Clinical Microbiology Market by Product Type (Instruments, Reagents & Kits, Software & Services), Technology (Immunoassays, MALDI-TOF, Microarrays), Application, End User, Specimen Type, Test Type - Global Forecast 2025-2032
Description
The Clinical Microbiology Market was valued at USD 8.68 billion in 2024 and is projected to grow to USD 9.63 billion in 2025, with a CAGR of 11.16%, reaching USD 20.25 billion by 2032.
Comprehensive introduction to the shifting clinical microbiology environment emphasizing technological convergence operational pressures and strategic laboratory priorities
Clinical microbiology is at a pivotal juncture as laboratories, hospitals, and diagnostic developers confront converging technological, regulatory, and economic forces. Advances in molecular methods alongside continued reliance on culture and mass spectrometry have reshaped diagnostic pathways, while digital tools and service models are increasingly integral to laboratory operations. The resulting environment demands that stakeholders reassess workflows, procurement strategies, and talent models in light of faster turnaround expectations and a heightened focus on antimicrobial resistance and infectious disease surveillance.
Laboratories must calibrate investments across instruments, reagents, kits, and software and services to ensure seamless integration and sustainable operations. At the same time, manufacturers face pressure to offer modular solutions and predictable lifecycle support. In practice, this means blending legacy platforms with next-generation sequencing and automation while strengthening data management and maintenance offerings to reduce downtime. Transitioning successfully requires purposeful change management, close alignment between clinical teams and operational leaders, and an emphasis on interoperability to realize both clinical and economic value.
In-depth exploration of transformative trends reshaping diagnostics including platform convergence molecular adoption digital service integration and hybrid clinical workflows
The landscape of clinical microbiology is being transformed by a set of durable shifts that are redefining how diagnostics are developed, validated, and deployed. First, the migration from single-purpose instruments to platform-based solutions has accelerated, enabling laboratories to consolidate workflows and improve throughput. Concurrently, digitalization-from advanced data management software to consulting and maintenance services-has become central to maximizing return on instrumentation and ensuring regulatory compliance. These changes are reinforcing the need for vendors to deliver not only reliable hardware but also integrated software ecosystems and predictable service models.
Another transformative trend is the mainstreaming of high-resolution molecular methods. PCR remains vital for rapid, targeted testing, while sequencing technologies, including high-throughput approaches, are enabling deeper pathogen characterization and genotyping. Mass spectrometry, microarrays, and modern immunoassays continue to play critical roles where speed and cost-effectiveness are paramount. As a result, clinical workflows are evolving toward hybrid diagnostic strategies that combine rapid screening with confirmatory, high-content analyses. Looking ahead, interoperability, modularity, and an outcomes-oriented approach to product development will determine which solutions achieve broad clinical adoption.
Analytical review of how recent United States tariff actions are reshaping procurement sourcing strategies and supply chain resilience across clinical microbiology stakeholders
Recent tariff actions originating in the United States have introduced a series of supply chain and procurement challenges that ripple across clinical microbiology operations and vendor strategies. Increased import levies on equipment components and reagent inputs can elevate landed costs, prompting laboratories and manufacturers to reassess sourcing strategies and inventory management. In response, some suppliers are accelerating localization of critical production steps, diversifying supplier bases, or redesigning packaging and component sourcing to mitigate exposure to tariff volatility. These adaptations help preserve supply continuity but can require capital investment and longer lead times.
For laboratories, the indirect effects can include altered procurement timelines and a renewed emphasis on total cost of ownership rather than purchase price alone. Strategic purchasers are therefore placing greater value on service contracts, reagent security guarantees, and flexible maintenance arrangements that reduce the operational risk of supply disruptions. Moreover, increased trade friction tends to amplify regulatory complexity and administrative overhead for cross-border transfers of diagnostic materials. Consequently, organizations are advised to integrate supply chain risk assessments into clinical and financial planning to maintain diagnostic readiness and operational resilience.
