High Volume Dispensing Systems Market by Technology (Centrifugal Pump Systems, Peristaltic Pump Systems, Reciprocating Pump Systems), Automation Level (Fully Automated Systems, Manual Systems, Semi Automated Systems), Application, End User - Global Foreca
Description
The High Volume Dispensing Systems Market was valued at USD 2.13 billion in 2024 and is projected to grow to USD 2.31 billion in 2025, with a CAGR of 8.49%, reaching USD 4.09 billion by 2032.
An authoritative overview of how high volume dispensing systems have risen to strategic operational importance across life sciences and industrial production ecosystems
High volume dispensing systems are increasingly central to contemporary life sciences and industrial workflows, driving efficiency, repeatability, and safety across a range of laboratory and production environments. These systems span a spectrum from bench-top syringe pumps used for precise reagent additions to integrated, fully automated dispensing suites that interface with upstream and downstream process equipment. As organizations pursue higher throughput, stricter quality controls, and repeatable process performance, the role of robust dispensing platforms has shifted from supporting function to strategic asset.
In parallel, the convergence of regulatory expectations, operational resilience needs, and demands for traceability has elevated the importance of system interoperability and data integrity. Stakeholders across research institutions, biomanufacturing, and clinical diagnostics now prioritize equipment that can deliver validated results, maintain continuity under variable supply conditions, and provide audit-ready records. Consequently, purchasing decisions increasingly weigh total cost of ownership, serviceability, and the ability to adapt to evolving assay formats and reagent chemistries. This introduction sets the stage for a deeper examination of market dynamics, technological inflection points, and pragmatic recommendations for organizations seeking to derive maximum value from high volume dispensing investments.
How advances in automation, digital integration, and materials science are reshaping dispensing system architectures and driving new operational paradigms
The landscape for high volume dispensing systems is undergoing transformative shifts driven by technological innovation, changing customer expectations, and broader trends within life sciences and industrial processing. Automation and advanced motion control have pushed accuracy and throughput to new thresholds, enabling complex protocols and multi-step workflows to be executed with minimal human intervention. Concurrently, the integration of software platforms and laboratory information management systems has turned dispensers into nodes within digital ecosystems, where data capture, provenance, and analytics inform continuous improvement.
Alongside digitalization, material science advances and single-use concepts are prompting redesigns of fluid paths and consumables to reduce cross-contamination risk and accelerate cleaning validation. The emergence of microfluidics and miniaturized dispensing architectures is enabling novel assay formats and reagent economies, while algorithmic control systems and machine learning applications are improving process robustness through predictive maintenance and adaptive dosing. These shifts are not isolated; they create feedback loops where higher automation expectations drive architectural changes in hardware, and new hardware capabilities expand the range of feasible applications.
The discrete ways in which 2025 tariff measures have reshaped sourcing decisions, design tradeoffs, and supplier relationship strategies across dispensing system supply chains
The cumulative impact of tariff actions introduced in 2025 has introduced tangible pressure points across supply chains for high volume dispensing systems, particularly where critical components or subassemblies are sourced internationally. Manufacturers are reassessing supplier footprints to mitigate tariff-induced cost volatility and to preserve margin and competitive positioning. This reassessment frequently leads to strategic sourcing shifts such as dual sourcing, longer-term procurement contracts, and selective nearshoring to reduce exposure to trade policy fluctuations.
In addition to immediate procurement implications, tariffs have prompted design-level responses aimed at substituting tariff-affected materials or components with locally available alternatives, and reengineering assemblies to maintain performance while lowering tariff risk. For buyers, these changes have translated into altered lead times, the need for more rigorous component traceability, and heightened scrutiny of total delivered cost. As organizations adapt, they are prioritizing supplier relationships that offer transparency, flexible manufacturing capacity, and the ability to support regulatory documentation that demonstrates continuity of design and qualification despite supply-side changes.
