Medical Transport Box Market by Product Type (Biological Sample Transport Box, Blood Transport Box, Organ Transport Box), Temperature Control Type (Active, Passive), Material, End User, Sales Channel - Global Forecast 2026-2032
Description
The Medical Transport Box Market was valued at USD 726.63 million in 2025 and is projected to grow to USD 778.48 million in 2026, with a CAGR of 8.53%, reaching USD 1,289.04 million by 2032.
Foundational overview of medical transport solutions contextualizing temperature integrity, materials engineering, regulatory demands, and evolving healthcare distribution networks
The medical transport box landscape underpins critical components of modern healthcare logistics, where the integrity of biological materials and temperature-sensitive therapeutics directly affects clinical outcomes. This introduction frames the essentials of transport packaging technologies, regulatory touchpoints, and the operational contexts-ranging from point-of-care clinics to large hospital systems-where secure cold-chain solutions are mission-critical. Understanding the intersections of materials science, temperature control modalities, and end-user workflows establishes a baseline for interpreting subsequent strategic implications.
Moving beyond elementary descriptions, the narrative here identifies the principal performance attributes that purchasers prioritize, including thermal stability, portability, durability, and compliance with biosafety standards. It also situates the product family within broader healthcare trends such as decentralization of care, the expansion of diagnostic testing outside traditional facilities, and the increasing volume of temperature-sensitive pharmaceuticals. These contextual elements set the stage for deeper analysis of technological shifts, policy impacts, and segmentation-driven opportunities explored in the following sections.
Rapid technological evolution and digitalization driving new expectations for resilience, visibility, and hybrid cold-chain strategies in medical transport systems
The sector is experiencing transformative shifts driven by accelerating demand for resilient cold-chain solutions and rapid innovation in thermal technologies. Active temperature control systems are advancing through compact refrigeration units and long-duration battery systems, while passive options benefit from next-generation insulation materials and phase-change technologies that extend hold times with reduced weight. These technological trajectories are reshaping procurement criteria as purchasers increasingly weigh lifecycle cost, portability, and compatibility with decentralized care models.
Concurrently, regulatory frameworks and public health imperatives are prompting tighter specifications for traceability, temperature monitoring, and incident reporting. The digitalization of logistics-through integrated sensors, blockchain-enabled traceability, and cloud-based monitoring dashboards-has elevated expectations for real-time visibility and proactive exception management. As a result, stakeholders across clinical, laboratory, and distribution channels are reconfiguring workflows to accommodate hybrid solutions that combine active monitoring with engineered passive containment, yielding new service models and value propositions.
Cumulative implications of U.S. tariff adjustments in 2025 driving supply chain localization, input substitution, and strategic sourcing in transport packaging production
Policy changes in tariff regimes can exert concentrated effects across supply chains that source components, insulation materials, and finished packaging from international suppliers. The tariff measures implemented in 2025 have created a set of cumulative pressures that ripple through procurement choices, production cost structures, and supplier selection. Manufacturers that rely on imported metals, composite panels, or specialized vacuum insulation components have faced increased input costs, prompting reassessment of sourcing strategies and prioritization of domestic supply continuity where feasible.
In response, several manufacturers accelerated initiatives to localize key components, reengineer designs to reduce dependency on tariff-impacted inputs, and negotiate longer-term supply agreements to stabilize pricing. Distributors and end users have encountered a more complex procurement environment, where total landed cost and supplier reliability have gained prominence relative to price alone. These shifts have also influenced product roadmaps: design teams are placing greater emphasis on modular architectures that allow substitution of materials without compromising thermal performance, and logistics planners are recalibrating inventory buffers to address episodic supply disruptions while maintaining clinical continuity.
Strategic segmentation analysis revealing how temperature regimes, product typologies, end users, materials, and sales channels interact to shape product and service differentiation
A granular segmentation lens clarifies where innovation and demand converge across product architectures and user needs. Based on Temperature Control Type, the product set is studied across Active and Passive, with Active further delineated into -20°C, -80°C, and 2–8°C applications and Passive subdivided into EPS Foam, PU Foam, and Vacuum Insulation Panel options, which maps directly to clinical use cases and hold-time requirements. Based on Product Type, offerings are classified as Biological Sample Transport Box, Blood Transport Box, Organ Transport Box, and Vaccine Transport Box, each demanding specific design certainties around shock protection, contamination control, and thermal performance.