Comprehensive segmentation insights aligning product type technology application end user specimen and test distinctions to actionable development and go to market strategies
Segmentation-based understanding is central to designing product roadmaps and market access strategies. When considering product type, stakeholders must balance investments across instruments, reagents and kits, and software and services, with particular attention to consulting services, data management software, and maintenance and support as growth enablers that extend solution value. Technology choices also drive differentiation; immunoassays spanning CLIA, ELISA, and FIA serve high-volume screening needs, while MALDI-TOF and microarrays provide rapid identification options. PCR retains primacy for targeted diagnostics and sequencing, including both next generation sequencing and traditional Sanger approaches, delivers deep genotyping and outbreak analysis capabilities.
Application-level segmentation highlights divergent demand drivers. Antimicrobial resistance testing, blood screening, genotyping, and infectious disease diagnostics each have unique performance and regulatory requirements. Within infectious diseases, bacterial, fungal, parasitic, and viral infections present distinct analytical challenges and specimen handling needs. End users range from academic research institutes and hospitals and clinics to pharmaceutical and biotech companies and reference laboratories, each requiring tailored service, training, and validation support. Specimen type considerations, including blood with its plasma, serum, and whole blood derivatives, respiratory, tissue, and urine samples, directly influence assay design and pre-analytical workflows. Finally, test type distinctions between qualitative and quantitative outputs inform instrument calibration, reporting systems, and clinical decision support integration. Strategic initiatives that explicitly map product features to these segmentation layers will more effectively address user needs and accelerate adoption.
Strategic regional analysis highlighting how regulatory frameworks procurement behaviors and infrastructure maturity shape diagnostic adoption across global markets
Regional dynamics significantly influence regulatory pathways, procurement preferences, and technology adoption velocities. In the Americas, decision making often prioritizes interoperability, speed of results, and integration with electronic health records, with large hospital networks and reference laboratories driving consolidated purchasing and comprehensive service agreements. Regulatory frameworks and reimbursement approaches shape how assays are validated and adopted, while public health priorities continue to emphasize antimicrobial resistance surveillance and outbreak responsiveness.
Europe, the Middle East and Africa present a mosaic of regulatory environments and infrastructure maturity levels that necessitate adaptable market entry strategies. In some jurisdictions, centralized procurement and stringent conformity assessments encourage vendors to emphasize harmonized quality systems and localized support. Meanwhile, capacity-building initiatives and partnerships with academic institutions remain critical for advancing advanced molecular diagnostics. Asia-Pacific displays rapid technology uptake in metropolitan centers alongside significant investments in scaling laboratory networks; manufacturers and service providers that can offer scalable solutions and robust training programs find favorable traction. Across all regions, attention to local regulatory requirements, supply chain robustness, and culturally attuned commercial engagement is essential for sustainable growth.
Insightful company level analysis showing how modular platforms integrated reagent portfolios and service ecosystems are redefining competitive advantage in diagnostics
Competitive positioning in clinical microbiology increasingly hinges on the ability to combine innovative instrumentation with comprehensive reagent portfolios and enduring service relationships. Market leaders are investing in modular platforms that support multiple assay formats and in expanding software and services offerings, such as consulting, advanced data management, and maintenance contracts, to create recurring revenue streams and deepen customer relationships. Partnerships and alliances are common strategies to bridge capability gaps quickly, enabling faster access to sequencing workflows, automation modules, and laboratory information system integrations.
Another key trend is the elevation of quality assurance and postmarket surveillance capabilities as differentiators. Companies that can demonstrate robust training programs, rapid technical support, and clear documentation for regulatory compliance are better positioned to win large institutional contracts. Moreover, vendors that embrace open architectures and standardized data formats reduce integration friction and enhance long-term customer retention. Observing these priorities can help organizations refine competitive strategies, prioritize R&D investments, and structure commercial offers that align with evolving laboratory procurement criteria.
Actionable recommendations for manufacturers laboratories and service providers to enhance resilience accelerate integration and maximize clinical and commercial impact
Industry leaders must adopt a proactive posture that addresses operational resilience, technology integration, and value realization. First, embedding supply chain risk assessments into product development and procurement planning will reduce exposure to tariff-related disruptions and component shortages. Second, offering bundled solutions that combine instruments with reagents, data management software, and predictable maintenance support can simplify purchasing decisions for large laboratories and health systems. These integrated propositions should be accompanied by clear validation packages and training curricula to accelerate implementation and clinical acceptance.
