Syringes Market by Type (Disposable, Reusable), Material (Glass, Plastic, Stainless Steel), Technology, Volume, End User - Global Forecast 2025-2032
Description
The Syringes Market was valued at USD 13.24 billion in 2024 and is projected to grow to USD 14.05 billion in 2025, with a CAGR of 7.75%, reaching USD 24.06 billion by 2032.
Comprehensive introduction outlining syringe market fundamentals, clinical drivers, manufacturing complexities, supply chain resilience, and stakeholder needs
This introduction establishes a clear foundation for understanding the contemporary syringe landscape, synthesizing clinical demand drivers, manufacturing intricacies, regulatory expectations, and evolving procurement priorities. It begins by framing the clinical context: increased emphasis on outpatient care, immunization programs, and injectable biologics has elevated the operational importance of syringe design, safety, and compatibility with delivery systems. At the same time, manufacturers confront complex production constraints that include raw material selection, sterilization pathways, and quality control protocols that directly influence product reliability and lifecycle costs.
From a regulatory perspective, agencies globally are tightening device safety requirements and post-market surveillance obligations, which is prompting firms to invest in traceability and enhanced safety features. Transitioning from volume-focused procurement to value-informed purchasing has shifted stakeholder attention toward device usability, infection prevention, and integrated solutions that reduce clinician error. As a result, procurement teams and product leaders must balance short-term supply resiliency with longer-term investments in design architecture, manufacturing automation, and supplier diversification. Throughout this introduction, the emphasis remains on practical implications for decision-makers, highlighting where attention and resources will most effectively reduce risk and unlock clinical and commercial value.
Mapping transformative shifts reshaping syringe development and adoption: digital health integration, advanced materials, safety and decentralized care models
The current landscape is undergoing several transformative shifts that are redefining how syringes are developed, regulated, and consumed. First, technological integration is accelerating; digital and connected features that enable dose confirmation, tracking, and compatibility with electronic health records are moving from experimental to commercially viable. These advances affect not only product design but also the ecosystem of service providers, reimbursement models, and clinical workflows. Next, materials innovation is influencing performance attributes: novel polymers and refined glass formulations are enabling thinner walls, improved clarity, and enhanced chemical compatibility for biologics and small-molecule injectables.
Concurrently, safety and sustainability imperatives are reshaping procurement criteria. Safety mechanisms designed to reduce needlestick injuries are being prioritized alongside lifecycle assessments that consider disposability, reuse potential, and recyclability. Decentralized care models, including home administration and community clinics, are driving demand for user-friendly devices and prefilled delivery formats. Finally, clinical and regulatory communities are converging on harmonized standards for device performance and post-market data collection, prompting manufacturers to embed quality-by-design principles and real-world evidence strategies into development roadmaps. Together, these shifts create new strategic imperatives for product differentiation, supply chain agility, and cross-functional collaboration.
Evaluating cumulative economic, supply chain, and innovation impacts of the United States tariffs announced in 2025 on syringe manufacturing and distribution
The tariffs enacted by the United States in 2025 introduced multi-dimensional effects across cost structures, sourcing decisions, and strategic planning for syringe manufacturers and buyers. Immediately, procurement teams faced changes in landed costs for imported components and finished devices, which prompted many organizations to reassess supplier contracts and re-evaluate nearshoring options. Over time, firms that relied on single-source imports experienced pressure to diversify supplier bases, invest in dual-sourcing, or accelerate transfer of production closer to end markets to mitigate tariff exposure. These tactical responses often required capital allocation for additional supplier qualification, regulatory filings, and localized quality assurance.
In parallel, the tariffs incentivized a subset of manufacturers to invest in automation and process efficiency to offset increased input costs. R&D priorities shifted subtly as firms prioritized component designs that relied less on tariff-affected subcomponents, and purchasing teams adopted more rigorous total-cost-of-ownership frameworks. The policy also catalyzed dialogue between industry and regulators on trade policy alignment and critical medical device exemptions, leading some stakeholders to pursue tariff relief or phased implementation. Overall, the 2025 tariff measures acted as a catalyst for supply chain reconfiguration, risk mitigation initiatives, and a renewed focus on domestic manufacturing resilience.