Based on End User, purchasers include Clinics, Diagnostic Laboratories, Hospitals, and Pharmacies, and each user cohort brings distinct service-level expectations and procurement workflows that influence specification and aftermarket service needs. Based on Material, construction choices span Composite, Fiberglass, Metal, and Plastic, with trade-offs between weight, durability, and insulation performance shaping total cost of ownership calculations. Based on Sales Channel, distribution routes encompass Direct Sales, Distributors, and Online Retail, which vary in terms of customization capability, lead-time assurances, and bundled service offerings. Integrating these segmentation dimensions enables stakeholders to align product strategies with the precise operational and regulatory demands of targeted customer cohorts.
Regional dynamics and logistical realities across the Americas, Europe Middle East & Africa, and Asia-Pacific shaping procurement priorities and product design choices
Regional dynamics influence both product design choices and go-to-market strategies. In the Americas, logistical scale and concentrated healthcare systems create demand for high-throughput solutions and strong after-sales service networks, with emphasis on compatibility with existing cold-chain infrastructures and regulatory compliance frameworks. In Europe, Middle East & Africa, diverse regulatory regimes and a mix of centralized and decentralized healthcare delivery models place a premium on adaptable platforms that can satisfy heterogeneous certification requirements while offering robust traceability.
In Asia-Pacific, rapid expansion of healthcare access, growth in domestic manufacturing capabilities, and an increasing focus on biopharmaceutical distribution have combined to accelerate demand for both high-performance active systems and cost-efficient passive solutions. Across these regions, local procurement policies, tariff regimes, and logistical constraints inform decisions about material selection, insulation technologies, and the balance between off-the-shelf products and tailored engineering. Consequently, regional strategies must harmonize product attributes with prevailing clinical workflows, infrastructure maturity, and regulatory expectations to achieve adoption at scale.
Competitive and collaborative market behaviors revealing how technological differentiation, service models, and channel strategies determine adoption and long-term supplier viability
Competitive dynamics in the medical transport box domain are characterized by a combination of specialized engineering firms, legacy packaging manufacturers, and vertically integrated healthcare suppliers. Many firms pursue differentiation through proprietary insulation technologies, integrated monitoring solutions, and service offerings that extend beyond the physical product to include calibration, validation, and lifecycle support. Partnerships between technology providers and clinical institutions have accelerated the validation of new temperature-control approaches and have reduced time to clinical acceptance by demonstrating operational reliability under real-world conditions.
Investment patterns indicate that product innovation focuses on lightweight high-performance materials, energy-efficient active cooling systems, and embedded connectivity for continuous temperature verification. Meanwhile, manufacturing efficiency and supply chain resilience are rising priorities, prompting strategic alliances with component suppliers and logistics partners. For sellers, the effectiveness of the sales channel-whether direct contracts with large healthcare systems, distributor networks for regional coverage, or digital platforms for smaller purchasers-has become a decisive factor in scaling adoption and delivering differentiated aftermarket services.
Actionable strategic priorities for leaders to combine material innovation, digital monitoring, channel optimization, and supply chain resilience for sustained advantage
Industry leaders should prioritize integrated strategies that combine material innovation, digital monitoring, and supply chain resilience to capture value in an environment defined by regulatory scrutiny and cost pressures. First, accelerate investment in material substitution and modular design approaches that allow rapid interchange of insulation or structural components to mitigate tariff-induced input volatility and to capitalize on advances in vacuum and composite materials. This will reduce exposure to single-sourced inputs and improve adaptability across regional regulatory requirements.
Second, embed digital telemetry and analytics into product offerings to move from reactive to predictive service models; remote temperature monitoring, automated alerts, and cloud-based validation records will become baseline expectations among institutional buyers. Third, recalibrate channel strategies by strengthening distributor partnerships for regional reach while expanding direct engagement for enterprise-level contracts; tailor service-level agreements that reflect the operational realities of clinics, laboratories, hospitals, and pharmacies. Finally, invest in supplier diversification and nearshoring where feasible to shorten lead times and enhance control over quality, thereby improving supply continuity and stakeholder confidence.
