Примеры использования Toxicological data на Английском языке и их переводы на Русский язык
{-}
-
Official
-
Colloquial
The toxicological data should describe the mixture.
There are only limited toxicological data available.
The toxicological data should describe the mixture.
It should be indicated in the SDS whether toxicological data is based on human or animal data. .
Dermal toxicological data was deleted as per comments from WHO.
WHO(1994) and more recently Birnbaum and Staskal(2004) have reviewed the toxicological data on PBDEs in general.
Toxicological data can be also used for defining safe concentrations with regard to the acute risk.
It should be indicated in the SDS whether toxicological data is based on human or animal data. .
Further toxicological data on PM2.5 collected during wildfire smoke episodes in different climates would be useful.
Information on hazard assessment is normally based on internationally accepted toxicological or ecotoxicological data;
It is important to note that toxicological and ecotoxicological data gaps remain with regard to potential alternatives to PFOS and its derivatives.
The original edition, known as the Toxic Substances List was published on June 28, 1971, and included toxicological data for approximately 5,000 chemicals.
The enormous volumes of detailed toxicological data required to establish such levels are beyond the scope of this already broadranging review.
Though the conclusions of the WHO experts are mostlybased on epidemiological evidence, available toxicological data and studies with animals have been thoroughly reviewed as well.
Further toxicological data needed to be gathered based on sound research methodologies, sufficient to permit the determination of a quantifiable toxicological impact.
Given the nature of new psychoactive substances andthe lack of pharmacological and toxicological data on them, it was difficult to determine their long-term health effects.
Compile, share and disseminate information on chemicals of concern to human health and/or the environment in e-products,including summaries of the hazard and toxicological data of these chemicals;
This is done through standardized tests,which may generate toxicological data(for the effects on humans) or eco-toxicological data for the effects on the environment.
This has meant that in order for a new psychoactive substance to be deemed to be legal and obtain market authorization,it must have gone through a rigorous approval process backed up by toxicological data, medical trials etc.
It concluded that,due to the absence of compelling toxicological data about different PM components acting in a complex mixture, it was not possible to quantify the relative importance of the main PM components for effects on human health at this stage.
When the chronic NOEL is compared to environmental exposures for adults from"worse-case" scenario modeling exercises, margin of safety values would be only 0.8-22, orunacceptably low taking into account current deficiencies in the toxicological data base.
Collection of additional toxicological data on endpoints of particular relevance to children, i.e., in utero or post-natal development and growth, and data that would help identify or quantify the extent to which children are exposed to chemicals of concern.
Explore options for improved international cooperation and coordination of research activities aimed at generating, collecting anddisseminating the pharmacological and toxicological data in support of the risk assessments of new psychoactive substances by WHO and regional and national bodies;
Overall, the available toxicological data provide clear evidence that chrysotile fibres can cause a fibrogenic and carcinogenic hazard to humans even though the mechanisms by which chrysotile and other fibres cause fibrogenic and carcinogenic effects are not completely understood.
Therefore, even without data collected from validated endocrine disruptor screening tests(Tier 1 screens and Tier 2 tests),there is a good deal of relevant toxicological data collected from animal testing for endosulfan that has been already performed and evaluated by regulatory bodies as well as independent scientists.
However, a later comparison of the toxicological data and the potential dietary exposure to aldicarb residues in potatoes, carrots, oranges and bananas for adults, young children and infants, as derived by the probabilistic approach at selected high percentiles of the exposure distribution, showed that the estimated exposures were below the Acceptable Daily Intake ADI.
To ask the Secretariat to request a Party that has an enterprise producing a listed new substance to request that enterprise to undertake a preliminary assessment of its ODP following procedures to be developed by the Scientific Assessment Panel and to submit,if available, toxicological data on the listed new substance, and further to request the Party to report the outcome of the request to the Secretariat;
It also reaffirmed that,due to the absence of compelling toxicological data about different PM components acting in the complex ambient PM mixture, it was not possible to precisely quantify the relative importance of the main PM components for effects on human health at this stage.
Paragraph 2 of decision XIII/5 asks the Secretariat to request any Party that has an enterprise producing a new substance to request that enterprise to undertake a preliminary assessment of the ozone-depletion potential of the substance using procedures to be developed by the Scientific Assessment Panel, to submit,if available, toxicological data on the substance, and to report on the outcome of its assessment to the Secretariat.
Differences in the definition of these values in different countries are likely to reflect a range of factors, including:uncertainty in and different interpretations of toxicological data; in-country harmonization of thresholds for different environmental compartments, e.g., of acceptable human intake from air, water and food as well as soil, as defined by ministries of public health; and differences between countries in policy-defined acceptability of risk of harm to humans and other receptors.