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U.S. Early Toxicity Testing Market by Technique (In Vivo, In Vitro, and In Silico), by Toxicity Endpoint (Genotoxicity, Dermal Toxicity, Skin Toxicity, Ocular Toxicity, Phototoxicity, and Others), by End User (Pharmaceutical Industry, Cosmetic Industry, C

U.S. Early Toxicity Testing Market by Technique (In Vivo, In Vitro, and In Silico), by Toxicity Endpoint (Genotoxicity, Dermal Toxicity, Skin Toxicity, Ocular Toxicity, Phototoxicity, and Others), by End User (Pharmaceutical Industry, Cosmetic Industry, C

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U.S. Early Toxicity Testing Market by Technique (In Vivo, In Vitro, and In Silico), by Toxicity Endpoint (Genotoxicity, Dermal Toxicity, Skin Toxicity, Ocular Toxicity, Phototoxicity, and Others), by End User (Pharmaceutical Industry, Cosmetic Industry, Chemical Industry, Food Industry, and Others) – Opportunity Analysis and Industry Forecast, 2023-2030
U.S. Early Toxicity Testing Market was valued at USD 2.42 billion in 2022, and is predicted to reach USD 4.14 billion by 2030, with a CAGR of 6.02% from 2023 to 2030.

In the dynamic landscape of healthcare, a notable paradigm shift has taken root within the United States, which resulted a transformation fueled by the ever-increasing expectations of the population for pharmaceutical solutions that transcend mere functionality. This transformative trend centers around the resolute pursuit of high-quality, potent, and dependable pharmaceutical products that not only meet medical needs but also resonate with the deep-seated desire for safety and efficacy. This palpable shift in consumer aspirations is serving as a transformative force, compelling pharmaceutical enterprises to recalibrate their strategies and invest more assertively in early toxicity testing. In essence, this strategic investment serves as the bedrock upon which the safety and reliability of pharmaceutical products are firmly anchored, thereby fostering a marked expansion of the early toxicity testing market in U.S.

However, stringent regulations set by regulatory bodies such as the US FDA and the EMA require extensive and rigorous testing for drug development and safety, which can be time-consuming and expensive and restrain growth of the market. The complexity and cost of complying with these regulations can pose a significant challenge for small and medium-sized companies that may not have the resources to carry out extensive testing. As a result, some companies may choose to delay or abandon drug development projects, which can limit demand for early toxicity testing services.

Moreover, stringent regulations can also result in a lengthy approval process for new drugs, further delaying the time it takes for drugs to reach the market. This, in turn, is expected to hamper growth of the market.

On the other hand, Introduction of new technologies such as in-vitro modelling using 3D cell culture is expected to provide new lucrative opportunities for the early toxicity testing market during the forecast period. Use of 3D cell cultures can better mimic complexity of tissues and organs, providing more accurate and reliable results for toxicity testing. Traditional 2D cell culture models are limited in their ability to mimic complexity of human tissues and organs, often leading to inaccurate and unreliable results in toxicity testing.

Furthermore, use of 3D cell culture models can better mimic structural and functional complexity of tissues and organs, providing more accurate and reliable results for toxicity testing. 3D cell cultures allow growth and interaction of multiple cell types, creating a microenvironment that more closely resembles human tissues and organs. This can better predict toxic effects of drugs and chemicals in the human body, reducing the risk of adverse effects in clinical trials. Hence, such factors propel the market growth.

Segment Overview

The U.S. early toxicity testing market industry is segmented on the basis of technique, toxicity endpoint, and end user.
• By technique, the market is classified into in vivo, in vitro, and in silico.
• By toxicity endpoint, the market is segmented into genotoxicity, dermal toxicity, skin toxicity, ocular toxicity, phototoxicity, and others.
• By end user, the market is categorized into pharmaceutical industry, cosmetic industry, chemical industry, food industry, and others.

Key Market Players

The key players in the U.S. early toxicity testing market research include companies such as:
• Inotiv Inc.
• Bio-Rad Laboratories Inc
• Evotec A.G.
• Agilent Technologies Inc
• Wuxi Apptec
• Bruker
• Perkinelmer Inc.
• Enzo Biochem Inc.
• Danaher Corporation
• Eurofins Scientific SE
• Charles River Laboratories International, Inc.
• Labcorp Drug Development.
• Promega Corporation
• Insphero AG
• Thermo Fisher Scientific Inc.

KEY BENEFITS
• The U.S. early toxicity testing market report provides a quantitative analysis of the current market and estimations from 2023 to 2030. This analysis assists in identifying the prevailing market opportunities.
• The study comprises a comprehensive analysis of the market trends, including current and future trends for depicting prevalent investment pockets in the market.
• The information related to key drivers, restraints, and opportunities and their impact on the U.S. early toxicity testing market is provided in the report.
• The competitive analysis of the market players along with their market share in the U.S. early toxicity testing market is provided in the report.
• The SWOT analysis and Porter’s Five Forces model are elaborated in the study.
• The value chain analysis in the market study provides a clear picture of the role of stakeholders.

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