppliers where capacity permits.
Regulatory and contracting responses have emerged to mitigate tariff-induced disruption, with long-term procurement agreements incorporating price escalation clauses and contingency provisions to preserve continuity of supply. In parallel, the tariff environment has strengthened the business case for investments in domestic fill-and-finish capabilities and for strategic inventory buffers that reduce exposure to cross-border volatility. These adaptations do not eliminate complexity, but they do create clearer incentives for vertically integrated approaches and for collaborative risk-sharing mechanisms between manufacturers, payers, and governments to sustain vaccine availability under shifting trade conditions.
Segment-driven insights that map vaccine type, demographic targeting, formulation choices, distribution pathways, and clinical end-use to strategic decisions
Segmentation analysis reveals differentiated imperatives across vaccine types, age cohorts, formulation approaches, distribution channels, and end-user settings that collectively determine both clinical outcomes and commercial viability. Based on Vaccine Type, market is studied across Conjugate, Polysaccharide, and Protein Subunit, and each category presents distinct immunogenic profiles, storage needs, and lifecycle pathways that influence R&D allocation and regulatory strategies. Based on Age Group, market is studied across Adolescent, Adult, Geriatric, and Pediatric, revealing that immunization schedules and risk-benefit assessments vary sharply by cohort and require targeted communication and delivery models. Based on Formulation, market is studied across Multi Dose and Single Dose, which drives decisions on vial presentation, wastage mitigation, and cold-chain footprint.
Based on Distribution Channel, market is studied across Hospital Pharmacy, Online Pharmacy, and Retail Pharmacy, highlighting the growing role of digital ordering, last-mile dispensing considerations, and patient convenience in routine immunization uptake. Based on End User, market is studied across Clinics, Hospitals, Research Institutes, and Vaccination Centers, which underscores divergent procurement processes, clinical workflows, and post-vaccination surveillance capabilities. Based on Indication, market is studied across Outbreak Response, Routine Prophylactic, and Traveler Immunization, delineating distinct operational timelines, stockpile strategies, and messaging priorities. Taken together, these segmentation lenses inform differentiated commercialization approaches and operational investments that align product attributes with real-world administration settings.
Regional profiles highlighting how distinct regulatory, manufacturing, and delivery ecosystems shape access, preparedness, and partnership opportunities
Regional dynamics introduce important variation in regulatory environments, health financing mechanisms, and delivery infrastructure that influence vaccine access and prioritization. In the Americas, established immunization programs and well-developed commercial channels coexist with pockets of access inequity that require targeted policy interventions and supply chain optimizations. Health systems in this region often balance centralized public procurement with private-sector distribution, necessitating tailored engagement strategies that address diverse payers and service delivery models.
Europe, Middle East & Africa presents a complex mix of high-capacity regulatory authorities alongside countries with fragile health systems where outbreak response readiness is a primary concern; here, regional manufacturing hubs and pooled procurement initiatives play a pivotal role in improving resilience and equitable access. Finally, the Asia-Pacific region exhibits rapid capacity expansion, strong pharmaceutical manufacturing ecosystems, and growing investments in domestic bioprocessing that enable faster scale-up and technology transfer for vaccine production. Taken together, these regional profiles indicate clear opportunities for partnerships that combine manufacturing scale, regulatory harmonization, and programmatic support to close coverage gaps and enhance preparedness.
How incumbent manufacturers and innovative biotech entrants are redefining competition through targeted innovation, partnerships, and capacity investments
Established vaccine manufacturers and dynamic biotechnology entrants are each shaping competitive dynamics through differentiated strategies that emphasize product innovation, strategic collaborations, and capacity expansion. Leading players are concentrating on next-generation conjugate chemistry and protein subunit platforms to extend protection across serogroups and age cohorts, while also optimizing manufacturing throughput and supply agreements to strengthen commercial defensibility. Simultaneously, smaller innovators and academic spinouts are contributing to the pipeline via targeted antigen design and adjuvant research that could enable more effective or broader-spectrum formulations.
Strategic collaborations-including licensing, co-development, and contract manufacturing partnerships-remain central to accelerating access and managing capital intensity. Business models are also evolving to incorporate tiered pricing, risk-sharing agreements with public purchasers, and greater emphasis on post-market evidence generation to support policy adoption. Competitive differentiation increasingly derives from integrated capabilities that combine regulatory agility, localized manufacturing or fill-and-finish capacity, and robust pharmacovigilance systems that satisfy payer and regulator requirements while reinforcing public trust.
