Healthcare industry can achieve great benefits with Global In-Vitro Toxicology Testing Market research report which brings market and competitive landscape clearly into the focus and assist to make better decisions. The report provides market insights which help gain a more precise understanding of the market landscape, issues that may impose on the Healthcare industry in the future, and how to position specific brands in the best way. Clients can experience a nice combination of best industry insight, practical solutions, talent solutions and latest technology while utilizing or applying the large scale Global In-Vitro Toxicology Testing Market report for the business growth.
Global In-Vitro Toxicology Testing Market research report has complete overview of the market covering various aspects such as product definition, segmentation based on various parameters, and the prevailing vendor landscape.
Data Bridge Market Research analyzes that the global in-vitro toxicology testing market is expected to reach USD 27,952.36 million by 2030, at a CAGR of 12.3% during the forecast period. This market report also covers pricing analysis and technological advancements in depth.
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Market Definition
In-vitro toxicology testing involves testing chemicals, drugs, and other substances to assess their potential toxicity using in-vitro (non-animal) testing methods. In-vitro toxicology testing involves using cells, tissues, or cellular components outside their natural environment to evaluate substances’ safety and potential hazards. The market encompasses a wide range of in-vitro tests and assays that assess various aspects of toxicity, including but not limited to cytotoxicity, genotoxicity, carcinogenicity, organ toxicity, reproductive toxicity, and environmental toxicity. These tests are conducted on cell cultures, tissue models, or other in-vitro systems to mimic the response of biological systems to potential toxicants.
The rapidly growing pharmaceutical and medical device industry
The pharmaceutical and medical device industries have witnessed many revolutionary trends and advances, dramatically improving the medicines available to patients globally. It was possible to witness the effect of artificial intelligence and big data on the diagnosis and treatment of diseases.
Combined with their potential to remedy previously untreatable diseases, biopharmaceutical drugs’ effectiveness, and protection help pharmaceutical companies succeed. An opportunity for sustained healthy growth supports the existing biologics-development pipeline. Since 1995, the number of biotech patents applied annually has increased by 25%. More than 1,500 biomolecules are presently undergoing clinical trials, and the biologics success rate has so far been more than double that of small-molecule drugs, with 13% of biopharmaceuticals entering the phase I testing phase going on to launch.
The pharmaceutical industry relies on in-vitro toxicology testing to assess drug candidates’ safety and potential risks during the early stages of discovery and development. In-vitro testing allows researchers to evaluate the effects of substances on cells, tissues, and organs, providing valuable information on toxicity profiles, drug interactions, and potential side effects. Accurate and reliable toxicity assessments drive the demand for in-vitro toxicology testing in the pharmaceutical industry.
For instance,
The prosperity and growth of these industries proportionally increase the demand for toxicity testing for the quality control of the products developed by them. Therefore, the rapidly growing pharmaceutical and medical device industries act as a driver for the growth of the market.
Market Developments
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Major Players
Data Bridge Market Research recognizes the following companies as the market players in the global in-vitro toxicology testing market Thermo Fisher Scientific Inc. (U.S.), Labcorp Drug Development (U.S.), Merck KGaA (Germany), Charles River Laboratories (U.S.), Lonza (Switzerland), Bio-Rad Laboratories, Inc. (U.S.), Catalent, Inc (U.S.), SGS Société Générale de Surveillance SA (Switzerland), QIAGEN (Germany), Intertek Group plc. (U.K.), Eurofins Scientific (Luxembourg), Promega Corporation (U.S.), Aragen Life Sciences Ltd. (India), Cyprotex Plc. (U.K.), Shanghai Medicilon Inc. (China), Creative Biolabs (U.S.), BioIVT (U.S.), AAT Bioquest, Inc. (U.S.), Gentronix (UK), IONTOX (U.S.), InSphero (U.S.), MB Research Laboratories (U.S.), Creative Bioarray (U.S.), and Preferred Cell Systems (U.S.) among others.
Segment Analysis:
The global in-vitro toxicology testing market is segmented into six notable segments such as product and service, toxicology end point and test, technology, method, industry, and distribution channel.
In 2023, the consumables segment is expected to dominate the global in-vitro toxicology testing market
In 2023, the consumables segment is expected to dominate the market with a market share of 34.33% and growing with a CAGR of 13.7% from 2023 to 2030. It is expected to dominate the market due to its increasing demand among the population.
In 2023, the pharmaceutical and biopharmaceutical companies segment is expected to dominate the global in-vitro toxicology testing market
In 2023, the pharmaceutical and biopharmaceutical companies segment is expected to dominate the market with a market share of 33.81% and grow with a CAGR of 13.7% from 2023 to 2030. It is expected to dominate the market due to the growing demand for personalized medicines and precision toxicology
Report Scope and Market Segmentation
Report Metric | Details |
Forecast Period | 2023 to 2030 |
Base Year | 2022 |
Historic Years | 2021 (Customisable to 2015-2020) |
Quantitative Units | Revenue in USD Million, Volumes in Units, and Pricing in USD |
Top Key Topics Covered:
Continued…
Fundamental Aim of this Market Report
Key highlights of this Market report:
TOC:
1 INTRODUCTION
1.1 OBJECTIVES OF THE STUDY
1.2 MARKET DEFINITION
1.3 OVERVIEW OF THE GLOBAL IN-VITRO TOXICOLOGY TESTING MARKET
1.4 CURRENCY AND PRICING
1.5 LIMITATIONS
1.6 MARKETS COVERED
2 MARKET SEGMENTATION
2.1 MARKETS COVERED
2.2 GEOGRAPHICAL SCOPE
2.3 YEARS CONSIDERED FOR THE STUDY
2.4 DBMR TRIPOD DATA VALIDATION MODEL
2.5 PRIMARY INTERVIEWS WITH KEY OPINION LEADERS
2.6 MULTIVARIATE MODELLING
2.7 PRODUCT AND SERVICE SEGMENT LIFELINE CURVE
2.8 MARKET END USER COVERAGE GRID
2.9 DBMR MARKET POSITION GRID
2.1 VENDOR SHARE ANALYSIS
2.11 SECONDARY SOURCES
2.12 ASSUMPTIONS
3 EXECUTIVE SUMMARY
4 PREMIUM INSIGHTS
4.1 PESTEL ANALYSIS
4.2 PORTERS ANALYSIS
5 GLOBAL IN-VITRO TOXICOLOGY TESTING MARKET, INDUSTRY INSIGHTS
6 GLOBAL IN-VITRO TOXICOLOGY TESTING MARKET, REGULATIONS
7 MARKET OVERVIEW
8 GLOBAL IN-VITRO TOXICOLOGY TESTING MARKET, BY PRODUCT AND SERVICE
9 GLOBAL IN-VITRO TOXICOLOGY TESTING MARKET, BY TOXICOLOGY ENDPOINT AND TEST
Continued…
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