Примери за използване на Toxicity testing на Английски и техните преводи на Български
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In vitro toxicity testing.
Which have given rise to suspect signs during toxicity testing.
No chronic toxicity testing has been conducted.
IMO 2010FTP Part2 of rule The smoke and toxicity testing procedures.
Short-term toxicity testing on invertebrates(preferred species Daphnia).
Acute Systemic Toxicity Testing.
Short-term toxicity testing on invertebrates(preferred species Daphnia).
The FDA does not consider non-animal alternatives acceptable in reproductive toxicity testing.
In animals, acute toxicity testing is of no relevance as higher doses result in overloading.
The registrant may consider long-term toxicity testing instead of short-term.
Long-term toxicity testing on fish,(unless already provided as part of Annex VIII requirements).
Immunoglobulins are normal constituents of the human body, therefore toxicity testing in heterologous species is of no relevance.
Long-term toxicity testing on plants, unless already provided as part of Annex VII requirements.//.
Now there is a reason to go on and do the epidemiology and the toxicity testing, because these particles are so prolific and people are exposed to them.".
Acute toxicity testing is used to determine the danger of exposure to a chemical by mouth, skin, or inhalation.
That's why biotech companies consult with the Food and Drug Administration about potential GMO foods andperform extensive allergy and toxicity testing.
Reproductive toxicity testing showed no evidence of effects on fertility, embryofoetal, or postnatal development.
If required, follow the specific requirements applicable to difficult to test substances(OECD Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures).
Long-term toxicity testing on fish,(unless already provided as part of Annex VIII requirements).
Where information is not available on a particular ingredient, our laboratories provide access to product toxicity testing to determine whether the ingredient poses a significant risk.
Toxicity testing also helps calculate the No Observed Adverse Effect Level(NOAEL) dose and is helpful for clinical studies.[4].
Nanomaterials are one example,as they may possess unique properties which may require new toxicity testing methods and risk prediction tools from the product development phase onwards, to properly consider safety aspects.
The preclinical toxicity testing on various biological systems reveals the species-, organ- and dose- specific toxic effects of an investigational product.
For substances that have a high potential to adsorb to soil or that are very persistent(Log Kow>5 and/or DT50>180 days or in absence of DT50 the substance is not readily biodegradable),long-term terrestrial toxicity testing according to Annex X is needed instead of short-term testing, even if substance tonnage is at Annex IX(100-1000t/y).
Long-term toxicity testing on invertebrates(preferred species Daphnia),(unless already provided as part of Annex VII requirements)||.
Proposals should capitalise on advances in all relevant fields of science to understand complex biological pathways of toxicological relevance and to identify early markers predictive of toxicological effects in humans with the objectives of developing and validating routine,non-animal approaches for toxicity testing of chemical substances(excluding radio-chemicals).
The information generated through acute toxicity testing is of particular value in assessing hazards likely to arise in accident situations.
Short-term toxicity testing on invertebrates(preferred species Daphnia) The registrant may consider long-term toxicity testing instead of short-term.
Advances in toxicogenomics, bioinformatics, systems biology, epigenetics, andcomputational toxicology are rapidly transforming toxicity testing from a system based on whole-animal testing to one founded primarily on in vitro methods that evaluate changes in biologic processes using cells, cell lines, or cellular components, preferably of human origin.
Long-term toxicity testing shall be proposed by the registrant if the chemical safety assessment according to Annex I indicates the need to investigate further the effects on aquatic organisms.