Robust mixed-methods research approach integrating stakeholder interviews, technical validation, standards review, and cross-segmentation analysis to underpin conclusions
The research methodology underpinning this analysis combines qualitative stakeholder interviews, technical validation exercises, and a structured review of regulatory guidance and industry standards. Primary inputs included discussions with procurement managers, clinical engineers, product development leads, and logistics coordinators to capture utility-driven preferences, pain points, and real-world performance expectations. Secondary inputs drew on technical literature, standards documentation, and validated component specifications to assess trade-offs between insulation systems, active refrigeration technologies, and structural materials.
Analytical approaches included cross-segmentation mapping to correlate product attributes with end-user requirements and scenario-based supply chain stress testing to evaluate the operational implications of tariff changes and component shortages. Wherever possible, findings were triangulated across multiple sources to enhance robustness and to surface convergent insights rather than relying on single-point observations. This methodology supports practical recommendations while ensuring the conclusions reflect operational realities, regulatory considerations, and technology feasibility assessments.
Synthesis of technological, regulatory, and commercial imperatives that position transport packaging as a strategic clinical enabler rather than a commoditized logistics component
In conclusion, the medical transport box domain is at an inflection point where materials science, digital monitoring, and supply chain strategy converge to redefine procurement and operational practices. Innovations in active refrigeration and advanced passive insulation are expanding the range of feasible use cases, while regulatory attention and tariff dynamics are altering the calculus of sourcing and design. Stakeholders that pursue modular product architectures, invest in telemetry-enabled validation, and shore up supply chains through diversification or nearshoring will be better positioned to meet the exacting demands of clinical operations.
The practical implications for decision-makers are clear: align product roadmaps with the specific thermal, structural, and service needs of target end users; adopt procurement strategies that internalize total lifecycle considerations rather than focusing solely on unit price; and leverage partnerships to accelerate validation and deployment. By synthesizing technological, regulatory, and commercial levers, organizations can transform transport packaging from a cost center into a strategic asset that protects clinical outcomes and supports the expanding reach of temperature-sensitive healthcare delivery.
Note: PDF & Excel + Online Access - 1 Year
Foundational overview of medical transport solutions contextualizing temperature integrity, materials engineering, regulatory demands, and evolving healthcare distribution networks
The medical transport box landscape underpins critical components of modern healthcare logistics, where the integrity of biological materials and temperature-sensitive therapeutics directly affects clinical outcomes. This introduction frames the essentials of transport packaging technologies, regulatory touchpoints, and the operational contexts-ranging from point-of-care clinics to large hospital systems-where secure cold-chain solutions are mission-critical. Understanding the intersections of materials science, temperature control modalities, and end-user workflows establishes a baseline for interpreting subsequent strategic implications.
Moving beyond elementary descriptions, the narrative here identifies the principal performance attributes that purchasers prioritize, including thermal stability, portability, durability, and compliance with biosafety standards. It also situates the product family within broader healthcare trends such as decentralization of care, the expansion of diagnostic testing outside traditional facilities, and the increasing volume of temperature-sensitive pharmaceuticals. These contextual elements set the stage for deeper analysis of technological shifts, policy impacts, and segmentation-driven opportunities explored in the following sections.
Rapid technological evolution and digitalization driving new expectations for resilience, visibility, and hybrid cold-chain strategies in medical transport systems
The sector is experiencing transformative shifts driven by accelerating demand for resilient cold-chain solutions and rapid innovation in thermal technologies. Active temperature control systems are advancing through compact refrigeration units and long-duration battery systems, while passive options benefit from next-generation insulation materials and phase-change technologies that extend hold times with reduced weight. These technological trajectories are reshaping procurement criteria as purchasers increasingly weigh lifecycle cost, portability, and compatibility with decentralized care models.
Concurrently, regulatory frameworks and public health imperatives are prompting tighter specifications for traceability, temperature monitoring, and incident reporting. The digitalization of logistics-through integrated sensors, blockchain-enabled traceability, and cloud-based monitoring dashboards-has elevated expectations for real-time visibility and proactive exception management. As a result, stakeholders across clinical, laboratory, and distribution channels are reconfiguring workflows to accommodate hybrid solutions that combine active monitoring with engineered passive containment, yielding new service models and value propositions.
