11 Amendments of Michèle RIVASI related to 2014/0255(COD)
Amendment 20 #
Proposal for a regulation
Title
Title
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the manufacture, placing on the market and, use of medicated feed and traceability of active substances in the ecosystems and repealing Council Directive 90/167/EEC (Text with EEA relevance)
Amendment 31 #
Proposal for a regulation
Recital 8
Recital 8
(8) Without prejudice to the general obligations laid down in Article 12 of Regulation (EC) No 178/2002 concerning exports of feed to third countries, the provisions of this Regulation should apply to medicated feed and intermediate products which are manufactured, stored, transported or placed on the market within the Union with the intention to be exported. However, the specific requirements concerning labelling, prescription and use of medicated feed and intermediate products should not apply to products intended to be exported. Requirements concerning labelling should not apply where the requirements for labelling are more stringent in the export country than in the EU.
Amendment 42 #
Proposal for a regulation
Recital 13
Recital 13
(13) Labelling of medicated feed should comply with the general principles laid down in Regulation (EC) No 767/2009 and be subject to specific labelling requirements in order to provide the user with the information necessary to correctly administer the medicated feed. Similarly, limits for the deviations of the labelled content of medicated feed from the actual content should be established.
Amendment 54 #
Proposal for a regulation
Recital 17
Recital 17
(17) In order to ensure the safe use of medicated feed, its supply and use should be subject to presentation of a valid veterinary prescription which has been issued after examination of the animals to be treated. However, the possibility to manufacture medicated feed before a prescription is presented to the manufacturer should not be excluded.
Amendment 73 #
Proposal for a regulation
Recital 20 a (new)
Recital 20 a (new)
(20a) A register of the prescriptions of active substances should be kept up to date at the level of competent authorities for water management, for the sake of traceability of the dissemination of chemicals in the ecosystems.
Amendment 80 #
Proposal for a regulation
Article 1 – paragraph 1 – point c
Article 1 – paragraph 1 – point c
(c) the export to third countries of medicated feed and intermediate products. However, Articles 9, 15, 16 and 17 shall not apply to medicated feed and intermediate products whose label indicates that they are intended for export to third countries. Article 9 shall not apply where the requirements for labelling are more stringent in the export country than in the EU.
Amendment 112 #
Proposal for a regulation
Chapter 2 – title
Chapter 2 – title
Manufacture, storage, transport and, placing on the market, traceability of the active substances in the ecosystems
Amendment 144 #
Proposal for a regulation
Article 8
Article 8
Amendment 151 #
Proposal for a regulation
Article 9 – paragraph 3
Article 9 – paragraph 3
Amendment 159 #
Proposal for a regulation
Article 11 a (new)
Article 11 a (new)
Article 11a Traceability of the active substances disseminated in the ecosystems The prescription givers shall fill in a register of the prescriptions of active substances. The register shall be kept up to date at the level of competent authorities for water management, for the sake of traceability of the dissemination of chemicals in the ecosystems.
Amendment 246 #
Proposal for a regulation
Annex 4
Annex 4