Actionable segmentation insights integrating product type, material composition, technology variants, and volumetric classifications to guide product strategy and resource allocation
Segmentation analysis reveals differentiated opportunities and operational challenges across product types, materials, technologies, and production volumes, each of which informs distinct strategic choices for manufacturers and procurement teams. Based on Type, market is studied across Disposable and Reusable, and this dichotomy drives decisions about sterilization methods, lifecycle costs, and end-user training. Disposable designs emphasize single-use safety and simplicity, while reusable systems demand validated reprocessing protocols and durable materials. Based on Material, market is studied across Glass, Plastic, and Stainless Steel; glass remains critical for chemical compatibility with certain biologics, plastics enable lightweight and cost-effective disposability, and stainless steel is preferred where durability and sterilizability are paramount.
Based on Technology, market is studied across Prefill, Safety, Smart, and Standard. The Prefill is further studied across Auto Injector and Cartridge, reflecting distinctions in user interface and integration with drug delivery platforms. The Safety is further studied across Active and Passive, which differentiates mechanisms that require user action from those that deploy automatically to prevent needlestick events. Smart systems incorporate sensors and connectivity to support adherence and traceability, while Standard technologies prioritize cost and broad compatibility. Based on Volume, market is studied across High Volume, Low Volume, and Medium Volume; production scale influences capital investment choices, quality control throughput, and supplier negotiation leverage. These segmentation lenses together guide targeted product development, regulatory strategy, and commercialization tactics tailored to user needs and manufacturing capabilities.
Regional intelligence on demand drivers, manufacturing strengths, regulatory divergence, and logistics across Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape product design priorities, regulatory strategy, and supply chain architecture, with distinct levers active in each major geography. In the Americas, demand patterns are influenced by large immunization programs, advanced healthcare infrastructure, and a preference for devices that support outpatient and community-based delivery. Supply chain resilience is a focus, prompting investments in domestic manufacturing capabilities and supplier partnerships that shorten lead times.
In Europe, Middle East & Africa, regulatory diversity and fragmented procurement systems require flexible regulatory strategies and adaptable commercial models. European markets emphasize safety features and environmental considerations, whereas markets across the Middle East and Africa present heterogeneous demand profiles that call for a range of product cost points and distribution approaches. Transitioning to Asia-Pacific, the region combines significant manufacturing capacity with diverse clinical settings; opportunities arise from both large-scale production ecosystems and rapidly evolving point-of-care delivery models. Across all regions, cross-border logistics and regulatory harmonization remain critical factors, and stakeholders must tailor market entry and scale-up strategies to local reimbursement regimes, clinical practice patterns, and supplier ecosystems.
Strategic company-level insights highlighting competitive positioning, innovation portfolios, mergers and partnerships, and supply chain adaptations
Company-level analysis highlights how industry leaders and challenger firms are positioning around technology investment, capacity expansion, and strategic partnerships. Leading manufacturers are prioritizing portfolios that combine safety-enabled disposables, prefilled systems for biologics, and smart devices that enhance traceability and adherence. These firms are also allocating resources to manufacturing automation and quality systems to accelerate time-to-market while maintaining regulatory compliance. Mid-sized and niche players are differentiating through specialized material expertise, bespoke delivery formats, and targeted clinical segments where close collaboration with pharmaceutical partners yields higher value.
Partnerships and alliances are increasingly central to competitive advantage. Examples include co-development agreements between device makers and drug developers to deliver integrated combination products, and supply agreements that secure critical components. Mergers and acquisitions remain an avenue for rapid capability expansion, especially where acquiring sterilization capacity or injection-mold expertise can shorten commercialization timelines. Across the competitive landscape, companies that combine technical excellence with agile supply chain strategies are best positioned to meet evolving customer expectations and regulatory demands.