Concrete strategic actions for manufacturers and stakeholders to enhance supply resilience, accelerate approvals, and align commercial models with public health priorities
Industry leaders should implement a set of actionable measures to strengthen resilience, accelerate access, and sustain commercial performance in a rapidly changing environment. First, diversify manufacturing and supply chains by investing in regional fill-and-finish capabilities, and by establishing multi-sourcing arrangements for critical inputs to reduce exposure to trade shocks and tariff volatility. Second, prioritize R&D that advances conjugate and protein subunit platforms while optimizing formulations for single-dose or multidose presentations that best match programmatic needs and minimize wastage. Third, deepen engagement with regulators to pursue adaptive pathways, immunobridging studies, and evidence packages that shorten approval timelines and improve alignment with public health priorities.
Additionally, enhance distribution agility through digital inventory management and partnerships with hospital and retail pharmacy channels to improve uptake and traceability. Strengthen commercial models with flexible contracting, value-based arrangements, and targeted pricing strategies that reflect regional purchasing power and programmatic objectives. Finally, build robust post-market surveillance and communication strategies that reinforce vaccine confidence, support real-world effectiveness evaluations, and provide the data needed for broad policy adoption and sustained uptake.
A rigorous mixed-methods approach combining expert interviews, literature synthesis, and scenario analysis to validate strategic insights and operational implications
This research integrates primary and secondary methodologies to ensure analytic rigor, transparency, and actionable insight generation. Primary research included structured interviews with clinical experts, supply chain leaders, regulatory officials, and procurement specialists to capture frontline perspectives on operational constraints and strategic priorities. Secondary research encompassed a systematic review of peer-reviewed literature, regulatory guidance documents, public health agency recommendations, and company disclosures to construct an evidence base for technology trends, product attributes, and programmatic approaches.
Data were triangulated across sources to validate findings and to reconcile divergent perspectives. Scenario analysis was applied to stress-test supply chain assumptions and to evaluate the operational implications of tariff and policy shifts. Quality controls included cross-validation of interview transcripts, independent review by subject-matter experts, and documentation of assumptions and limitations. Ethical considerations guided stakeholder engagement, with interview respondents anonymized where requested and proprietary information treated under strict confidentiality protocols. Collectively, these methods produced a robust, reproducible framework for evaluating strategic choices across development, manufacturing, and distribution domains.
A decisive synthesis highlighting strategic crossroads and practical pathways to strengthen access, readiness, and innovation across the meningococcal vaccine ecosystem
In conclusion, the meningococcal vaccine ecosystem is at an inflection point where scientific advances, evolving distribution models, and shifting trade policy combine to redefine strategic priorities for stakeholders. Conjugate and protein subunit innovations expand clinical options while presenting new operational requirements for formulation selection and cold-chain management. Distribution modernization and digital channel expansion create routes to improved coverage but necessitate investments in traceability and last-mile logistics. Tariff-driven shifts and the imperative for supply resilience underscore the importance of manufacturing localization and risk-sharing contracts that protect continuity of supply.
Decision-makers should therefore balance near-term operational needs with medium-term investments in platform innovation and manufacturing capacity. Collaboration between manufacturers, health authorities, and service providers will be critical to aligning incentives, accelerating access, and maintaining public confidence. The combined focus on adaptive regulation, targeted segmentation strategies, and regional partnerships offers a pragmatic pathway to enhance preparedness and equitable access to meningococcal vaccines across diverse health systems.
Please Note: PDF & Excel + Online Access - 1 Year
A concise framing of the contemporary meningococcal vaccine landscape connecting immunology advances with deployment, policy drivers, and operational priorities
Meningococcal disease remains a persistent public health challenge due to its rapid onset and potentially severe outcomes, and stakeholders require a clear, operationally focused synthesis of current vaccine modalities, delivery systems, and policy drivers. This executive summary synthesizes recent advances in conjugate and protein subunit immunology, evolving immunization schedules across age cohorts, and the logistical imperatives that now shape procurement decisions. It further contextualizes how distribution channels, clinical end users, and indication-specific requirements converge to inform deployment strategies in routine and emergency settings.
