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As per available reports about 20 Conferences, 25 Workshops and 11 Relevant Journals are presently dedicated exclusively to Toxicity Testing and about 480 articles are being published on Toxicity Testing.
Also known as Safety Testing or Toxicology Testing is used to determine the extect to which a substance can cause damage to living or non-living systems. It can be performed by chemical testing methods or animal testing methods. Many products such as drugs, insecticides, artificial flavouring and sweetening agents etc.
OMICS International Organizes 1000+ Global Events inclusive of 300+ Conferences, 500+ Workshops and 200+ Symposiums Every Year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open access journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.
OMICS International Conference Series focuses to enhance knowledge dissemination among its varied range of participants including eminent speakers, renowned scientists, industrialists from top notch companies, young researchers and students. OMICS International Pharma conferences foster the better understanding of latest scientific researches by providing a global exposure to its participants where they can associate with relatable professionals. The scope of these gatherings is further extended by encompassing remarking key areas like Pharmaceutical Regulatory Affairs, Mass Spectrometry, Separation Techniques, Toxicology , Therapeutic Drug Monitoring and Toxicogenomics, Pain Medicine, Clinical Pharmacy, GMP and GLP quality control, followed by Bioavailability and Bioequivalence studies, Biosimilars and Pharmacognosy.
Scope and Importance:
Toxicity studies, conducted to determine the degree to which a substance can damage a living or non-living organisms. It is often conducted by researchers using standard test procedures to comply with governing regulations. Some toxicology testing is chemical testing while some others use animals in the laboratory studies. Toxicity studies can be of, Acute toxicity which involves harmful effects in an organism through a single or short term exposure. Sub-acute toxicity is the ability of a toxic substance to cause effects for more than one year but less than the life time of exposed organism. Chronic toxicity is the ability of the substance or mixture of substances to cause harmful effects over an extended period, usually upon repeated and continuous exposure.
It is essential to use at least two species (usually a rodent and a non- rodent) in the evaluation of the potential toxicity of a drug because species differ in their responses to toxic agents.
The conference on toxicity studies will focus on toxicity testing techniques such as in vivo models and advancements in the development of complex in vitro models, their utility in safety assessment and understanding mechanisms of toxicity, advancing the scientific basis for hazard identification and risk assessment.
An overview of the global toxicity testing market is obtained by analyses of market trends. The two major technology-based approaches utilised are mechanistic and nonmechanistic
In 2011, the global in vitro toxicity testing market was valued at $4 billion and more than $4.9 billion in 2012. This is estimated to reach around $9.9 billion in 2017, with a compound annual growth rate (CAGR) of 14.7% for the five-year period, 2012 to 2017.
Influential factors for this estimation are alternative measures for toxicity and toxicity testing, validation of the techniques for chemicals, pesticides, and food additives.
A significant share of 32% is taken up by the pharmaceutical arena which is valued at $424 million in 2010. This sector is estimated to reach a value of $976 million, at a compound annual growth rate (CAGR) of 18.2%. by 2015.
This page will be updated regularly.
This page was last updated on 15th Sep, 2015
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