OpenLegislation

Division 5.1 Studies on absorption, distribution, excretion and metabolism in mammalsF1

United Kingdom

Original text. Later amendments are not shown.

Quite limited data, as described below and restricted to one test species (normally the rat) may be all that is required in this area. These data can provide information useful in the design and interpretation of subsequent toxicity tests. However, it must be remembered that information on interspecies differences may be crucial in extrapolation of animal data to man and information on percutaneous penetration, absorption, distribution, excretion and metabolism may be useful in operator risk assessments. It is not possible to specify detailed data requirements in all areas, since the exact requirements will be dependent upon the results obtained for each particular test substance.

Aim of the test:

The tests shall provide sufficient data to permit:

  • an evaluation of the rate and extent of absorption,

  • an evaluation of the tissue distribution and the rate and extent of excretion of the test substance and the relevant metabolites,

  • the identification of metabolites and the metabolic pathway.

The effect of dose level on these parameters and whether the results are different after single versus repeated doses, shall also be investigated.

  1. Circumstances in which required
  2. Test guideline

Annotations

Textual amendments

F1

Repealed (subject to transitional measures in Arts. 3, 4) by Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market Text with EEA relevance.