Cumulative implications of U.S. tariff adjustments in 2025 driving supply chain localization, input substitution, and strategic sourcing in transport packaging production
Policy changes in tariff regimes can exert concentrated effects across supply chains that source components, insulation materials, and finished packaging from international suppliers. The tariff measures implemented in 2025 have created a set of cumulative pressures that ripple through procurement choices, production cost structures, and supplier selection. Manufacturers that rely on imported metals, composite panels, or specialized vacuum insulation components have faced increased input costs, prompting reassessment of sourcing strategies and prioritization of domestic supply continuity where feasible.
In response, several manufacturers accelerated initiatives to localize key components, reengineer designs to reduce dependency on tariff-impacted inputs, and negotiate longer-term supply agreements to stabilize pricing. Distributors and end users have encountered a more complex procurement environment, where total landed cost and supplier reliability have gained prominence relative to price alone. These shifts have also influenced product roadmaps: design teams are placing greater emphasis on modular architectures that allow substitution of materials without compromising thermal performance, and logistics planners are recalibrating inventory buffers to address episodic supply disruptions while maintaining clinical continuity.
Strategic segmentation analysis revealing how temperature regimes, product typologies, end users, materials, and sales channels interact to shape product and service differentiation
A granular segmentation lens clarifies where innovation and demand converge across product architectures and user needs. Based on Temperature Control Type, the product set is studied across Active and Passive, with Active further delineated into -20°C, -80°C, and 2–8°C applications and Passive subdivided into EPS Foam, PU Foam, and Vacuum Insulation Panel options, which maps directly to clinical use cases and hold-time requirements. Based on Product Type, offerings are classified as Biological Sample Transport Box, Blood Transport Box, Organ Transport Box, and Vaccine Transport Box, each demanding specific design certainties around shock protection, contamination control, and thermal performance.
Based on End User, purchasers include Clinics, Diagnostic Laboratories, Hospitals, and Pharmacies, and each user cohort brings distinct service-level expectations and procurement workflows that influence specification and aftermarket service needs. Based on Material, construction choices span Composite, Fiberglass, Metal, and Plastic, with trade-offs between weight, durability, and insulation performance shaping total cost of ownership calculations. Based on Sales Channel, distribution routes encompass Direct Sales, Distributors, and Online Retail, which vary in terms of customization capability, lead-time assurances, and bundled service offerings. Integrating these segmentation dimensions enables stakeholders to align product strategies with the precise operational and regulatory demands of targeted customer cohorts.
Regional dynamics and logistical realities across the Americas, Europe Middle East & Africa, and Asia-Pacific shaping procurement priorities and product design choices
Regional dynamics influence both product design choices and go-to-market strategies. In the Americas, logistical scale and concentrated healthcare systems create demand for high-throughput solutions and strong after-sales service networks, with emphasis on compatibility with existing cold-chain infrastructures and regulatory compliance frameworks. In Europe, Middle East & Africa, diverse regulatory regimes and a mix of centralized and decentralized healthcare delivery models place a premium on adaptable platforms that can satisfy heterogeneous certification requirements while offering robust traceability.
In Asia-Pacific, rapid expansion of healthcare access, growth in domestic manufacturing capabilities, and an increasing focus on biopharmaceutical distribution have combined to accelerate demand for both high-performance active systems and cost-efficient passive solutions. Across these regions, local procurement policies, tariff regimes, and logistical constraints inform decisions about material selection, insulation technologies, and the balance between off-the-shelf products and tailored engineering. Consequently, regional strategies must harmonize product attributes with prevailing clinical workflows, infrastructure maturity, and regulatory expectations to achieve adoption at scale.
Competitive and collaborative market behaviors revealing how technological differentiation, service models, and channel strategies determine adoption and long-term supplier viability
Competitive dynamics in the medical transport box domain are characterized by a combination of specialized engineering firms, legacy packaging manufacturers, and vertically integrated healthcare suppliers. Many firms pursue differentiation through proprietary insulation technologies, integrated monitoring solutions, and service offerings that extend beyond the physical product to include calibration, validation, and lifecycle support. Partnerships between technology providers and clinical institutions have accelerated the validation of new temperature-control approaches and have reduced time to clinical acceptance by demonstrating operational reliability under real-world conditions.
