Dáil Éireann Debate, Tuesday - 23 July 2019
2024. Deputy Michael McGrath asked the Minister for Agriculture, Food and the Marine his views on the practice of spraying glyphosate on food crops before harvest; if work has been carried out to assess the impact of same from a public health perspective; and if he will make a statement on the matter. [32633/19]
Amharc ar fhreagraRegulatory decisions on the approval and use of pesticides are based on the scientific consensus view of all the relevant technical information from all sources. In regard to glyphosate, my Department is guided by the European Food Safety Authority (EFSA) and the European Chemicals Agency (ECHA), who have both concluded, on the basis of extensive reviews, and involving public consultation, that glyphosate can be used safely without putting consumers or users at risk. The EFSA review included an assessment of potential dietary exposure that could result from pre-harvest use. This process guided the decision to renew the authorisation of glyphosate within the European Union in 2017.
Following the approval of active substances at EU level, plant protection products (formulations containing the active ingredient) are assessed thoroughly at a national level on the basis of detailed scientific evaluations conducted in accordance with agreed EU standards and taking account of local agronomic and environmental conditions. This process is currently on-going at Member State level. My Department will only authorise plant protection products on the basis of robust scientific evidence indicating high levels of protection for human and animal health and the environment.
The EU process for consideration of a further renewal of approval of glyphosate will begin in December 2019 and a full dossier will be submitted to the Member States Assessment Group on Glyphosate (France, Hungary, the Netherlands and Sweden) by 15 June 2020. This process will involve a comprehensive scientific evaluation of all relevant data from all sources and will include a public consultation period. My Department will continue to monitor international peer-reviewed scientific evidence and the guidance provided by EFSA and ECHA.
