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OECD Guidelines for the Testing of Chemicals (OECD TG) are a set of internationally accepted specifications for the testing of chemicals decided on by the Organisation for Economic Co-operation and Development (OECD). They were first published in 1981. They are split into five sections: Section 1: Physical Chemical Properties
The OECD Principles of Good Laboratory Practice (GLP) cover the testing of chemicals or chemical products in non-clinical settings, either in laboratory conditions or environmental settings, such as greenhouses and field experiments. These principles exclude studies involving human subjects.
The Test Methods Regulation is a Regulation (European Union) No. 440/2008 of May 30, 2008. It, and its subsequent amendments, define tests, testing of chemicals for the REACH Regulation . They are based on the OECD Guidelines for the Testing of Chemicals .
In 1998, the FOB was published in the late 1990s as EPA Human Health 870 Series Test Guidelines, [1] [5] [6] and in praxis the Irwin screen and the FOB "overlap and to some extent are interchangeable." [1] The American batteries were harmonised with the OECD's from the same era.
The OECD is responsible for the OECD Guidelines for the Testing of Chemicals, a continuously updated document that is a de facto standard (i.e., soft law). [ 71 ] It published the OECD Environmental Outlook to 2030 in March 2008, which argues that tackling key environmental problems—including climate change , biodiversity loss , water ...
the safety of chemicals, cosmetics, textiles, toys, water pipes, food packaging and other consumer-oriented products; alternatives to animal testing; The BfR is a member of the Working Group of the German Federal Departmental Research Establishments (German: Arbeitsgemeinschaft der Ressortforschungseinrichtungen). [3]
OECD: The Organisation for Economic Co-operation and Development has a Test Guideline program that deals with chemicals. [ 124 ] ICCR : The International Cooperation on Cosmetics Regulation (ICCR) is an international group of cosmetic regulatory authorities from the United States (FDA), Japan (Ministry of Health, Labour, and Welfare), the EU ...
As a result, in 1992 this test was proposed as an alternative to the LD50 test by the Organisation for Economic Co-operation and Development under OECD Test Guideline 420. [4] However, the U.S. Food and Drug Administration has begun to approve non-animal alternatives in response to research cruelty concerns and the lack of validity/sensitivity ...