Targeted recommendations for manufacturers, healthcare providers, and policymakers to accelerate safe, cost-effective syringe deployment while fostering innovation
Industry leaders should adopt a set of practical, prioritized actions to protect margins, accelerate innovation, and improve patient safety. First, firms must embed design-for-manufacturing principles early in product development to minimize downstream quality issues and support scalable automation. Investing in modular production lines and flexible tooling will enable rapid response to demand shifts and tariff-induced sourcing variability. Second, organizations should intensify collaboration with clinical stakeholders to validate safety features and user ergonomics, ensuring that innovations translate into measurable reductions in administration errors and needlestick incidents.
Third, stakeholders need to diversify supplier bases and qualify secondary sources for critical components, supported by robust supplier risk assessment frameworks. Fourth, payers and procurement teams should evolve purchasing criteria to incorporate total-cost-of-ownership and clinical outcome metrics, which will reward higher-value devices and drive uptake of prefilled and safety-enabled formats. Finally, companies should pursue targeted digital initiatives-such as basic connectivity for adherence verification and supply chain traceability-that add clear clinical or operational value while remaining cost-effective. Together, these recommendations create a pragmatic roadmap to enhance resilience, reduce clinical risk, and capture differentiated value across care settings.
Transparent research methodology describing data collection, expert interviews, validation protocols, and quantitative and qualitative techniques to ensure rigor
The research methodology combines primary qualitative engagement with subject-matter experts, rigorous secondary research, and structured data validation to produce credible insights. Primary inputs include interviews with clinical leaders, procurement specialists, regulatory consultants, and manufacturing technologists, which provide context on real-world device performance, adoption barriers, and procurement priorities. Secondary research encompasses public regulatory guidance, technical standards, patent literature, and credible industry analyses that inform technical assessments and trend identification.
Quantitative techniques include synthesis of production and trade data, along with scenario analysis to evaluate supply chain vulnerabilities and cost drivers. Validation protocols incorporate triangulation across independent sources, cross-referencing interview insights with documented standards, and peer review by external experts in device manufacturing and clinical administration. Throughout the process, emphasis is placed on transparency of assumptions, traceability of data sources, and clear documentation of methodological limitations to support confident interpretation of findings and to enable replication of analytic steps where required.
Concise conclusion synthesizing strategic takeaways, risk considerations, and forward-looking priorities to inform decision-making for industry decision-makers
In conclusion, the syringe landscape is at a strategic inflection point driven by technological convergence, regulatory tightening, and shifting care delivery paradigms. The interplay between materials science, safety engineering, and digital augmentation is creating opportunities for product differentiation that deliver measurable clinical and operational benefits. Simultaneously, policy changes and trade measures have accelerated supply chain reconfiguration and renewed emphasis on production resilience. Decision-makers must therefore balance near-term continuity measures with longer-term investments in design, automation, and strategic partnerships.
Looking forward, success will favor organizations that align product development with real-world clinical needs, adopt flexible manufacturing approaches, and proactively engage with regulators and payers to demonstrate device value. By synthesizing the strategic takeaways, cautionary themes, and priority actions presented in this summary, leaders can better navigate uncertainty, reduce patient risk, and capture opportunities for sustainable innovation. The insights provided here are intended to inform pragmatic decision-making and to guide focused investments that deliver both clinical impact and commercial returns.
Please Note: PDF & Excel + Online Access - 1 Year
Comprehensive introduction outlining syringe market fundamentals, clinical drivers, manufacturing complexities, supply chain resilience, and stakeholder needs
This introduction establishes a clear foundation for understanding the contemporary syringe landscape, synthesizing clinical demand drivers, manufacturing intricacies, regulatory expectations, and evolving procurement priorities. It begins by framing the clinical context: increased emphasis on outpatient care, immunization programs, and injectable biologics has elevated the operational importance of syringe design, safety, and compatibility with delivery systems. At the same time, manufacturers confront complex production constraints that include raw material selection, sterilization pathways, and quality control protocols that directly influence product reliability and lifecycle costs.
From a regulatory perspective, agencies globally are tightening device safety requirements and post-market surveillance obligations, which is prompting firms to invest in traceability and enhanced safety features. Transitioning from volume-focused procurement to value-informed purchasing has shifted stakeholder attention toward device usability, infection prevention, and integrated solutions that reduce clinician error. As a result, procurement teams and product leaders must balance short-term supply resiliency with longer-term investments in design architecture, manufacturing automation, and supplier diversification. Throughout this introduction, the emphasis remains on practical implications for decision-makers, highlighting where attention and resources will most effectively reduce risk and unlock clinical and commercial value.