Third, forging partnerships with clinical networks, public health agencies, and academic centers will expedite real-world performance evaluations and broaden evidence generation for novel assays. Fourth, prioritize interoperability by adopting standardized data formats and APIs to ensure seamless connectivity with laboratory information systems and electronic health records. Finally, invest in scalable service models and remote diagnostics capabilities to minimize downtime and support geographically dispersed laboratory networks. By executing these recommendations, organizations can strengthen their market position, reduce operational risk, and deliver measurable clinical and economic benefits to customers.
Transparent description of research methods including primary stakeholder engagements secondary source triangulation and segmentation driven analytical procedures to ensure robust findings
This research synthesizes primary qualitative engagements with laboratory leaders, procurement officials, and technology developers alongside systematic reviews of regulatory guidance, peer reviewed literature, and product documentation. Primary inputs were structured to capture decision criteria across product acquisition, service expectations, and technology preference, while secondary sources were used to validate technology capabilities and emergent use cases. The methodology emphasizes triangulation of evidence to ensure robustness: vendor-provided technical specifications and clinical validation studies are cross referenced with independent operational reports and expert interviews to mitigate bias.
Analytical procedures included segmentation mapping to align product features with clinical applications, regional regulatory scanning to identify compliance considerations, and scenario analysis to evaluate supply chain exposures under varying trade environments. Qualitative synthesis focused on extracting actionable implications for procurement, product development, and partnership strategies. Throughout, care was taken to document assumptions, preserve traceability of sources, and highlight areas where further primary study could reduce residual uncertainty for decision makers.
Concise conclusion synthesizing technological operational and regulatory priorities that will determine success for laboratories and diagnostic solution providers
In conclusion, clinical microbiology is undergoing a sustained period of evolution driven by technological innovation, shifting commercial models, and external economic pressures. Laboratories and vendors that adopt integrated strategies-combining flexible instrumentation, comprehensive reagent support, and resilient service models-will be better equipped to meet clinical demand and navigate procurement complexities. Digital tools, advanced molecular diagnostics, and careful attention to preanalytical workflows are foundational to improving diagnostic accuracy and turnaround times.
Supply chain resilience and regional regulatory fluency are equally critical; organizations that proactively manage sourcing risks and adapt offerings to local requirements will reduce operational disruptions and accelerate adoption. Finally, an outcomes-oriented approach that emphasizes interoperability, training, and evidence generation will foster trust and sustainable partnerships between manufacturers and end users. These combined priorities form a pragmatic roadmap for stakeholders seeking to drive clinical impact while maintaining commercial viability.
Please Note: PDF & Excel + Online Access - 1 Year
Comprehensive introduction to the shifting clinical microbiology environment emphasizing technological convergence operational pressures and strategic laboratory priorities
Clinical microbiology is at a pivotal juncture as laboratories, hospitals, and diagnostic developers confront converging technological, regulatory, and economic forces. Advances in molecular methods alongside continued reliance on culture and mass spectrometry have reshaped diagnostic pathways, while digital tools and service models are increasingly integral to laboratory operations. The resulting environment demands that stakeholders reassess workflows, procurement strategies, and talent models in light of faster turnaround expectations and a heightened focus on antimicrobial resistance and infectious disease surveillance.
Laboratories must calibrate investments across instruments, reagents, kits, and software and services to ensure seamless integration and sustainable operations. At the same time, manufacturers face pressure to offer modular solutions and predictable lifecycle support. In practice, this means blending legacy platforms with next-generation sequencing and automation while strengthening data management and maintenance offerings to reduce downtime. Transitioning successfully requires purposeful change management, close alignment between clinical teams and operational leaders, and an emphasis on interoperability to realize both clinical and economic value.
In-depth exploration of transformative trends reshaping diagnostics including platform convergence molecular adoption digital service integration and hybrid clinical workflows
The landscape of clinical microbiology is being transformed by a set of durable shifts that are redefining how diagnostics are developed, validated, and deployed. First, the migration from single-purpose instruments to platform-based solutions has accelerated, enabling laboratories to consolidate workflows and improve throughput. Concurrently, digitalization-from advanced data management software to consulting and maintenance services-has become central to maximizing return on instrumentation and ensuring regulatory compliance. These changes are reinforcing the need for vendors to deliver not only reliable hardware but also integrated software ecosystems and predictable service models.