Actionable segmentation intelligence explaining how application, technology, end user, and automation level intersect to define differentiated customer needs and product priorities
Segmentation analysis reveals differentiated value propositions and adoption patterns across application, technology, end user, and automation level dimensions that inform product strategy and go-to-market approaches. Based on application, systems deployed in biotechnology processes demand rigorous sterility controls and scalable throughput characteristics that differ from clinical diagnostics environments where speed, turnaround, and regulatory traceability are paramount; industrial chemical processing emphasizes chemical compatibility and durability, while laboratory research values flexibility and rapid reconfiguration, and pharmaceutical production prioritizes validated repeatability and regulatory alignment.
Based on technology, centrifugal pump systems offer distinct advantages for continuous flow and shear-sensitive liquids, whereas peristaltic pump systems excel at preserving fluid integrity through disposable tubing and ease of sterilization. Reciprocating pump systems provide high-pressure capability and precise volumetric control for certain formulations, and syringe pump systems deliver the highest level of metered precision for micro- to milliliter-scale dosing. These technology choices intersect with end user profiles, where academic and government laboratories often favor cost-effective, configurable solutions; biotech firms prioritize scalability and pathway to commercialization; contract manufacturing organizations emphasize throughput, repeatability, and documentation to support client projects; pharmaceutical companies demand validated systems that integrate with broader manufacturing execution systems; and research institutions require flexible platforms that support method development.
Based on automation level, fully automated systems are increasingly deployed where continuous operation, reduced manual intervention, and integrated data capture deliver measurable productivity gains, while manual systems retain relevance for low-volume or highly bespoke use cases where cost sensitivity and operator control are primary. Semi automated systems populate a middle ground, enabling incremental automation of critical steps without requiring full process redesign. Understanding these segmentation interactions helps vendors and buyers align product capabilities with the nuanced requirements of each user group and application domain.
Insightful regional analysis illustrating how regulatory frameworks, manufacturing hubs, and service ecosystems shape adoption patterns across the Americas, EMEA, and Asia-Pacific
Regional dynamics exert a powerful influence on technology adoption, procurement strategies, and service delivery models across the global dispensing systems landscape. In the Americas, demand concentrates around innovation hubs and large-scale biomanufacturing clusters where time-to-market pressures and high-throughput needs favor integrated automation and strong aftermarket service networks. Regulatory frameworks and reimbursement landscapes in key jurisdictions drive emphasis on validated performance and traceability, while proximity to OEMs and contract manufacturers supports rapid deployment and service responsiveness.
In Europe, Middle East & Africa, diverse regulatory regimes and a strong emphasis on quality systems encourage modular, interoperable solutions that can be adapted across multiple jurisdictions; established pharmaceutical and diagnostics manufacturers in this region also invest in customization and compliance workflows. In the Asia-Pacific region, rapid capacity expansion, government-driven life sciences initiatives, and a large manufacturing base contribute to strong demand for both scalable automated platforms and cost-effective manual or semi automated options. Supply chain considerations, local manufacturing incentives, and regional standards shape purchasing decisions, encouraging vendors to offer flexible commercial models, regional service centers, and localized validation support to meet distinct market needs.
A strategic assessment of how product modularity, software ecosystems, and service excellence are redefining competitive advantage among dispensing system companies
Competitive dynamics among companies in the high volume dispensing space are characterized by a blend of hardware innovation, software differentiation, and service-led revenue models. Leading organizations invest heavily in modular platform architectures that enable rapid configuration for diverse use cases while protecting intellectual property through unique fluid path designs and control algorithms. Strategic partnerships with software providers, consumable manufacturers, and systems integrators extend product value and create stickier customer relationships through bundled offerings and subscription-style service contracts.
Moreover, companies that excel at delivering predictable uptime and rapid field support often command premium positions, because total cost of ownership considerations increasingly dominate procurement evaluations. Investment in training programs, remote diagnostics, and spare parts logistics underpins this service differentiation. Competitive players are also exploring adjacent moves such as offering assay-validated workflows, co-development agreements with biopharma customers, and certification packages to ease regulatory submissions. These approaches underscore a trend toward verticalizing offerings, where hardware comes pre-integrated with consumables, software, and validation collateral to shorten customer time-to-value.