Mapping transformative shifts reshaping syringe development and adoption: digital health integration, advanced materials, safety and decentralized care models
The current landscape is undergoing several transformative shifts that are redefining how syringes are developed, regulated, and consumed. First, technological integration is accelerating; digital and connected features that enable dose confirmation, tracking, and compatibility with electronic health records are moving from experimental to commercially viable. These advances affect not only product design but also the ecosystem of service providers, reimbursement models, and clinical workflows. Next, materials innovation is influencing performance attributes: novel polymers and refined glass formulations are enabling thinner walls, improved clarity, and enhanced chemical compatibility for biologics and small-molecule injectables.
Concurrently, safety and sustainability imperatives are reshaping procurement criteria. Safety mechanisms designed to reduce needlestick injuries are being prioritized alongside lifecycle assessments that consider disposability, reuse potential, and recyclability. Decentralized care models, including home administration and community clinics, are driving demand for user-friendly devices and prefilled delivery formats. Finally, clinical and regulatory communities are converging on harmonized standards for device performance and post-market data collection, prompting manufacturers to embed quality-by-design principles and real-world evidence strategies into development roadmaps. Together, these shifts create new strategic imperatives for product differentiation, supply chain agility, and cross-functional collaboration.
Evaluating cumulative economic, supply chain, and innovation impacts of the United States tariffs announced in 2025 on syringe manufacturing and distribution
The tariffs enacted by the United States in 2025 introduced multi-dimensional effects across cost structures, sourcing decisions, and strategic planning for syringe manufacturers and buyers. Immediately, procurement teams faced changes in landed costs for imported components and finished devices, which prompted many organizations to reassess supplier contracts and re-evaluate nearshoring options. Over time, firms that relied on single-source imports experienced pressure to diversify supplier bases, invest in dual-sourcing, or accelerate transfer of production closer to end markets to mitigate tariff exposure. These tactical responses often required capital allocation for additional supplier qualification, regulatory filings, and localized quality assurance.
In parallel, the tariffs incentivized a subset of manufacturers to invest in automation and process efficiency to offset increased input costs. R&D priorities shifted subtly as firms prioritized component designs that relied less on tariff-affected subcomponents, and purchasing teams adopted more rigorous total-cost-of-ownership frameworks. The policy also catalyzed dialogue between industry and regulators on trade policy alignment and critical medical device exemptions, leading some stakeholders to pursue tariff relief or phased implementation. Overall, the 2025 tariff measures acted as a catalyst for supply chain reconfiguration, risk mitigation initiatives, and a renewed focus on domestic manufacturing resilience.
Actionable segmentation insights integrating product type, material composition, technology variants, and volumetric classifications to guide product strategy and resource allocation
Segmentation analysis reveals differentiated opportunities and operational challenges across product types, materials, technologies, and production volumes, each of which informs distinct strategic choices for manufacturers and procurement teams. Based on Type, market is studied across Disposable and Reusable, and this dichotomy drives decisions about sterilization methods, lifecycle costs, and end-user training. Disposable designs emphasize single-use safety and simplicity, while reusable systems demand validated reprocessing protocols and durable materials. Based on Material, market is studied across Glass, Plastic, and Stainless Steel; glass remains critical for chemical compatibility with certain biologics, plastics enable lightweight and cost-effective disposability, and stainless steel is preferred where durability and sterilizability are paramount.
Based on Technology, market is studied across Prefill, Safety, Smart, and Standard. The Prefill is further studied across Auto Injector and Cartridge, reflecting distinctions in user interface and integration with drug delivery platforms. The Safety is further studied across Active and Passive, which differentiates mechanisms that require user action from those that deploy automatically to prevent needlestick events. Smart systems incorporate sensors and connectivity to support adherence and traceability, while Standard technologies prioritize cost and broad compatibility. Based on Volume, market is studied across High Volume, Low Volume, and Medium Volume; production scale influences capital investment choices, quality control throughput, and supplier negotiation leverage. These segmentation lenses together guide targeted product development, regulatory strategy, and commercialization tactics tailored to user needs and manufacturing capabilities.