Another transformative trend is the mainstreaming of high-resolution molecular methods. PCR remains vital for rapid, targeted testing, while sequencing technologies, including high-throughput approaches, are enabling deeper pathogen characterization and genotyping. Mass spectrometry, microarrays, and modern immunoassays continue to play critical roles where speed and cost-effectiveness are paramount. As a result, clinical workflows are evolving toward hybrid diagnostic strategies that combine rapid screening with confirmatory, high-content analyses. Looking ahead, interoperability, modularity, and an outcomes-oriented approach to product development will determine which solutions achieve broad clinical adoption.
Analytical review of how recent United States tariff actions are reshaping procurement sourcing strategies and supply chain resilience across clinical microbiology stakeholders
Recent tariff actions originating in the United States have introduced a series of supply chain and procurement challenges that ripple across clinical microbiology operations and vendor strategies. Increased import levies on equipment components and reagent inputs can elevate landed costs, prompting laboratories and manufacturers to reassess sourcing strategies and inventory management. In response, some suppliers are accelerating localization of critical production steps, diversifying supplier bases, or redesigning packaging and component sourcing to mitigate exposure to tariff volatility. These adaptations help preserve supply continuity but can require capital investment and longer lead times.
For laboratories, the indirect effects can include altered procurement timelines and a renewed emphasis on total cost of ownership rather than purchase price alone. Strategic purchasers are therefore placing greater value on service contracts, reagent security guarantees, and flexible maintenance arrangements that reduce the operational risk of supply disruptions. Moreover, increased trade friction tends to amplify regulatory complexity and administrative overhead for cross-border transfers of diagnostic materials. Consequently, organizations are advised to integrate supply chain risk assessments into clinical and financial planning to maintain diagnostic readiness and operational resilience.
Comprehensive segmentation insights aligning product type technology application end user specimen and test distinctions to actionable development and go to market strategies
Segmentation-based understanding is central to designing product roadmaps and market access strategies. When considering product type, stakeholders must balance investments across instruments, reagents and kits, and software and services, with particular attention to consulting services, data management software, and maintenance and support as growth enablers that extend solution value. Technology choices also drive differentiation; immunoassays spanning CLIA, ELISA, and FIA serve high-volume screening needs, while MALDI-TOF and microarrays provide rapid identification options. PCR retains primacy for targeted diagnostics and sequencing, including both next generation sequencing and traditional Sanger approaches, delivers deep genotyping and outbreak analysis capabilities.
Application-level segmentation highlights divergent demand drivers. Antimicrobial resistance testing, blood screening, genotyping, and infectious disease diagnostics each have unique performance and regulatory requirements. Within infectious diseases, bacterial, fungal, parasitic, and viral infections present distinct analytical challenges and specimen handling needs. End users range from academic research institutes and hospitals and clinics to pharmaceutical and biotech companies and reference laboratories, each requiring tailored service, training, and validation support. Specimen type considerations, including blood with its plasma, serum, and whole blood derivatives, respiratory, tissue, and urine samples, directly influence assay design and pre-analytical workflows. Finally, test type distinctions between qualitative and quantitative outputs inform instrument calibration, reporting systems, and clinical decision support integration. Strategic initiatives that explicitly map product features to these segmentation layers will more effectively address user needs and accelerate adoption.
Strategic regional analysis highlighting how regulatory frameworks procurement behaviors and infrastructure maturity shape diagnostic adoption across global markets
Regional dynamics significantly influence regulatory pathways, procurement preferences, and technology adoption velocities. In the Americas, decision making often prioritizes interoperability, speed of results, and integration with electronic health records, with large hospital networks and reference laboratories driving consolidated purchasing and comprehensive service agreements. Regulatory frameworks and reimbursement approaches shape how assays are validated and adopted, while public health priorities continue to emphasize antimicrobial resistance surveillance and outbreak responsiveness.
