ADME stands for absorption, distribution, metabolism and
elimination of the drug and chemicals define their nature in a human body.
These four methods define the impact of a specific drug or chemical to the
human tissues. Toxicology testing is an important phenomenon before introducing
new medicine to the market. ADME toxicology facilitated pharmaceutical
manufacturing company to minimize their drug discovery time, testing
complications, and to reduce the cost of drug development.
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Based on the different product type, global ADME-toxicology testing market can be
bifurcated as instruments, software solutions, assays systems, reagents and
others. Based on the technology used in the ADME-toxicology testing the market
can be bifurcated as in-vivo (implemented inside a living organism), and
in-vitro (test performed in a laboratory). Further In-vitro technology is
bifurcated as biochemical testing and cell testing (including liver,
intestinal, kidney). In-vitro technology is expected to witness the highest
growth during the forecast period attributed mainly to the growing concern over
animal rights for using animals for clinical trials.
Asia Pacific is expected to be the fasted growing market of
ADME-Toxicology Testing during the forecast period. The growth is mainly
anticipated from the supporting government initiatives and increasing number of
merger and accusation (M&A) in pharmaceutical companies and research
laboratories.
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Some of the major players operating in the Global
ADME-Toxicology Testing Market include, Accelrys, Inc., Agilent Technologies,
Inc., Caliper Life Sciences, Inc., Bio-Rad Laboratories, Inc., Beckman Coulter,
Inc., Cellartis AB, Cyprotex PLC., Life Technologies Corporation, Optivia
Biotechnology, Inc., Thermo Fisher Scientific, Inc., Molecular Discovery Ltd.,
Cyprotex PLC, MultiCASE, Inc., Promega Corporation, Xceleron, Inc., ACEA
Biosciences, Inc., Albany Molecular Research, Inc., Beckman Coulter, Inc.,
CeeTox, Inc., Molecular Discovery Ltd.
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