Regional intelligence on demand drivers, manufacturing strengths, regulatory divergence, and logistics across Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape product design priorities, regulatory strategy, and supply chain architecture, with distinct levers active in each major geography. In the Americas, demand patterns are influenced by large immunization programs, advanced healthcare infrastructure, and a preference for devices that support outpatient and community-based delivery. Supply chain resilience is a focus, prompting investments in domestic manufacturing capabilities and supplier partnerships that shorten lead times.
In Europe, Middle East & Africa, regulatory diversity and fragmented procurement systems require flexible regulatory strategies and adaptable commercial models. European markets emphasize safety features and environmental considerations, whereas markets across the Middle East and Africa present heterogeneous demand profiles that call for a range of product cost points and distribution approaches. Transitioning to Asia-Pacific, the region combines significant manufacturing capacity with diverse clinical settings; opportunities arise from both large-scale production ecosystems and rapidly evolving point-of-care delivery models. Across all regions, cross-border logistics and regulatory harmonization remain critical factors, and stakeholders must tailor market entry and scale-up strategies to local reimbursement regimes, clinical practice patterns, and supplier ecosystems.
Strategic company-level insights highlighting competitive positioning, innovation portfolios, mergers and partnerships, and supply chain adaptations
Company-level analysis highlights how industry leaders and challenger firms are positioning around technology investment, capacity expansion, and strategic partnerships. Leading manufacturers are prioritizing portfolios that combine safety-enabled disposables, prefilled systems for biologics, and smart devices that enhance traceability and adherence. These firms are also allocating resources to manufacturing automation and quality systems to accelerate time-to-market while maintaining regulatory compliance. Mid-sized and niche players are differentiating through specialized material expertise, bespoke delivery formats, and targeted clinical segments where close collaboration with pharmaceutical partners yields higher value.
Partnerships and alliances are increasingly central to competitive advantage. Examples include co-development agreements between device makers and drug developers to deliver integrated combination products, and supply agreements that secure critical components. Mergers and acquisitions remain an avenue for rapid capability expansion, especially where acquiring sterilization capacity or injection-mold expertise can shorten commercialization timelines. Across the competitive landscape, companies that combine technical excellence with agile supply chain strategies are best positioned to meet evolving customer expectations and regulatory demands.
Targeted recommendations for manufacturers, healthcare providers, and policymakers to accelerate safe, cost-effective syringe deployment while fostering innovation
Industry leaders should adopt a set of practical, prioritized actions to protect margins, accelerate innovation, and improve patient safety. First, firms must embed design-for-manufacturing principles early in product development to minimize downstream quality issues and support scalable automation. Investing in modular production lines and flexible tooling will enable rapid response to demand shifts and tariff-induced sourcing variability. Second, organizations should intensify collaboration with clinical stakeholders to validate safety features and user ergonomics, ensuring that innovations translate into measurable reductions in administration errors and needlestick incidents.
Third, stakeholders need to diversify supplier bases and qualify secondary sources for critical components, supported by robust supplier risk assessment frameworks. Fourth, payers and procurement teams should evolve purchasing criteria to incorporate total-cost-of-ownership and clinical outcome metrics, which will reward higher-value devices and drive uptake of prefilled and safety-enabled formats. Finally, companies should pursue targeted digital initiatives-such as basic connectivity for adherence verification and supply chain traceability-that add clear clinical or operational value while remaining cost-effective. Together, these recommendations create a pragmatic roadmap to enhance resilience, reduce clinical risk, and capture differentiated value across care settings.
Transparent research methodology describing data collection, expert interviews, validation protocols, and quantitative and qualitative techniques to ensure rigor
The research methodology combines primary qualitative engagement with subject-matter experts, rigorous secondary research, and structured data validation to produce credible insights. Primary inputs include interviews with clinical leaders, procurement specialists, regulatory consultants, and manufacturing technologists, which provide context on real-world device performance, adoption barriers, and procurement priorities. Secondary research encompasses public regulatory guidance, technical standards, patent literature, and credible industry analyses that inform technical assessments and trend identification.
