BETA

15 Amendments of Pascal CANFIN related to 2022/0196(COD)

Amendment 434 #
Proposal for a regulation
Recital 15 a (new)
(15a) Manufacturers are key players for the development of alternative to chemical pesticides, whose availability is a necessary step to reach the objectives of this Regulation. It is therefore relevant to ask them to develop a transformation plan, using solid already existing indicators in the EU law, in order to understand how they contribute to the replacement of chemical pesticides with non-chemical alternatives, such as biological control product or services to reduce the use of input or to enhance the uptake of relevant agronomic practices. Such an obligation would enhance transparency of the production of pesticides, and urge manufacturer to switch their business model.
2023/04/04
Committee: ENVI
Amendment 647 #
Proposal for a regulation
Recital 48 a (new)
(48a) In order to support the transition to sustainable food systems and to support the international agreement of the Kunming-Montreal Global Biodiversity Framework, it is important to continue to strengthen the coherence between the European Green Deal, the European Union's sectoral policies and the common trade policy. This coherence requires, in particular, better application of European production standards, in particular sanitary, phytosanitary, environmental and animal welfare standards, to imported products. A variety of tools exist for this purpose at multilateral, bilateral and autonomous level, as noted in the European Commission's report of June 2022, and has to be used in the relevant Regulations and their appropriate application (the Regulation (EC) No 396/2005 on MRLs for instance). This Regulation must contribute to this coherence.
2023/04/04
Committee: ENVI
Amendment 652 #
Proposal for a regulation
Recital 48 b (new)
(48b) Points out that the target 7 of the Kunming-Montreal Global Biodiversity Framework requires parties to tackle the risk of pesticides and highly hazardous chemicals;
2023/04/04
Committee: ENVI
Amendment 2370 #
Proposal for a regulation
Article 25 – paragraph 1 a (new)
1a. Certification schemes shall be delivered only if their associated trainings include proper agronomics training allowing professional users to be able to assess the possibility to use the IPM hierarchy defined in Article 13 every time it is feasible.
2023/04/05
Committee: ENVI
Amendment 2730 #
Proposal for a regulation
Article 43 a (new)Regulation (EU) 1107/2009

Article 9 a (new)
Article 43a Amendments to Regulation (EC) No 1107/2009 In Regulation (EC) No 1107/2009, the following Article 9a is inserted: “Article 9a Horizontal authorization for biological control product The Commission shall permit the extension of the use of biological control product as defined in Article 3(23) of Regulation 2022/196 on a single type of crop to all other crops without the addition of upfront efficacy data.
2023/04/05
Committee: ENVI
Amendment 2731 #
Proposal for a regulation
Article 43 b (new)Regulation (EU) 1107/2009

Article 9 b (new)
Article 43b Amendments to Regulation (EU) 1107/2009 In Regulation (EC) 1107/2009, the following Article 9b is inserted: "Article 9b (new) Priority for biological control product Member States shall apply a priority lane for biological control products as defined in Article 3(23) of Regulation 2022/196 in the application procedure for the approval of an active substance in accordance with Article 7(2) of Regulation (EC) No 1107/2009.”
2023/04/05
Committee: ENVI
Amendment 2732 #
Proposal for a regulation
Article 43 c (new)Regulation (EU) 1107/2009