Investment patterns indicate that product innovation focuses on lightweight high-performance materials, energy-efficient active cooling systems, and embedded connectivity for continuous temperature verification. Meanwhile, manufacturing efficiency and supply chain resilience are rising priorities, prompting strategic alliances with component suppliers and logistics partners. For sellers, the effectiveness of the sales channel-whether direct contracts with large healthcare systems, distributor networks for regional coverage, or digital platforms for smaller purchasers-has become a decisive factor in scaling adoption and delivering differentiated aftermarket services.
Actionable strategic priorities for leaders to combine material innovation, digital monitoring, channel optimization, and supply chain resilience for sustained advantage
Industry leaders should prioritize integrated strategies that combine material innovation, digital monitoring, and supply chain resilience to capture value in an environment defined by regulatory scrutiny and cost pressures. First, accelerate investment in material substitution and modular design approaches that allow rapid interchange of insulation or structural components to mitigate tariff-induced input volatility and to capitalize on advances in vacuum and composite materials. This will reduce exposure to single-sourced inputs and improve adaptability across regional regulatory requirements.
Second, embed digital telemetry and analytics into product offerings to move from reactive to predictive service models; remote temperature monitoring, automated alerts, and cloud-based validation records will become baseline expectations among institutional buyers. Third, recalibrate channel strategies by strengthening distributor partnerships for regional reach while expanding direct engagement for enterprise-level contracts; tailor service-level agreements that reflect the operational realities of clinics, laboratories, hospitals, and pharmacies. Finally, invest in supplier diversification and nearshoring where feasible to shorten lead times and enhance control over quality, thereby improving supply continuity and stakeholder confidence.
Robust mixed-methods research approach integrating stakeholder interviews, technical validation, standards review, and cross-segmentation analysis to underpin conclusions
The research methodology underpinning this analysis combines qualitative stakeholder interviews, technical validation exercises, and a structured review of regulatory guidance and industry standards. Primary inputs included discussions with procurement managers, clinical engineers, product development leads, and logistics coordinators to capture utility-driven preferences, pain points, and real-world performance expectations. Secondary inputs drew on technical literature, standards documentation, and validated component specifications to assess trade-offs between insulation systems, active refrigeration technologies, and structural materials.
Analytical approaches included cross-segmentation mapping to correlate product attributes with end-user requirements and scenario-based supply chain stress testing to evaluate the operational implications of tariff changes and component shortages. Wherever possible, findings were triangulated across multiple sources to enhance robustness and to surface convergent insights rather than relying on single-point observations. This methodology supports practical recommendations while ensuring the conclusions reflect operational realities, regulatory considerations, and technology feasibility assessments.
Synthesis of technological, regulatory, and commercial imperatives that position transport packaging as a strategic clinical enabler rather than a commoditized logistics component
In conclusion, the medical transport box domain is at an inflection point where materials science, digital monitoring, and supply chain strategy converge to redefine procurement and operational practices. Innovations in active refrigeration and advanced passive insulation are expanding the range of feasible use cases, while regulatory attention and tariff dynamics are altering the calculus of sourcing and design. Stakeholders that pursue modular product architectures, invest in telemetry-enabled validation, and shore up supply chains through diversification or nearshoring will be better positioned to meet the exacting demands of clinical operations.