The introduction frames the landscape by connecting scientific progress with real-world programmatic constraints. It highlights how vaccine formulation choices influence cold-chain logistics, dose-sparing strategies, and post-marketing surveillance, while also noting that demographic targeting-spanning pediatric immunization programs through geriatric and traveler cohorts-affects uptake and resource allocation. Finally, the introduction outlines the principal analytic lenses used throughout the report, emphasizing readiness for outbreak response, resilience of supply chains, and the strategic interplay between public health objectives and commercial imperatives.
How scientific, regulatory, and distribution innovations are reshaping product development, procurement strategies, and outbreak preparedness across the sector
The meningococcal vaccine landscape is undergoing transformative shifts driven by scientific innovation, regulatory evolution, and new delivery paradigms that together change how stakeholders plan and invest. Advances in protein subunit vaccines and improvements to conjugate chemistry are expanding protective options beyond traditional polysaccharide formulations, which in turn affects programmatic recommendations and age-targeted immunization strategies. Concurrently, regulatory authorities are streamlining pathways for immunobridging and accelerated approvals, enabling faster deployment of next-generation candidates in high-need contexts.
Shifts in distribution and procurement are also evident as healthcare systems adopt hybrid pharmacy models and digital ordering platforms that enhance reach while imposing new requirements for traceability and cold-chain integrity. Public-private collaboration models are becoming more common, with manufacturers and health agencies co-designing outbreak response stockpiles and regional manufacturing partnerships to mitigate supply risk. As a result, organizations must reevaluate R&D prioritization, commercial strategies, and stakeholder engagement models to align with an environment that rewards agility, evidence-based policy alignment, and manufacturing resilience.
Assessment of how 2025 tariff changes have reshaped sourcing, manufacturing localization, and procurement risk-sharing across vaccine value chains
The cumulative effects of new tariff measures introduced in 2025 have reverberated across procurement pathways, manufacturing economics, and strategic sourcing decisions for vaccine makers and immunization programs. Tariff adjustments on inputs and finished goods have compelled manufacturers to reexamine global supply footprints and to accelerate initiatives that localize production or secure preferential trade arrangements. At the same time, downstream purchasers and public health purchasers have confronted higher landed costs and longer lead times for certain imported components, prompting a rebalancing toward regional suppliers where capacity permits.
Regulatory and contracting responses have emerged to mitigate tariff-induced disruption, with long-term procurement agreements incorporating price escalation clauses and contingency provisions to preserve continuity of supply. In parallel, the tariff environment has strengthened the business case for investments in domestic fill-and-finish capabilities and for strategic inventory buffers that reduce exposure to cross-border volatility. These adaptations do not eliminate complexity, but they do create clearer incentives for vertically integrated approaches and for collaborative risk-sharing mechanisms between manufacturers, payers, and governments to sustain vaccine availability under shifting trade conditions.
Segment-driven insights that map vaccine type, demographic targeting, formulation choices, distribution pathways, and clinical end-use to strategic decisions
Segmentation analysis reveals differentiated imperatives across vaccine types, age cohorts, formulation approaches, distribution channels, and end-user settings that collectively determine both clinical outcomes and commercial viability. Based on Vaccine Type, market is studied across Conjugate, Polysaccharide, and Protein Subunit, and each category presents distinct immunogenic profiles, storage needs, and lifecycle pathways that influence R&D allocation and regulatory strategies. Based on Age Group, market is studied across Adolescent, Adult, Geriatric, and Pediatric, revealing that immunization schedules and risk-benefit assessments vary sharply by cohort and require targeted communication and delivery models. Based on Formulation, market is studied across Multi Dose and Single Dose, which drives decisions on vial presentation, wastage mitigation, and cold-chain footprint.
Based on Distribution Channel, market is studied across Hospital Pharmacy, Online Pharmacy, and Retail Pharmacy, highlighting the growing role of digital ordering, last-mile dispensing considerations, and patient convenience in routine immunization uptake. Based on End User, market is studied across Clinics, Hospitals, Research Institutes, and Vaccination Centers, which underscores divergent procurement processes, clinical workflows, and post-vaccination surveillance capabilities. Based on Indication, market is studied across Outbreak Response, Routine Prophylactic, and Traveler Immunization, delineating distinct operational timelines, stockpile strategies, and messaging priorities. Taken together, these segmentation lenses inform differentiated commercialization approaches and operational investments that align product attributes with real-world administration settings.