Quantitative techniques include synthesis of production and trade data, along with scenario analysis to evaluate supply chain vulnerabilities and cost drivers. Validation protocols incorporate triangulation across independent sources, cross-referencing interview insights with documented standards, and peer review by external experts in device manufacturing and clinical administration. Throughout the process, emphasis is placed on transparency of assumptions, traceability of data sources, and clear documentation of methodological limitations to support confident interpretation of findings and to enable replication of analytic steps where required.
Concise conclusion synthesizing strategic takeaways, risk considerations, and forward-looking priorities to inform decision-making for industry decision-makers
In conclusion, the syringe landscape is at a strategic inflection point driven by technological convergence, regulatory tightening, and shifting care delivery paradigms. The interplay between materials science, safety engineering, and digital augmentation is creating opportunities for product differentiation that deliver measurable clinical and operational benefits. Simultaneously, policy changes and trade measures have accelerated supply chain reconfiguration and renewed emphasis on production resilience. Decision-makers must therefore balance near-term continuity measures with longer-term investments in design, automation, and strategic partnerships.
Looking forward, success will favor organizations that align product development with real-world clinical needs, adopt flexible manufacturing approaches, and proactively engage with regulators and payers to demonstrate device value. By synthesizing the strategic takeaways, cautionary themes, and priority actions presented in this summary, leaders can better navigate uncertainty, reduce patient risk, and capture opportunities for sustainable innovation. The insights provided here are intended to inform pragmatic decision-making and to guide focused investments that deliver both clinical impact and commercial returns.
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. Growing adoption of safety-engineered auto-disable syringes to prevent needlestick injuries in healthcare settings
- 5.2. Increasing demand for prefilled glass syringes in biologic drug administration and vaccine delivery
- 5.3. Rising regulatory mandates for single-use auto-disable syringes in low-income countries to curb disease transmission
- 5.4. Emergence of smart syringes with IoT-enabled dose tracking and usage monitoring for improved patient compliance
- 5.5. Shift towards eco-friendly biodegradable plastics and latex-free materials in disposable syringe manufacturing
- 5.6. Expanding investment in microneedle patch and needle-free injection technologies for pain-free drug delivery
- 5.7. Surge in subcutaneous delivery systems driving prefillable pen and syringe uptake for chronic disease therapies
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Syringes Market, by Type
- 8.1. Disposable
- 8.2. Reusable
- 9. Syringes Market, by Material
- 9.1. Glass
- 9.2. Plastic
- 9.3. Stainless Steel
- 10. Syringes Market, by Technology
- 10.1. Prefill
- 10.1.1. Auto Injector
- 10.1.2. Cartridge
- 10.2. Safety
- 10.2.1. Active
- 10.2.2. Passive
- 10.3. Smart
- 10.4. Standard
- 11. Syringes Market, by Volume
- 11.1. High Volume
- 11.2. Low Volume
- 11.3. Medium Volume
- 12. Syringes Market, by End User
- 12.1. Hospitals & Clinics
- 12.2. Diagnostic Centers
- 12.3. Blood Banks
- 12.4. Pharmaceutical & Biotech Companies
- 13. Syringes Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Syringes Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Syringes Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. Competitive Landscape
- 16.1. Market Share Analysis, 2024
- 16.2. FPNV Positioning Matrix, 2024
- 16.3. Competitive Analysis
- 16.3.1. Angiplast Pvt. Ltd.
- 16.3.2. Cartel Healthcare Pvt. Ltd
- 16.3.3. Becton, Dickinson and Company
- 16.3.4. GlaxoSmithKline plc
- 16.3.5. AbbVie Inc.
- 16.3.6. Pfizer, Inc.
- 16.3.7. Sanofi S.A.
- 16.3.8. Novartis AG
- 16.3.9. Eli Lilly and Company
- 16.3.10. Terumo Corporation
- 16.3.11. Thermo Fisher Scientific Inc.
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