9 Amendments of Pilar AYUSO related to 2006/0136(COD)
Amendment 226 #
Article 3 –point 23 a (new)
23a) ‘area of application’ Specific plants, plant species or plant products together with those harmful organisms against which plants and plant products shall be protected or any other purpose for which the plant protection product shall be used;
Amendment 254 #
Article 30 – paragraph 1 - subparagraph 1 a (new)
If no decision concerning the active substance has been made before the provisional period of authorisation for the plant protection product has expired, the Member State may extend this authorisation upon application up to the date when a decision is made on the authorisation of the active substance.
Amendment 256 #
Article 30 – paragraph 2
2. In such cases the Member State may start its evaluation regarding a provisional authorisation as soon as there is evidence that the deadlines for the substance authorisation will not be met and shall immediately inform the other Member States and the Commission of its assessment of the dossier and of the terms of the authorisation, giving at least the information provided for in Article 57 (1).
Amendment 274 #
Article 42 – paragraph 1 - point a
(a) a copy of the authorisation granted by the reference Member State as well as, where requested, a translation of the authorisation into an official or national language of the Member State receiving the application;
Amendment 292 #
Article 63 – paragraph 2 - introductory part
2. Disclosure of the following information shall normally be deemed to undermine the protection of the commercial interests or of privacy and the integrity of the individuals concerned:
Amendment 294 #
Article 67 – paragraph 1 – subparagraph 1
1. Producers, suppliers, distributors, importers, exporters and professional us and importers of plant protection products shall keep records of the plant protection products they produce, import, export, store, use or place on the market for at least three3 years.
Amendment 295 #
Article 80 – paragraph 2 to 4
2. Article 13(1) to (4) and Annexes II and III to Directive 91/414/EEC shall continue to apply with respect to active substances included in Annex I to that Directive and to active substances approved in accordance with paragraph 1 of this Article: (a) date of their inclusion or approval, for active substances covered by Article 8(2) of Directive 91/414/EEC; (b) date of their inclusion or approval, for active substances which were not on the market on 26 July 1993; (c) date of the renewal of the inclusion or renewal of the approval, for active substances whose inclusion in Annex I to Directive 91/414/EEC expires by …. This provision shall only apply to data necess. for a period of five years from the for a period of ten yearys forom the renewal of the approval and which were certified as compliant with the principles of good laboratory practice by that date.for a period of five years from the 3. Where Article 13 of Directive 91/414/EEC applies by virtue of paragraph 1 or paragraph 2 of this Article, it shall be subject to any special rules concerning Directive 91/414/EEC laid down in the Act of Accession by which a Member State joined the Community. 4. the first approval expires by ..., the application provided for in Article 14 shall be submitted by a producer of the active substance to a Member State, with a copy to the other Member States, the Commission and the Authority, no later than two years before the expiry of the first approval.For active substances for which
Amendment 299 #
Article 82
By …...*, Tthe Commission shall present a report to the European Parliament and the Council on the functioning of mutual recognition of authorisations and in particular on the application by the Member States of the provisions referred to in Article 36 (3) and in Article 50 (2), the division of the CommunityEuropean Union into three zones and on the likely future impact of the application of the criteria for the approval of active substances, safeners and synergists as set out in Annex II and the impact thereof on the diversification and competitiveness of agriculture as well as on human health and on the environment. The report may be accompanied, if necessary, by the appropriate legislative proposals to amend those provisions. The criteria as set out in Annex II shall not be applied until after the completion of the process set out in this article. * Note to OJ: 6048 months from the date of entry into force of this Regulation
Amendment 319 #
Annex II - point 3.8.1. a (new)
3.8.1.a. An active substance, safener or synergist shall only be approved if, used under realistic conditions, it does not result in adverse effects on bee colonies. Evaluation must take into account the severity of effects observed under field conditions and the level at which adverse effects are observed on colonies. Uses of an active substance, safener or synergist shall not be authorised if there is evidence, under normal condition of use, that exposure will result in adverse effects on bee colonies.