Regional profiles highlighting how distinct regulatory, manufacturing, and delivery ecosystems shape access, preparedness, and partnership opportunities
Regional dynamics introduce important variation in regulatory environments, health financing mechanisms, and delivery infrastructure that influence vaccine access and prioritization. In the Americas, established immunization programs and well-developed commercial channels coexist with pockets of access inequity that require targeted policy interventions and supply chain optimizations. Health systems in this region often balance centralized public procurement with private-sector distribution, necessitating tailored engagement strategies that address diverse payers and service delivery models.
Europe, Middle East & Africa presents a complex mix of high-capacity regulatory authorities alongside countries with fragile health systems where outbreak response readiness is a primary concern; here, regional manufacturing hubs and pooled procurement initiatives play a pivotal role in improving resilience and equitable access. Finally, the Asia-Pacific region exhibits rapid capacity expansion, strong pharmaceutical manufacturing ecosystems, and growing investments in domestic bioprocessing that enable faster scale-up and technology transfer for vaccine production. Taken together, these regional profiles indicate clear opportunities for partnerships that combine manufacturing scale, regulatory harmonization, and programmatic support to close coverage gaps and enhance preparedness.
How incumbent manufacturers and innovative biotech entrants are redefining competition through targeted innovation, partnerships, and capacity investments
Established vaccine manufacturers and dynamic biotechnology entrants are each shaping competitive dynamics through differentiated strategies that emphasize product innovation, strategic collaborations, and capacity expansion. Leading players are concentrating on next-generation conjugate chemistry and protein subunit platforms to extend protection across serogroups and age cohorts, while also optimizing manufacturing throughput and supply agreements to strengthen commercial defensibility. Simultaneously, smaller innovators and academic spinouts are contributing to the pipeline via targeted antigen design and adjuvant research that could enable more effective or broader-spectrum formulations.
Strategic collaborations-including licensing, co-development, and contract manufacturing partnerships-remain central to accelerating access and managing capital intensity. Business models are also evolving to incorporate tiered pricing, risk-sharing agreements with public purchasers, and greater emphasis on post-market evidence generation to support policy adoption. Competitive differentiation increasingly derives from integrated capabilities that combine regulatory agility, localized manufacturing or fill-and-finish capacity, and robust pharmacovigilance systems that satisfy payer and regulator requirements while reinforcing public trust.
Concrete strategic actions for manufacturers and stakeholders to enhance supply resilience, accelerate approvals, and align commercial models with public health priorities
Industry leaders should implement a set of actionable measures to strengthen resilience, accelerate access, and sustain commercial performance in a rapidly changing environment. First, diversify manufacturing and supply chains by investing in regional fill-and-finish capabilities, and by establishing multi-sourcing arrangements for critical inputs to reduce exposure to trade shocks and tariff volatility. Second, prioritize R&D that advances conjugate and protein subunit platforms while optimizing formulations for single-dose or multidose presentations that best match programmatic needs and minimize wastage. Third, deepen engagement with regulators to pursue adaptive pathways, immunobridging studies, and evidence packages that shorten approval timelines and improve alignment with public health priorities.
Additionally, enhance distribution agility through digital inventory management and partnerships with hospital and retail pharmacy channels to improve uptake and traceability. Strengthen commercial models with flexible contracting, value-based arrangements, and targeted pricing strategies that reflect regional purchasing power and programmatic objectives. Finally, build robust post-market surveillance and communication strategies that reinforce vaccine confidence, support real-world effectiveness evaluations, and provide the data needed for broad policy adoption and sustained uptake.
A rigorous mixed-methods approach combining expert interviews, literature synthesis, and scenario analysis to validate strategic insights and operational implications
This research integrates primary and secondary methodologies to ensure analytic rigor, transparency, and actionable insight generation. Primary research included structured interviews with clinical experts, supply chain leaders, regulatory officials, and procurement specialists to capture frontline perspectives on operational constraints and strategic priorities. Secondary research encompassed a systematic review of peer-reviewed literature, regulatory guidance documents, public health agency recommendations, and company disclosures to construct an evidence base for technology trends, product attributes, and programmatic approaches.
Data were triangulated across sources to validate findings and to reconcile divergent perspectives. Scenario analysis was applied to stress-test supply chain assumptions and to evaluate the operational implications of tariff and policy shifts. Quality controls included cross-validation of interview transcripts, independent review by subject-matter experts, and documentation of assumptions and limitations. Ethical considerations guided stakeholder engagement, with interview respondents anonymized where requested and proprietary information treated under strict confidentiality protocols. Collectively, these methods produced a robust, reproducible framework for evaluating strategic choices across development, manufacturing, and distribution domains.
