An important gap has been detected in the application of the European framework for the evaluation of pesticide active substances constituted by enantiomeric and other kind of stereoisomeric mixtures. Up to date, little attention has been paid to the different biological properties of these compounds. Considering efficacy, toxicity, environmental fate and behaviour and ecotoxicity of separated isomers is necessary to fulfil Directive 91/414/EEC objectives of health and environment protection. Here, a critical review of this question for pesticide active substances is presented. An evaluative scheme for considering this question in the framework of Directive 91/414/EEC is also proposed.
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http://dx.doi.org/10.1016/s0045-6535(02)00314-4 | DOI Listing |
According to Article 12 of Regulation (EC) No 396/2005, EFSA has reviewed the maximum residue levels (MRLs) currently established at European level for the pesticide active substance difenoconazole. To assess the occurrence of difenoconazole residues in plants, processed commodities, rotational crops and livestock, EFSA considered the conclusions derived in the framework of Council Directive 91/414/EEC, the MRLs established by the Codex Alimentarius Commission as well as the European authorisations reported by Member States and the UK (including the supporting residues data). Based on the assessment of the available data, MRL proposals were derived, and a consumer risk assessment was carried out.
View Article and Find Full Text PDFRegulation (EC) No 396/2005 establishes the rules governing the setting and the review of pesticide maximum residue levels (MRLs) at European level. According to Article 12(1) of Regulation (EC) No 396/2005, EFSA shall provide within 12 months from the date of the inclusion or non-inclusion of an active substance in Annex I to Directive 91/414/EEC a reasoned opinion on the review of the existing MRLs for that active substance. Among the active substances that need to be reviewed under Article 12(1), EFSA identified two active substances for which a review of MRLs is no longer considered necessary.
View Article and Find Full Text PDFRegulation (EC) No 396/2005 establishes the rules governing the setting and the review of pesticide maximum residue levels (MRLs) at European level. According to Article 12(1) of Regulation (EC) No 396/2005, EFSA shall provide within 12 months from the date of the inclusion or non-inclusion of an active substance in Annex I to Directive 91/414/EEC a reasoned opinion on the review of the existing MRLs for that active substance. Among the substances that need to be reviewed under Article 12(1) of Regulation (EC) No 396/2005, EFSA identified six active substances for which a review of MRLs is no longer considered necessary.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
January 2023
Institut de L'Agriculture et de L'Alimentation Biologiques (ITAB), 149 Rue de BERCY, 75595, PARIS CEDEX 12, France.
With the entry into force of Regulation EC 1107/2009 and the important cut-off of a number of existing active substances from before 2011, which was processed from 342 in Annex I of Directive 91/414/EEC to 298, all these active substances are listed in Part A of Regulation EU 540/2011. Here, we have conducted a survey of all active substances since concerning their regulatory characteristics and their agricultural uses. Between 2011 and 2018, a global increase in active substances was observed with up to 502 approved, but since then an inexorable decline in the number active substances has occurred, despite numerous biocontrol agents (BCAs) being approved and only few chemicals.
View Article and Find Full Text PDFAccording to Article 12 of Regulation (EC) No 396/2005, EFSA has reviewed the maximum residue levels (MRLs) currently established at European level for the pesticide active substance tetraconazole. To assess the occurrence of tetraconazole residues in plants, processed commodities, rotational crops and livestock, EFSA considered the conclusions derived in the framework of Directive 91/414/EEC, as well as the import tolerances and European authorisations reported by Member States and the UK (including the supporting residues data). Based on the assessment of the available data, MRL proposals were derived and a consumer risk assessment was carried out.
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