The fixed-dose procedure (FDP) was introduced as OECD Test Guideline 420 in 1992, as an alternative to the conventional median lethal dose (LD50) test for the as-sessment of acute oral toxicity (OECD Test Guideline 401). The FDP uses fewer animals and causes less suffering than the conventional test, while providing information on the acute toxicity to allow substances to be ranked according to the EU hazard classification system. Recently the FDP has been revised, with the aim of providing further reductions and refinements, and classification according to the criteria of the Globally Harmonized Hazard Classification and Labelling scheme (GHS). This paper describes the revised FDP and analyses its properties, as determined by a statistical...
AbstractA survey conducted on the EU Notification of New Substances (NONS) database suggested that f...
Acute systemic toxicity data (LD50 values) and hazard classifications derived in the rat following o...
The European Chemicals Agency, ECHA, made available a total of 13,832 oral toxicity studies for 8,56...
The fixed-dose procedure (FDP) was introduced as OECD Test Guideline 420 in 1992, as an alternative ...
The conventional method for the assessment of acute dermal toxicity (OECD Test Guideline 402, 1987) ...
The conventional method for assessing acute oral toxicity (OECD Test Guideline 401) was designed to ...
The conventional method for the assessment of acute inhalation toxicity (OECD Test Guideline 403, 19...
A Guideline 425 is being proposed for evaluation of mammalian acute toxicity to satisfy OECD member ...
The acute oral toxicity test seeks to estimate the dose at which 50 % of the organisms in adefined p...
A new design for acute inhalation toxicity testing was evaluated and compared with results obtained ...
The aim of the present study was to compare the reliability of LD50 determination using the traditio...
Acute inhalation studies are conducted in animals as part of chemical hazard identification and char...
1. Acute toxicity tests are used to evaluate various toxic manifestations following a single exposur...
Acute inhalation studies are conducted in animals as part of chemical hazard identification and char...
[[abstract]]Chemical regulatory authorities around the world require systemic toxicity data from acu...
AbstractA survey conducted on the EU Notification of New Substances (NONS) database suggested that f...
Acute systemic toxicity data (LD50 values) and hazard classifications derived in the rat following o...
The European Chemicals Agency, ECHA, made available a total of 13,832 oral toxicity studies for 8,56...
The fixed-dose procedure (FDP) was introduced as OECD Test Guideline 420 in 1992, as an alternative ...
The conventional method for the assessment of acute dermal toxicity (OECD Test Guideline 402, 1987) ...
The conventional method for assessing acute oral toxicity (OECD Test Guideline 401) was designed to ...
The conventional method for the assessment of acute inhalation toxicity (OECD Test Guideline 403, 19...
A Guideline 425 is being proposed for evaluation of mammalian acute toxicity to satisfy OECD member ...
The acute oral toxicity test seeks to estimate the dose at which 50 % of the organisms in adefined p...
A new design for acute inhalation toxicity testing was evaluated and compared with results obtained ...
The aim of the present study was to compare the reliability of LD50 determination using the traditio...
Acute inhalation studies are conducted in animals as part of chemical hazard identification and char...
1. Acute toxicity tests are used to evaluate various toxic manifestations following a single exposur...
Acute inhalation studies are conducted in animals as part of chemical hazard identification and char...
[[abstract]]Chemical regulatory authorities around the world require systemic toxicity data from acu...
AbstractA survey conducted on the EU Notification of New Substances (NONS) database suggested that f...
Acute systemic toxicity data (LD50 values) and hazard classifications derived in the rat following o...
The European Chemicals Agency, ECHA, made available a total of 13,832 oral toxicity studies for 8,56...