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In Vitro Toxicity Testing Market Aiming for 10% CAGR, Driven by Bioassay Development by 2030

 


The in vitro toxicity testing market is projected to grow at a CAGR of ~10% over the forecast period. Major factors driving growth include growing investment in research and development for early toxicity detection, rising awareness regarding environmental toxicology and its impact on ecosystems, technological advancement in building innovative toxicology testing models, growing public resistance against animal testing, and rising emphasis on developing personalized medicines. However, the market faces certain limitations, such as the possibility that a substance toxic to a single cell line may not exhibit toxicity at the organ level. This occurs because other cells within the organ might compensate for the imbalance.

In vitro toxicity testing is a scientific approach used to study the adverse effects of chemical, biological, or physical agents on cultured cells or tissues in a controlled laboratory environment. The term "in vitro," meaning "in glass," signifies that these tests are conducted in test tubes, Petri dishes, or similar laboratory setups rather than in a living organism (in vivo). In vitro, tests typically focus on the toxicological processes occurring at the cellular and molecular levels. These studies can provide valuable information, such as metabolic pathways, interactions of active metabolites with cellular and molecular targets, and measurable toxic endpoints that may serve as molecular biomarkers of exposure.

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Growing public resistance against animal testing driving market growth

Public concerns regarding the welfare of animals in research and testing have prompted the implementation of laws and policies designed to minimize or eliminate animal pain and distress. These regulations ensure that animals are used only when scientifically justified and in the smallest numbers necessary to achieve valid scientific results. Currently, in vitro tests often serve as an initial screening tool to assess substances for their mutagenic potential. This aids decision-making on whether in vivo genotoxicity tests are required and, if so, which specific tests to conduct.

In many cases, the availability of in vitro tests has made it possible to avoid in vivo testing altogether during the discovery phase. Moreover, regulatory animal testing may not be required if in vitro genotoxicity tests for chemicals and biocides yield negative results. Additionally, increasing restrictions on animal testing, particularly in regions such as Europe (under REACH regulations) and the US (through FDA modernization initiatives), are significantly driving the growth of in vitro toxicity testing in the market.

Technological advancements in toxicology testing models propel market growth

Advancements in toxicology testing models are revolutionizing the field by enhancing reliability, efficiency, and ethical practices. Emerging technologies such as organoids, artificial intelligence (AI), and omics provide unparalleled insights into human-specific toxicity mechanisms. These innovations reduce reliance on animal models, expedite the development of safer products across industries, and pave the way for more predictive and personalized toxicology approaches. Key trends and cutting-edge technologies driving these advancements include:

  • High-Throughput Screening (HTS): HTS significantly accelerates testing by processing thousands of samples simultaneously using automated robots and microplates. It enables the evaluation of various toxicity endpoints, including cytotoxicity, genotoxicity, and developmental toxicity, in a time-efficient manner
  • Organs-on-Chip (OOC): OOC technology provides a more accurate and realistic method for studying chemical toxicity in human organs and tissues. These microfluidic systems simulate the functions and interactions of multiple organs, offering comprehensive toxicity assessments. Additionally, OOC devices are cost-effective and efficient alternatives to animal testing
  • Systems Toxicology: This approach examines the interactions between molecules and pathways to understand toxicity at a systems level. It aids in identifying new toxicity biomarkers and developing more accurate predictive models, advancing both research and safety evaluations
  • Omics Technologies: Fields such as genomics, proteomics, and metabolomics offer profound insights into the mechanisms of toxicity. These technologies enable a deeper understanding of biological responses to toxic agents and support the identification of molecular biomarkers

Competitive Landscape Analysis

The global in vitro toxicity testing market is marked by the presence of established and emerging market players such as Labcorp Drug Development (formerly Covance); Bio-Rad Laboratories; General Electric Company; Eurofins Scientific SE; BioIVT; Charles River Laboratories International; Thermo Fisher Scientific; Agilent Technologies; Catalent; SGS Group; MB Research Laboratories; Tecan Group; Toxicon Corporation; and Cyprotex; among others. Some of the key strategies adopted by market players include new product development, strategic partnerships and collaborations, and investments.

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Global In Vitro Toxicity Testing Market Segmentation

This report by Medi-Tech Insights provides the size of the global in vitro toxicity testing market at the regional- and country-level from 2023 to 2030. The report further segments the market based on product & service, method, technology, application, and industry.

Market Size & Forecast (2023-2030), By Product & Service, USD Million

  • Consumables
  • Assays
  • Services
  • Equipment
  • Software

Market Size & Forecast (2023-2030), By Method, USD Million

  • Cellular Assays
  • Biochemical Assays
  • Molecular Toxicology Assays
  • Ex-vivo Models
  • In Silico Models

Market Size & Forecast (2023-2030), By Technology, USD Million

  • Cell Culture Technology
  • High Throughput Technology
  • Molecular Imaging Technology
  • OMICS Technology

Market Size & Forecast (2023-2030), By Application USD Million

  • Systemic Toxicology
  • Genotoxicity
  • Cytotoxicity
  • Ocular Toxicity
  • Organ Toxicity
  • Dermal Toxicity
  • Phototoxicity
  • Others

Market Size & Forecast (2023-2030), By Industry USD Million

  • Pharmaceutical & Biopharmaceutical
  • Consumer Care
  • Food
  • Chemical
  • Others

Market Size & Forecast (2023-2030), By Region, USD Million

  • North America
    • US
    • Canada
  • Europe
    • UK
    • Germany
    • Italy
    • Spain
    • Rest of Europe
  • Asia Pacific
    • China
    • India
    • Japan
    • Rest of Asia Pacific
  • Latin America
  • Middle East & Africa

About Medi-Tech Insights

Medi-Tech Insights is a healthcare-focused business research & insights firm. Our clients include Fortune 500 companies, blue-chip investors & hyper-growth start-ups. We have completed 100+ projects in Digital Health, Healthcare IT, Medical Technology, Medical Devices & Pharma Services in the areas of market assessments, due diligence, competitive intelligence, market sizing and forecasting, pricing analysis & go-to-market strategy. Our methodology includes rigorous secondary research combined with deep-dive interviews with industry-leading CXO, VPs, and key demand/supply side decision-makers.

Contact:

Ruta Halde
Associate, Medi-Tech Insights
 +32 498 86 80 79
 info@meditechinsights.com

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