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Division (ii) In particular, the information provided for the active substance, together with other relevant information, and that provided for one or more preparations containing it shall be sufficient to:F1

United Kingdom

Original text. Later amendments are not shown.

  • decide whether, or not, the active substance can be approved,

  • specify appropriate conditions or restrictions to be associated with any approval,

  • classify the active substance as to hazard,

  • specify the pictograms, signal words and relevant hazard and precautionary statements for the protection of the environment, which are to be included on packaging (containers),

  • predict the distribution, fate, and behaviour in the environment of the active substance and relevant metabolites, degradation and reaction products as well as the times courses involved,

  • identify non-target species and populations for which hazards arise because of potential exposure, and

  • identify measures necessary to minimise contamination of the environment and impact on non-target species.

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Repealed (subject to transitional measures in Arts. 3, 4) by Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active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.