Europe, the Middle East and Africa present a mosaic of regulatory environments and infrastructure maturity levels that necessitate adaptable market entry strategies. In some jurisdictions, centralized procurement and stringent conformity assessments encourage vendors to emphasize harmonized quality systems and localized support. Meanwhile, capacity-building initiatives and partnerships with academic institutions remain critical for advancing advanced molecular diagnostics. Asia-Pacific displays rapid technology uptake in metropolitan centers alongside significant investments in scaling laboratory networks; manufacturers and service providers that can offer scalable solutions and robust training programs find favorable traction. Across all regions, attention to local regulatory requirements, supply chain robustness, and culturally attuned commercial engagement is essential for sustainable growth.
Insightful company level analysis showing how modular platforms integrated reagent portfolios and service ecosystems are redefining competitive advantage in diagnostics
Competitive positioning in clinical microbiology increasingly hinges on the ability to combine innovative instrumentation with comprehensive reagent portfolios and enduring service relationships. Market leaders are investing in modular platforms that support multiple assay formats and in expanding software and services offerings, such as consulting, advanced data management, and maintenance contracts, to create recurring revenue streams and deepen customer relationships. Partnerships and alliances are common strategies to bridge capability gaps quickly, enabling faster access to sequencing workflows, automation modules, and laboratory information system integrations.
Another key trend is the elevation of quality assurance and postmarket surveillance capabilities as differentiators. Companies that can demonstrate robust training programs, rapid technical support, and clear documentation for regulatory compliance are better positioned to win large institutional contracts. Moreover, vendors that embrace open architectures and standardized data formats reduce integration friction and enhance long-term customer retention. Observing these priorities can help organizations refine competitive strategies, prioritize R&D investments, and structure commercial offers that align with evolving laboratory procurement criteria.
Actionable recommendations for manufacturers laboratories and service providers to enhance resilience accelerate integration and maximize clinical and commercial impact
Industry leaders must adopt a proactive posture that addresses operational resilience, technology integration, and value realization. First, embedding supply chain risk assessments into product development and procurement planning will reduce exposure to tariff-related disruptions and component shortages. Second, offering bundled solutions that combine instruments with reagents, data management software, and predictable maintenance support can simplify purchasing decisions for large laboratories and health systems. These integrated propositions should be accompanied by clear validation packages and training curricula to accelerate implementation and clinical acceptance.
Third, forging partnerships with clinical networks, public health agencies, and academic centers will expedite real-world performance evaluations and broaden evidence generation for novel assays. Fourth, prioritize interoperability by adopting standardized data formats and APIs to ensure seamless connectivity with laboratory information systems and electronic health records. Finally, invest in scalable service models and remote diagnostics capabilities to minimize downtime and support geographically dispersed laboratory networks. By executing these recommendations, organizations can strengthen their market position, reduce operational risk, and deliver measurable clinical and economic benefits to customers.
Transparent description of research methods including primary stakeholder engagements secondary source triangulation and segmentation driven analytical procedures to ensure robust findings
This research synthesizes primary qualitative engagements with laboratory leaders, procurement officials, and technology developers alongside systematic reviews of regulatory guidance, peer reviewed literature, and product documentation. Primary inputs were structured to capture decision criteria across product acquisition, service expectations, and technology preference, while secondary sources were used to validate technology capabilities and emergent use cases. The methodology emphasizes triangulation of evidence to ensure robustness: vendor-provided technical specifications and clinical validation studies are cross referenced with independent operational reports and expert interviews to mitigate bias.
Analytical procedures included segmentation mapping to align product features with clinical applications, regional regulatory scanning to identify compliance considerations, and scenario analysis to evaluate supply chain exposures under varying trade environments. Qualitative synthesis focused on extracting actionable implications for procurement, product development, and partnership strategies. Throughout, care was taken to document assumptions, preserve traceability of sources, and highlight areas where further primary study could reduce residual uncertainty for decision makers.
Concise conclusion synthesizing technological operational and regulatory priorities that will determine success for laboratories and diagnostic solution providers
In conclusion, clinical microbiology is undergoing a sustained period of evolution driven by technological innovation, shifting commercial models, and external economic pressures. Laboratories and vendors that adopt integrated strategies-combining flexible instrumentation, comprehensive reagent support, and resilient service models-will be better equipped to meet clinical demand and navigate procurement complexities. Digital tools, advanced molecular diagnostics, and careful attention to preanalytical workflows are foundational to improving diagnostic accuracy and turnaround times.