Clear, prioritized actions for senior leaders to strengthen product adaptability, supply chain resilience, and service-driven revenue in dispensing systems businesses
Industry leaders should prioritize a set of pragmatic actions to capture growth opportunities and insulate operations from systemic risks. First, investing in modular, interoperable hardware designs that support rapid configuration reduces time-to-deployment for new protocols and broadens addressable markets. Complementing hardware investments with open yet secure software integration capabilities enables customers to incorporate dispensing platforms into broader laboratory and production workflows, which in turn enhances product stickiness and data-driven service opportunities.
Second, diversifying supply chains and establishing manufacturing redundancies in low-risk jurisdictions will reduce exposure to tariff and trade policy volatility while improving lead-time resilience. Third, embedding compliance-ready documentation and validation support into product offerings accelerates adoption in regulated environments and lowers customer barriers to procurement. Fourth, enhancing aftermarket and remote service capabilities through predictive diagnostics and outcome-based service agreements improves uptime and creates recurring revenue. Finally, committing to sustainable materials and consumable strategies, such as recyclable tubing options and reduced solvent usage, addresses both regulatory pressures and customer preference evolution, positioning companies as responsible partners in the transition to greener laboratory and production ecosystems.
A transparent explanation of the mixed-methods research approach combining stakeholder interviews, technology assessment, and supply chain mapping to validate findings
The research underpinning these insights combined a structured qualitative and quantitative approach to ensure rigor and relevance. Primary research included interviews with technical decision-makers across academic, commercial, and government laboratories, as well as procurement and engineering leads within manufacturing organizations. These conversations focused on operational constraints, validation requirements, and criteria driving capital and consumable purchasing choices. Secondary research involved systematic review of regulatory guidance documents, product literature, patent filings, white papers, and vendor technical specifications to triangulate claims about performance, compatibility, and intended use cases.
Analytical methods encompassed supply chain mapping to identify concentration risks, technology capability assessments to compare control strategies and fluid handling approaches, and comparative analysis of automation integration patterns across user types. Findings were validated through expert panels and cross-checked against observed procurement behaviors and service contract structures. Quality controls included standardized interview protocols, independent coding of qualitative responses, and versioned documentation of assumptions to ensure transparency and repeatability of the research process.
A strategic synthesis highlighting why dispensing platforms must be treated as integral workflow assets to deliver sustained operational and scientific value
High volume dispensing systems represent a strategic junction where hardware precision, software intelligence, regulatory compliance, and supply chain strategy converge to determine operational outcomes for laboratories and manufacturers. Organizations that approach dispenser selection and deployment holistically-balancing technical fit, data integration, service capability, and sourcing resilience-stand to realize measurable gains in throughput, reproducibility, and cost efficiency. The recent shifts in trade policy and the rapid pace of automation innovation underscore the need for continuous reassessment of procurement practices and vendor partnerships.
In conclusion, the most successful adopters will be those that view dispensing systems not as isolated instruments but as integral components of a broader workflow architecture. By aligning product choices with strategic priorities such as scalability, compliance readiness, and environmental stewardship, stakeholders can turn dispensing investments into durable competitive advantages that support scientific innovation and operational excellence across the lifecycle of assays and production processes.
Note: PDF & Excel + Online Access - 1 Year
An authoritative overview of how high volume dispensing systems have risen to strategic operational importance across life sciences and industrial production ecosystems
High volume dispensing systems are increasingly central to contemporary life sciences and industrial workflows, driving efficiency, repeatability, and safety across a range of laboratory and production environments. These systems span a spectrum from bench-top syringe pumps used for precise reagent additions to integrated, fully automated dispensing suites that interface with upstream and downstream process equipment. As organizations pursue higher throughput, stricter quality controls, and repeatable process performance, the role of robust dispensing platforms has shifted from supporting function to strategic asset.
In parallel, the convergence of regulatory expectations, operational resilience needs, and demands for traceability has elevated the importance of system interoperability and data integrity. Stakeholders across research institutions, biomanufacturing, and clinical diagnostics now prioritize equipment that can deliver validated results, maintain continuity under variable supply conditions, and provide audit-ready records. Consequently, purchasing decisions increasingly weigh total cost of ownership, serviceability, and the ability to adapt to evolving assay formats and reagent chemistries. This introduction sets the stage for a deeper examination of market dynamics, technological inflection points, and pragmatic recommendations for organizations seeking to derive maximum value from high volume dispensing investments.
