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Division 7.1.4 Skin irritation

United Kingdom

Original text. Later amendments are not shown.

The results of the study shall provide the potential for skin irritancy of the plant protection product including the potential reversibility of the effects observed.

Before undertaking in vivo studies for corrosion/irritation of the plant protection product, a weight-of-evidence analysis shall be performed on the existing relevant data. Where insufficient data are available, they can be developed through application of sequential testing.

The testing strategy shall follow a tiered approach:

  1. (1)

    the assessment of dermal corrosivity using a validated in vitro test method;

  2. (2)

    the assessment of dermal irritation using a validated in vitro test method (such as human reconstituted skin models);

  3. (3)

    an initial in vivo dermal irritation study using one animal, and where no adverse effects are noted;

  4. (4)

    confirmatory testing using one or two additional animals.

Consideration shall be given to use the dermal toxicity study to provide irritancy information.

Findings of severe skin irritation or corrosion in the dermal study may be used instead of performing a specific irritation study.

  1. Circumstances in which required