North America Toxicology Laboratories Market Analysis-2027

NORTH AMERICA TOXICOLOGY LABORATORIES MARKET ANALYSIS INDUSTRY INSIGHTS, TRENDS, OUTLOOK, AND OPPORTUNITY ANALYSIS, 2020–2027

REPORT DESCRIPTION North America Toxicology Laboratories Market - Overview The various instruments, reagents, and kits used to diagnose the amount of substance across forensic laboratories (public and private), rehabilitation centers, hospitals and trauma centers, and diagnostics laboratories include, ELISA kit, PCR kit, Enzyme Multiplied Immunoassay Technique (EMIT), RIA, immunochemistry analyzers, PCR machine, gas chromatography (GC)-mass spectrometry (MS), and high performance liquid chromatography (HPLC). Statistics: North America toxicology laboratories market is estimated to account for US$ 317.1 Mn in terms of value by the end of 2027 North America Toxicology Laboratories Market: Drivers Stringent regulatory scenario on consumption of controlled substances is expected to propel growth of North America toxicology laboratories market. For instance, the U.S. Controlled Substances Act controls the manufacturing, distribution, and dispensing of controlled substances across the U. S. North America Toxicology Laboratories Market: Opportunities Key players in the market can focus on the use of enhancing production technology to offer cheaper kits and instruments for toxicology laboratories. For instance, in December 2019, InSphero AG announced upgrades to its production technology that decreased the cost of its assay-ready 3D InSight Human Liver Microtissues.

REPORT DESCRIPTION North America Toxicology Laboratories Market: Restraints The conventional technologies used to detect the presence of abusive substances require a large amount of sample, which is difficult to procure in critical situations. This is expected to hamper growth of North America toxicology laboratories market. Key Takeaways: The Urine sample segment in North America toxicology laboratories market was valued at US$ 75.9 Mn in 2018 and is expected to reach US$ 189.2 Mn by 2027 at a CAGR of 10.3% during the forecast period. The growth of the segment is anticipated to increasing demand for toxicology testing and increasing consumption of controlled substances in North America.

The Forensic Laboratories segment held dominant position in North America toxicology laboratories market in 2018, accounting for 46.2% share in terms of value, followed by diagnostic laboratories respectively. The growth of the segment is attributed to increasing technological advancements such as integration of cloud computing during the forecast period. The market is witnessing increasing M&A activities from major market players. For instance, in June 2019, Eurofins Scientific acquired Transplant Genomics Inc., a molecular diagnostics company focused on enhancing organ transplant outcomes with non-invasive serial monitoring guided by genomics. Request a Sample copy of this reports : https://www.coherentmarketinsights.com/insight/request-sample/3277 ÂŠ Coherent market Insights. All Rights Reserved

REPORT DESCRIPTION Regulations According to the U.S. FDA, “the pre-market notifications are required when the laboratory automation system are hands-off the sample ID directly to the analyzer, without the analyzer performing sample identification.” If the devices perform simple physiological and clinical calculations, the pre-market notification is not required North America Toxicology Laboratories Market: Competitive Landscape

Major players operating in North America toxicology laboratories market include, InSphero AG, The Charles Stark Draper Laboratory, Inc., Bristol-Myers Squibb Company, Thermo Fisher Scientific Inc., Agilent Technologies, Inc., Bio Rad Laboratories Inc., Eurofins Scientific, Neogen Corporation, Enzo Life Sciences, Inc., and Vala Sciences Inc. North America Toxicology Laboratories Market: Key Developments In December 2019, Thermo Fisher Scientific Inc. started its new viral vector contract development and manufacturing organization site in Lexington, Massachusetts. The 50,000-square-foot facility is expected to support the development, testing, and manufacture of viral vectors.

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