How advances in automation, digital integration, and materials science are reshaping dispensing system architectures and driving new operational paradigms
The landscape for high volume dispensing systems is undergoing transformative shifts driven by technological innovation, changing customer expectations, and broader trends within life sciences and industrial processing. Automation and advanced motion control have pushed accuracy and throughput to new thresholds, enabling complex protocols and multi-step workflows to be executed with minimal human intervention. Concurrently, the integration of software platforms and laboratory information management systems has turned dispensers into nodes within digital ecosystems, where data capture, provenance, and analytics inform continuous improvement.
Alongside digitalization, material science advances and single-use concepts are prompting redesigns of fluid paths and consumables to reduce cross-contamination risk and accelerate cleaning validation. The emergence of microfluidics and miniaturized dispensing architectures is enabling novel assay formats and reagent economies, while algorithmic control systems and machine learning applications are improving process robustness through predictive maintenance and adaptive dosing. These shifts are not isolated; they create feedback loops where higher automation expectations drive architectural changes in hardware, and new hardware capabilities expand the range of feasible applications.
The discrete ways in which 2025 tariff measures have reshaped sourcing decisions, design tradeoffs, and supplier relationship strategies across dispensing system supply chains
The cumulative impact of tariff actions introduced in 2025 has introduced tangible pressure points across supply chains for high volume dispensing systems, particularly where critical components or subassemblies are sourced internationally. Manufacturers are reassessing supplier footprints to mitigate tariff-induced cost volatility and to preserve margin and competitive positioning. This reassessment frequently leads to strategic sourcing shifts such as dual sourcing, longer-term procurement contracts, and selective nearshoring to reduce exposure to trade policy fluctuations.
In addition to immediate procurement implications, tariffs have prompted design-level responses aimed at substituting tariff-affected materials or components with locally available alternatives, and reengineering assemblies to maintain performance while lowering tariff risk. For buyers, these changes have translated into altered lead times, the need for more rigorous component traceability, and heightened scrutiny of total delivered cost. As organizations adapt, they are prioritizing supplier relationships that offer transparency, flexible manufacturing capacity, and the ability to support regulatory documentation that demonstrates continuity of design and qualification despite supply-side changes.
Actionable segmentation intelligence explaining how application, technology, end user, and automation level intersect to define differentiated customer needs and product priorities
Segmentation analysis reveals differentiated value propositions and adoption patterns across application, technology, end user, and automation level dimensions that inform product strategy and go-to-market approaches. Based on application, systems deployed in biotechnology processes demand rigorous sterility controls and scalable throughput characteristics that differ from clinical diagnostics environments where speed, turnaround, and regulatory traceability are paramount; industrial chemical processing emphasizes chemical compatibility and durability, while laboratory research values flexibility and rapid reconfiguration, and pharmaceutical production prioritizes validated repeatability and regulatory alignment.
Based on technology, centrifugal pump systems offer distinct advantages for continuous flow and shear-sensitive liquids, whereas peristaltic pump systems excel at preserving fluid integrity through disposable tubing and ease of sterilization. Reciprocating pump systems provide high-pressure capability and precise volumetric control for certain formulations, and syringe pump systems deliver the highest level of metered precision for micro- to milliliter-scale dosing. These technology choices intersect with end user profiles, where academic and government laboratories often favor cost-effective, configurable solutions; biotech firms prioritize scalability and pathway to commercialization; contract manufacturing organizations emphasize throughput, repeatability, and documentation to support client projects; pharmaceutical companies demand validated systems that integrate with broader manufacturing execution systems; and research institutions require flexible platforms that support method development.
Based on automation level, fully automated systems are increasingly deployed where continuous operation, reduced manual intervention, and integrated data capture deliver measurable productivity gains, while manual systems retain relevance for low-volume or highly bespoke use cases where cost sensitivity and operator control are primary. Semi automated systems populate a middle ground, enabling incremental automation of critical steps without requiring full process redesign. Understanding these segmentation interactions helps vendors and buyers align product capabilities with the nuanced requirements of each user group and application domain.
