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Division 7.1 Basic acute toxicity studies

United Kingdom

Original text. Later amendments are not shown.

The studies, data and information to be provided and evaluated, must be sufficient to permit the identification of effects following a single exposure to the plant protection product, and in particular to establish, or indicate:

  • the toxicity of the plant protection product,

  • toxicity of the plant protection product relative to the micro-organism,

  • the time course and characteristics of the effect with full details of behavioural changes and possible gross pathological findings at post-mortem,

  • where possible the mode of toxic action, and

  • the relative hazard associated with the different routes of exposure.

While the emphasis must be on estimating the toxicity ranges involved, the information generated must also permit the plant protection product to be classified in accordance with F1... Regulation (EC) No 1272/2008. The information generated through acute toxicity testing is of particular value in assessing hazards likely to arise in accident situations.

  1. 7.1.1Acute oral toxicity
  2. 7.1.2Acute inhalation toxicity
  3. 7.1.3Acute percutaneous toxicity

Annotations

Textual amendments

F1

Words in Annex Pt. B point 7.1 omitted (31.12.2020) by virtue of The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 22(5)(c)(iv); 2020 c. 1, Sch. 5 para. 1(1)