Supply chain resilience and regional regulatory fluency are equally critical; organizations that proactively manage sourcing risks and adapt offerings to local requirements will reduce operational disruptions and accelerate adoption. Finally, an outcomes-oriented approach that emphasizes interoperability, training, and evidence generation will foster trust and sustainable partnerships between manufacturers and end users. These combined priorities form a pragmatic roadmap for stakeholders seeking to drive clinical impact while maintaining commercial viability.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
198 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. Rapid multiplex molecular diagnostics enabling same-day pathogen identification and AMR profiling in clinical laboratories
- 5.2. Integration of artificial intelligence platforms for automated colony recognition and antimicrobial susceptibility interpretation in microbiology labs
- 5.3. Expansion of lab automation solutions with robotic specimen processing and digital microbiology informatics to streamline workflows
- 5.4. Growing adoption of point-of-care molecular testing for infectious diseases in emergency and outpatient settings to reduce turnaround times
- 5.5. Increasing use of whole genome sequencing for outbreak investigation and surveillance of hospital-acquired infections at regional reference centers
- 5.6. Development of multiplex respiratory pathogen panels with simultaneous viral and bacterial detection for early clinical decision support
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Clinical Microbiology Market, by Product Type
- 8.1. Instruments
- 8.2. Reagents & Kits
- 8.3. Software & Services
- 8.3.1. Consulting Services
- 8.3.2. Data Management Software
- 8.3.3. Maintenance & Support
- 9. Clinical Microbiology Market, by Technology
- 9.1. Immunoassays
- 9.1.1. CLIA
- 9.1.2. ELISA
- 9.1.3. FIA
- 9.2. MALDI-TOF
- 9.3. Microarrays
- 9.4. PCR
- 9.5. Sequencing
- 9.5.1. NGS
- 9.5.2. Sanger Sequencing
- 10. Clinical Microbiology Market, by Application
- 10.1. Antimicrobial Resistance Testing
- 10.2. Blood Screening
- 10.3. Genotyping
- 10.4. Infectious Diseases
- 10.4.1. Bacterial Infections
- 10.4.2. Fungal Infections
- 10.4.3. Parasitic Infections
- 10.4.4. Viral Infections
- 11. Clinical Microbiology Market, by End User
- 11.1. Academic Research Institutes
- 11.2. Hospitals & Clinics
- 11.3. Pharma & Biotech Companies
- 11.4. Reference Laboratories
- 12. Clinical Microbiology Market, by Specimen Type
- 12.1. Blood
- 12.1.1. Plasma
- 12.1.2. Serum
- 12.1.3. Whole Blood
- 12.2. Respiratory
- 12.3. Tissue
- 12.4. Urine
- 13. Clinical Microbiology Market, by Test Type
- 13.1. Qualitative
- 13.2. Quantitative
- 14. Clinical Microbiology 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. Clinical Microbiology Market, by Group
- 15.1. ASEAN
- 15.2. GCC
- 15.3. European Union
- 15.4. BRICS
- 15.5. G7
- 15.6. NATO
- 16. Clinical Microbiology 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. bioMérieux
- 17.3.2. F. Hoffmann-La Roche Ltd
- 17.3.3. Danaher Corporation
- 17.3.4. Becton, Dickinson and Company
- 17.3.5. Thermo Fisher Scientific Inc
- 17.3.6. Abbott Laboratories
- 17.3.7. Siemens Healthineers AG
- 17.3.8. QIAGEN N.V.
- 17.3.9. Bio-Rad Laboratories, Inc.
- 17.3.10. Bruker Corporation
- 17.3.11. Hologic, Inc.
- 17.3.12. Illumina, Inc.
- 17.3.13. Luminex Corporation
- 17.3.14. PerkinElmer, Inc.
- 17.3.15. Merck KGaA
- 17.3.16. Agilent Technologies, Inc.
- 17.3.17. DiaSorin S.p.A.
- 17.3.18. Ortho Clinical Diagnostics Holdings plc
- 17.3.19. Eurofins Scientific SE
- 17.3.20. Rapid Micro Biosystems, Inc.
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