Insightful regional analysis illustrating how regulatory frameworks, manufacturing hubs, and service ecosystems shape adoption patterns across the Americas, EMEA, and Asia-Pacific
Regional dynamics exert a powerful influence on technology adoption, procurement strategies, and service delivery models across the global dispensing systems landscape. In the Americas, demand concentrates around innovation hubs and large-scale biomanufacturing clusters where time-to-market pressures and high-throughput needs favor integrated automation and strong aftermarket service networks. Regulatory frameworks and reimbursement landscapes in key jurisdictions drive emphasis on validated performance and traceability, while proximity to OEMs and contract manufacturers supports rapid deployment and service responsiveness.
In Europe, Middle East & Africa, diverse regulatory regimes and a strong emphasis on quality systems encourage modular, interoperable solutions that can be adapted across multiple jurisdictions; established pharmaceutical and diagnostics manufacturers in this region also invest in customization and compliance workflows. In the Asia-Pacific region, rapid capacity expansion, government-driven life sciences initiatives, and a large manufacturing base contribute to strong demand for both scalable automated platforms and cost-effective manual or semi automated options. Supply chain considerations, local manufacturing incentives, and regional standards shape purchasing decisions, encouraging vendors to offer flexible commercial models, regional service centers, and localized validation support to meet distinct market needs.
A strategic assessment of how product modularity, software ecosystems, and service excellence are redefining competitive advantage among dispensing system companies
Competitive dynamics among companies in the high volume dispensing space are characterized by a blend of hardware innovation, software differentiation, and service-led revenue models. Leading organizations invest heavily in modular platform architectures that enable rapid configuration for diverse use cases while protecting intellectual property through unique fluid path designs and control algorithms. Strategic partnerships with software providers, consumable manufacturers, and systems integrators extend product value and create stickier customer relationships through bundled offerings and subscription-style service contracts.
Moreover, companies that excel at delivering predictable uptime and rapid field support often command premium positions, because total cost of ownership considerations increasingly dominate procurement evaluations. Investment in training programs, remote diagnostics, and spare parts logistics underpins this service differentiation. Competitive players are also exploring adjacent moves such as offering assay-validated workflows, co-development agreements with biopharma customers, and certification packages to ease regulatory submissions. These approaches underscore a trend toward verticalizing offerings, where hardware comes pre-integrated with consumables, software, and validation collateral to shorten customer time-to-value.
Clear, prioritized actions for senior leaders to strengthen product adaptability, supply chain resilience, and service-driven revenue in dispensing systems businesses
Industry leaders should prioritize a set of pragmatic actions to capture growth opportunities and insulate operations from systemic risks. First, investing in modular, interoperable hardware designs that support rapid configuration reduces time-to-deployment for new protocols and broadens addressable markets. Complementing hardware investments with open yet secure software integration capabilities enables customers to incorporate dispensing platforms into broader laboratory and production workflows, which in turn enhances product stickiness and data-driven service opportunities.
Second, diversifying supply chains and establishing manufacturing redundancies in low-risk jurisdictions will reduce exposure to tariff and trade policy volatility while improving lead-time resilience. Third, embedding compliance-ready documentation and validation support into product offerings accelerates adoption in regulated environments and lowers customer barriers to procurement. Fourth, enhancing aftermarket and remote service capabilities through predictive diagnostics and outcome-based service agreements improves uptime and creates recurring revenue. Finally, committing to sustainable materials and consumable strategies, such as recyclable tubing options and reduced solvent usage, addresses both regulatory pressures and customer preference evolution, positioning companies as responsible partners in the transition to greener laboratory and production ecosystems.
A transparent explanation of the mixed-methods research approach combining stakeholder interviews, technology assessment, and supply chain mapping to validate findings
The research underpinning these insights combined a structured qualitative and quantitative approach to ensure rigor and relevance. Primary research included interviews with technical decision-makers across academic, commercial, and government laboratories, as well as procurement and engineering leads within manufacturing organizations. These conversations focused on operational constraints, validation requirements, and criteria driving capital and consumable purchasing choices. Secondary research involved systematic review of regulatory guidance documents, product literature, patent filings, white papers, and vendor technical specifications to triangulate claims about performance, compatibility, and intended use cases.
