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  2. Developmental toxicity - Wikipedia

    en.wikipedia.org/wiki/Developmental_toxicity

    Developmental toxicity is any developmental malformation that is caused by the toxicity of a chemical or pathogen. It is the structural or functional alteration, reversible or irreversible, which interferes with homeostasis , normal growth , differentiation , development or behavior.

  3. Early Life Stage test - Wikipedia

    en.wikipedia.org/wiki/Early_Life_Stage_test

    An early life stage (ELS) test is a chronic toxicity test using sensitive early life stages like embryos or larvae to predict the effects of toxicants on organisms. [1] ELS tests were developed to be quicker and more cost-efficient than full life-cycle tests, taking on average 1–5 months to complete compared to 6–12 months for a life-cycle test.

  4. Toxicology testing - Wikipedia

    en.wikipedia.org/wiki/Toxicology_testing

    U.S. Army Public Health Center Toxicology Lab technician assessing samples. Toxicology testing, also known as safety assessment, or toxicity testing, is the process of determining the degree to which a substance of interest negatively impacts the normal biological functions of an organism, given a certain exposure duration, route of exposure, and substance concentration.

  5. OECD Guidelines for the Testing of Chemicals - Wikipedia

    en.wikipedia.org/wiki/OECD_Guidelines_for_the...

    Fish, Acute Toxicity Test 204: Fish, Prolonged Toxicity Test: 14-Day Study 205: Avian Dietary Toxicity Test 206: Avian Reproduction Test 207: Earthworm, Acute Toxicity Tests 208: Terrestrial Plant Test: Seedling Emergence and Seedling Growth Test 209: Activated Sludge, Respiration Inhibition Test (Carbon and Ammonium Oxidation) 210: Fish, Early ...

  6. Reference ranges for blood tests - Wikipedia

    en.wikipedia.org/wiki/Reference_ranges_for_blood...

    Reference ranges (reference intervals) for blood tests are sets of values used by a health professional to interpret a set of medical test results from blood samples. Reference ranges for blood tests are studied within the field of clinical chemistry (also known as "clinical biochemistry", "chemical pathology" or "pure blood chemistry"), the ...

  7. Lowest-observed-adverse-effect level - Wikipedia

    en.wikipedia.org/wiki/Lowest-observed-adverse...

    The lowest-observed-adverse-effect level (LOAEL), or the lowest-observed-adverse-effect concentration (LOAEC), is the lowest concentration or amount of a substance found by experiment or observation that causes an adverse alteration of morphology, function, capacity, growth, development, or lifespan of a target organism distinguished from normal organisms of the same species under defined ...

  8. Common Terminology Criteria for Adverse Events - Wikipedia

    en.wikipedia.org/wiki/Common_Terminology...

    The Common Terminology Criteria for Adverse Events (CTCAE), [1] formerly called the Common Toxicity Criteria (CTC or NCI-CTC), are a set of criteria for the standardized classification of adverse events of drugs and treatment used in cancer therapy. The CTCAE system is a product of the US National Cancer Institute (NCI).

  9. In vitro toxicology - Wikipedia

    en.wikipedia.org/wiki/In_vitro_toxicology

    In vitro toxicity testing is the scientific analysis of the toxic effects of chemical substances on cultured bacteria or mammalian cells. [1] In vitro (literally 'in glass') testing methods are employed primarily to identify potentially hazardous chemicals and/or to confirm the lack of certain toxic properties in the early stages of the development of potentially useful new substances such as ...