Article 30
Article 43c Amendments to Regulation (EU) 1107/2009 Article 30 of Regulation (EC) 1107/2009 is replaced by the following: "Article 30 Provisional authorisation at Member State level 1. By way of derogation from Article 29(1)(a), Member States may authorise for a provisional period not exceeding 3 years, the placing on the market of plant protection products containing an biological active substance not yet approved, provided that: (a) the decision on approval could not be finalised within a period of 30 months from the date of admissibility of the application, extended by any additional period set in accordance with Article 9(2), Article 11(3) or Article 12(2) or (3); and (b) pursuant to Article 9se are biological active substances according to the definition in Article 3(23); (b) the dossier on the biological active substance is admissible in relation to the proposed uses pursuant to Article 9; and (c) the Member State concludes that the biological active substance can satisfy the requirements ofcriteria provided for in Article 4(2) and (3) and that the plant protection product may be expected to satisfy the requirements ofin Article 29(1)(b) to (h); and (d) maximum residue levels have been established in accordance with Regulation (EC) No 396/2005. 2. In such cases. 2. In case of a derogation as referred to in paragraph 1, the Member State shall immediately inform the other Member States and the Commission of its assessment of the dossier and of the terms of the authorisation, givincluding at least the information provided for in Article 57(1). 3. The provisions laid down in paragraphs 1 and 2 shall apply until 14 June 2016. If necessary, that time limitIf the Commission decides not to approve the new biological active substance, the Member State which granted the provisional authorisation, or the Commission, shall withdraw that authorisation. 3a. Where a decision on the approval of the new biological active substance has not been adopted by the Commission when the period of three years expires, the Member States which granted the provisional authorisation, or the Commission, may be extended in accordance with the provisional authorisation for a period not exceeding one year, provided that there aregulatory procedure with scrutiny referred to in Article 79(4). good reasons to believe that the biological active substance will satisfy the criteria provided for in Article 4(2) and (3). Member States which extend the provisional authorisation shall inform the other Member States and the Commission of such action.”
2023/04/05
Committee: ENVI
Amendment 2734 #
Proposal for a regulation
Article 43 d (new)
Regulation (EC) No 1107/2009
Article 50 – paragraph 1
1.Article 43d Amendments to Regulation (EU) 1107/2009 In Article 50 of Regulation (EC) No 1107/2009, paragraph 1 is replaced by the following: A comparative assessment shall be 1. performed by Member States when evaluating an application for authorisation for a plant protection product containing an active substance approved as a candidate for substitution. Member States shall not authorise or shall restrict the use of a plant protection product containing a candidate for substitution for use on a particular crop where the comparative assessment weighing up the risks and benefits, as set out in Annex IV, demonstrates that:
2023/04/05
Committee: ENVI
Amendment 2763 #
Proposal for a regulation
Annex I – paragraph 1 – subparagraph 1 – point 1
1. The methodology shall be based on statistics on the quantities of chemical active substances placed on the market in plant protection products under Regulation (EC) No 1107/2009, provided to the Commission (Eurostat) under Annex I to Regulation (EC) No 1185/2009 of the European Parliament and of the Council91 , in combination with a reference hectare application rates calculated by Member States for each active substance on the basis of the maximum dose per hectare in each application, that is set by member states for plant protection products placed on the market containing the respective active substances, in accordance with Article 31 (3) of Regulation (EC) No 1107/2009. __________________ 91 Regulation (EC) No 1185/2009 of the European Parliament and of the Council of 25 November 2009 concerning statistics on pesticides (OJ L 324, 10.12.2009, p. 1).
2023/04/05
Committee: ENVI
Amendment 2771 #
Proposal for a regulation
Annex I – paragraph 1 – subparagraph 1 – point 2 – point e
(e) the chemical active substances in group 4 shall be those not approved under Regulation (EC) No 1107/2009, and therefore not listed in the Annex to Implementing Regulation (EU) No 540/2011;. Active substances in group 4 are assigned the weighting factor corresponding to their group assignment before the loss of approval.
2023/04/05
Committee: ENVI
Amendment 2786 #
Proposal for a regulation
Annex I – Section 1 – Table 1 – Row 4
(iii) 1 8 16 64 1, 8 or 16
2023/04/05
Committee: ENVI
Amendment 2899 #
Proposal for a regulation
Annex VI – Section 2 – point 2 – point e
(e) the active substances in group 4 shall be those not approved under Regulation (EC) No 1107/2009, and therefore not listed in the Annex to Implementing Regulation (EU) No 540/2011;. Active substances in group 4 are assigned the weighting factor corresponding to their group assignment before the loss of approval.
2023/04/05
Committee: ENVI
Amendment 2910 #
Proposal for a regulation
Annex VI – Section 2 – Table 1 – Row 4
(iii) 1 8 16 64 1, 8 or 16
2023/04/05
Committee: ENVI
Amendment 2932 #
Proposal for a regulation
Annex VI – Section 3 – Table 2 – Row 4
(iii) 1 8 16 64 1, 8 or 16
2023/04/05
Committee: ENVI
Amendment 2953 #
Proposal for a regulation
Annex VI – Section 4 – Table 3 – Row 4
(iii) 1 8 16 64 1, 8 or 16
2023/04/05
Committee: ENVI