Analytical methods encompassed supply chain mapping to identify concentration risks, technology capability assessments to compare control strategies and fluid handling approaches, and comparative analysis of automation integration patterns across user types. Findings were validated through expert panels and cross-checked against observed procurement behaviors and service contract structures. Quality controls included standardized interview protocols, independent coding of qualitative responses, and versioned documentation of assumptions to ensure transparency and repeatability of the research process.
A strategic synthesis highlighting why dispensing platforms must be treated as integral workflow assets to deliver sustained operational and scientific value
High volume dispensing systems represent a strategic junction where hardware precision, software intelligence, regulatory compliance, and supply chain strategy converge to determine operational outcomes for laboratories and manufacturers. Organizations that approach dispenser selection and deployment holistically-balancing technical fit, data integration, service capability, and sourcing resilience-stand to realize measurable gains in throughput, reproducibility, and cost efficiency. The recent shifts in trade policy and the rapid pace of automation innovation underscore the need for continuous reassessment of procurement practices and vendor partnerships.
In conclusion, the most successful adopters will be those that view dispensing systems not as isolated instruments but as integral components of a broader workflow architecture. By aligning product choices with strategic priorities such as scalability, compliance readiness, and environmental stewardship, stakeholders can turn dispensing investments into durable competitive advantages that support scientific innovation and operational excellence across the lifecycle of assays and production processes.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
192 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. Implementation of AI-powered inline quality inspection in high-volume dispensing workflows for pharmaceutical production
- 5.2. Adoption of robotic arm integration for automated syringing and vial filling in high-speed dispensing lines
- 5.3. Transition to closed-system sterile compounding technologies to meet stringent regulatory compliance in hospital pharmacies
- 5.4. Development of modular high-volume liquid dispensing platforms for customizable biotech research and clinical trial needs
- 5.5. Integration of Internet of Things connectivity for real-time monitoring and predictive maintenance of dispensing equipment
- 5.6. Emergence of disposable cartridge-based dispensing systems to minimize cross-contamination in high-throughput laboratories
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. High Volume Dispensing Systems Market, by Technology
- 8.1. Centrifugal Pump Systems
- 8.2. Peristaltic Pump Systems
- 8.3. Reciprocating Pump Systems
- 8.4. Syringe Pump Systems
- 9. High Volume Dispensing Systems Market, by Automation Level
- 9.1. Fully Automated Systems
- 9.2. Manual Systems
- 9.3. Semi Automated Systems
- 10. High Volume Dispensing Systems Market, by Application
- 10.1. Biotechnology Processes
- 10.2. Clinical Diagnostics
- 10.3. Industrial Chemical Processing
- 10.4. Laboratory Research
- 10.5. Pharmaceutical Production
- 11. High Volume Dispensing Systems Market, by End User
- 11.1. Academic & Government Laboratories
- 11.2. Biotech Firms
- 11.3. Contract Manufacturing Organizations
- 11.4. Pharmaceutical Companies
- 11.5. Research Institutions
- 12. High Volume Dispensing Systems Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. High Volume Dispensing Systems Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. High Volume Dispensing Systems Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. Agilent Technologies, Inc.
- 15.3.2. Analytik Jena GmbH
- 15.3.3. Aurora Biomed Inc.
- 15.3.4. Beckman Coulter, Inc.
- 15.3.5. Bio-Rad Laboratories, Inc.
- 15.3.6. Eppendorf SE
- 15.3.7. Gilson, Inc.
- 15.3.8. Hamilton Company
- 15.3.9. Hudson Robotics, Inc.
- 15.3.10. PerkinElmer, Inc.
- 15.3.11. Sartorius AG
- 15.3.12. SPT Labtech Ltd.
- 15.3.13. Tecan Group Ltd.
- 15.3.14. Thermo Fisher Scientific Inc.
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