The practical implications for decision-makers are clear: align product roadmaps with the specific thermal, structural, and service needs of target end users; adopt procurement strategies that internalize total lifecycle considerations rather than focusing solely on unit price; and leverage partnerships to accelerate validation and deployment. By synthesizing technological, regulatory, and commercial levers, organizations can transform transport packaging from a cost center into a strategic asset that protects clinical outcomes and supports the expanding reach of temperature-sensitive healthcare delivery.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
195 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Definition
- 1.3. Market Segmentation & Coverage
- 1.4. Years Considered for the Study
- 1.5. Currency Considered for the Study
- 1.6. Language Considered for the Study
- 1.7. Key Stakeholders
- 2. Research Methodology
- 2.1. Introduction
- 2.2. Research Design
- 2.2.1. Primary Research
- 2.2.2. Secondary Research
- 2.3. Research Framework
- 2.3.1. Qualitative Analysis
- 2.3.2. Quantitative Analysis
- 2.4. Market Size Estimation
- 2.4.1. Top-Down Approach
- 2.4.2. Bottom-Up Approach
- 2.5. Data Triangulation
- 2.6. Research Outcomes
- 2.7. Research Assumptions
- 2.8. Research Limitations
- 3. Executive Summary
- 3.1. Introduction
- 3.2. CXO Perspective
- 3.3. Market Size & Growth Trends
- 3.4. Market Share Analysis, 2025
- 3.5. FPNV Positioning Matrix, 2025
- 3.6. New Revenue Opportunities
- 3.7. Next-Generation Business Models
- 3.8. Industry Roadmap
- 4. Market Overview
- 4.1. Introduction
- 4.2. Industry Ecosystem & Value Chain Analysis
- 4.2.1. Supply-Side Analysis
- 4.2.2. Demand-Side Analysis
- 4.2.3. Stakeholder Analysis
- 4.3. Porter’s Five Forces Analysis
- 4.4. PESTLE Analysis
- 4.5. Market Outlook
- 4.5.1. Near-Term Market Outlook (0–2 Years)
- 4.5.2. Medium-Term Market Outlook (3–5 Years)
- 4.5.3. Long-Term Market Outlook (5–10 Years)
- 4.6. Go-to-Market Strategy
- 5. Market Insights
- 5.1. Consumer Insights & End-User Perspective
- 5.2. Consumer Experience Benchmarking
- 5.3. Opportunity Mapping
- 5.4. Distribution Channel Analysis
- 5.5. Pricing Trend Analysis
- 5.6. Regulatory Compliance & Standards Framework
- 5.7. ESG & Sustainability Analysis
- 5.8. Disruption & Risk Scenarios
- 5.9. Return on Investment & Cost-Benefit Analysis
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Medical Transport Box Market, by Product Type
- 8.1. Biological Sample Transport Box
- 8.2. Blood Transport Box
- 8.3. Organ Transport Box
- 8.4. Vaccine Transport Box
- 9. Medical Transport Box Market, by Temperature Control Type
- 9.1. Active
- 9.1.1. -20°C
- 9.1.2. -80°C
- 9.1.3. 2–8°C
- 9.2. Passive
- 9.2.1. EPS Foam
- 9.2.2. PU Foam
- 9.2.3. Vacuum Insulation Panel
- 10. Medical Transport Box Market, by Material
- 10.1. Composite
- 10.2. Fiberglass
- 10.3. Metal
- 10.4. Plastic
- 11. Medical Transport Box Market, by End User
- 11.1. Clinics
- 11.2. Diagnostic Laboratories
- 11.3. Hospitals
- 11.4. Pharmacies
- 12. Medical Transport Box Market, by Sales Channel
- 12.1. Direct Sales
- 12.2. Distributors
- 12.3. Online Retail
- 13. Medical Transport Box 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. Medical Transport Box Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Medical Transport Box 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. United States Medical Transport Box Market
- 17. China Medical Transport Box Market
- 18. Competitive Landscape
- 18.1. Market Concentration Analysis, 2025
- 18.1.1. Concentration Ratio (CR)
- 18.1.2. Herfindahl Hirschman Index (HHI)
- 18.2. Recent Developments & Impact Analysis, 2025
- 18.3. Product Portfolio Analysis, 2025
- 18.4. Benchmarking Analysis, 2025
- 18.5. ACH Foam Technologies
- 18.6. Alpha Laboratories
- 18.7. American Aerogel
- 18.8. BioLife Solutions Inc.
- 18.9. Cold Chain Technologies
- 18.10. Cryopak
- 18.11. CSafe Global
- 18.12. DGP Intelsius Limited
- 18.13. Envirotainer
- 18.14. Eppendorf AG
- 18.15. Fresenius Kabi
- 18.16. Inmark Global Holdings, LLC
- 18.17. LMK Thermosafe Ltd.
- 18.18. Pelican BioThermal, Ltd.
- 18.19. Polar Tech Industries
- 18.20. Saudi Basic Industries Corporation
- 18.21. Snyder Industries
- 18.22. Sofrigam
- 18.23. Sonoco ThermoSafe
- 18.24. Tempack Packaging Solutions, S.L.
- 18.25. Temptime Corporation
- 18.26. Thermo Fisher Scientific Inc.
- 18.27. Topa Thermal
- 18.28. TP3 Global
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