Division 1.12 The information provided for the plant protection product and that provided for the active substance, shall be sufficient to:

decide whether, or not, the plant protection product is to be authorised;

specify conditions or restrictions to be associated with any authorisation;

permit an evaluation of short and long-term risks for non-target species, populations, communities and processes;

identify relevant first aid measures as well as appropriate diagnostic and therapeutic measures to be followed in the event of poisoning in humans;

permit a risk assessment of acute and chronic consumer exposure, including, where relevant, a cumulative risk assessment deriving from exposure to more than one active substance;

permit an estimation of acute and chronic exposure to operators, workers, residents and bystanders including, where relevant, the cumulative exposure to more than one active substance;

permit an evaluation to be made as to the nature and extent of the risks for humans, animals (species normally fed and kept by humans or food producing animals) and of the risks for other non-target vertebrate species;

predict the distribution, fate, and behaviour in the environment, as well as the time courses involved;

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

permit an assessment of the impact of the plant protection product on non target species;

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

classify the plant protection product as to hazard in accordance with Regulation (EC) No 1272/2008.