A decisive synthesis highlighting strategic crossroads and practical pathways to strengthen access, readiness, and innovation across the meningococcal vaccine ecosystem
In conclusion, the meningococcal vaccine ecosystem is at an inflection point where scientific advances, evolving distribution models, and shifting trade policy combine to redefine strategic priorities for stakeholders. Conjugate and protein subunit innovations expand clinical options while presenting new operational requirements for formulation selection and cold-chain management. Distribution modernization and digital channel expansion create routes to improved coverage but necessitate investments in traceability and last-mile logistics. Tariff-driven shifts and the imperative for supply resilience underscore the importance of manufacturing localization and risk-sharing contracts that protect continuity of supply.
Decision-makers should therefore balance near-term operational needs with medium-term investments in platform innovation and manufacturing capacity. Collaboration between manufacturers, health authorities, and service providers will be critical to aligning incentives, accelerating access, and maintaining public confidence. The combined focus on adaptive regulation, targeted segmentation strategies, and regional partnerships offers a pragmatic pathway to enhance preparedness and equitable access to meningococcal vaccines across diverse health systems.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
199 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Expansion of multivalent meningococcal B vaccines into adolescent immunization programs across Europe due to rising serogroup prevalence
- 5.2. Integration of meningococcal quadrivalent conjugate vaccines with routine adolescent and college-entry immunization schedules in North America
- 5.3. Strategic partnerships between vaccine manufacturers and public health agencies to enhance outbreak response capabilities in sub-Saharan Africa
- 5.4. Development of combination vaccines targeting meningococcal ACWY and other pediatric pathogens to streamline immunization schedules for infants and toddlers
- 5.5. Emergence of vaccine hesitancy impacting meningococcal immunization coverage rates among young adults in high-income countries
- 5.6. Adoption of novel conjugation technologies to improve immunogenicity and reduce reactogenicity in next-generation meningococcal vaccines
- 5.7. Impact of dynamic serogroup replacement patterns on regional vaccine formulation and procurement strategies across global markets
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Meningococcal Vaccines Market, by Vaccine Type
- 8.1. Conjugate
- 8.2. Polysaccharide
- 8.3. Protein Subunit
- 9. Meningococcal Vaccines Market, by Age Group
- 9.1. Adolescent
- 9.2. Adult
- 9.3. Geriatric
- 9.4. Pediatric
- 10. Meningococcal Vaccines Market, by Formulation
- 10.1. Multi Dose
- 10.2. Single Dose
- 11. Meningococcal Vaccines Market, by Distribution Channel
- 11.1. Hospital Pharmacy
- 11.2. Online Pharmacy
- 11.3. Retail Pharmacy
- 12. Meningococcal Vaccines Market, by End User
- 12.1. Clinics
- 12.2. Hospitals
- 12.3. Research Institutes
- 12.4. Vaccination Centers
- 13. Meningococcal Vaccines Market, by Indication
- 13.1. Outbreak Response
- 13.2. Routine Prophylactic
- 13.3. Traveler Immunization
- 14. Meningococcal Vaccines 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. Meningococcal Vaccines Market, by Group
- 15.1. ASEAN
- 15.2. GCC
- 15.3. European Union
- 15.4. BRICS
- 15.5. G7
- 15.6. NATO
- 16. Meningococcal Vaccines 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. Competitive Landscape
- 17.1. Market Share Analysis, 2024
- 17.2. FPNV Positioning Matrix, 2024
- 17.3. Competitive Analysis
- 17.3.1. Astellas Pharma Inc.
- 17.3.2. AstraZeneca PLC
- 17.3.3. Bharat Biotech Ltd.
- 17.3.4. GlaxoSmithKline PLC
- 17.3.5. Incepta Pharmaceuticals Ltd.
- 17.3.6. Merck & Co., Inc.
- 17.3.7. Novartis AG
- 17.3.8. Pfizer Inc.
- 17.3.9. Sanofi S.A.
- 17.3.10. Serum Institute of India Pvt. Ltd.
- 17.3.11. Taj Pharmaceuticals Limited
- 17.3.12. PT Bio Farma
- 17.3.13. Bio-Med Private Ltd
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