BETA

14 Amendments of Jean-Paul DENANOT related to 2014/0255(COD)

Amendment 101 #
Proposal for a regulation
Article 2 – paragraph 2 – point a
(a) 'medicated feed': a mixture of one or more veterinary medicinal products or one intermediate products with one or more feeds which is ready to be directly fed to animals without further processing, owing to the properties brought by the medicinal part of the mixture for treating or preventing disease and owing to the properties brought by the feed part of the mixture for providing nutrition;
2015/07/02
Committee: AGRI
Amendment 109 #
Proposal for a regulation
Article 2 – paragraph 2 – point f
(f) 'medicated feed business operator': any natural or legal person responsible for ensuring that the requirements of this Regulation are met within the feed business under their control, including brokers and livestock farmers using medicated feed intended for the animals in their possession;
2015/07/02
Committee: AGRI
Amendment 134 #
Proposal for a regulation
Article 2 – paragraph 2 – point i h (new)
(ih) 'medicated feed manufacturer': any medicated feed business operator that manufactures medicated feed;
2015/07/02
Committee: AGRI
Amendment 136 #
Proposal for a regulation
Article 2 – paragraph 2 – point i i (new)
(ii) 'broker': any person active in the buying or selling of medicated feed (excluding the distribution of medicated feed), which operations do not involve the physical handling thereof but rather the trading thereof, independently and in the name of a physical or legal person;
2015/07/02
Committee: AGRI
Amendment 140 #
Proposal for a regulation
Article 3 – paragraph 1
FMedicated feed business operators shall manufacture, store, transport and place on the market medicated feed and intermediate products in compliance with Annex I.
2015/07/02
Committee: AGRI
Amendment 144 #
Proposal for a regulation
Article 3 – paragraph 1 a (new)
1a. A Member State may impose restrictions for prohibiting or regulating the use of mobile mixers in its territory.
2015/07/02
Committee: AGRI
Amendment 147 #
Proposal for a regulation
Article 3 – paragraph 1 c (new)
1c. By way of derogation from paragraph 1, the provisions of Chapter II shall not apply to livestock farmers who only use medicated feed for their own animals.
2015/07/02
Committee: AGRI
Amendment 190 #
Proposal for a regulation
Article 7 – paragraph 2 b (new)
2b. The Commission shall be empowered to adopt implementing acts for establishing criteria in respect of: -the definition of the batch, pursuant to this Article; -the analytical methods that must be employed by medicated feed business operators; -the sampling methods and analytical methods that must be employed by medicated feed business operators and the competent authorities in order to check that the specific carry-over limits have been complied with. Those implementing acts shall be adopted in accordance with the examination procedure referred to in Article 20(2).
2015/07/02
Committee: AGRI
Amendment 192 #
Proposal for a regulation
Article 7 – paragraph 2 c (new)
2c. A detailed schedule listing, in order of priority, the different active substances for which specific carry-over limits must be adopted shall be established by way of an implementing act. The agencies (EFSA and EMA) shall be consulted as the list is being compiled. On [Office of Publications: please insert date counting [24] months from the date of entry into force of this Regulation], the Commission shall submit a report to the European Parliament and to the Council, indicating the specific carry-over limits adopted.
2015/07/02
Committee: AGRI
Amendment 241 #
Proposal for a regulation
Article 15 – paragraph 6 b (new)
6b. Member States may authorise qualified people to prescribe, in accordance with the applicable national laws and pursuant to the conditions set out under Article 10 of Directive 2001/82/CE, medicated feed containing several veterinary medicinal products. However, the prescription of medicated feed containing several veterinary medicinal products comprising one or more antibiotic substances shall not be authorised.
2015/07/02
Committee: AGRI
Amendment 334 #
Proposal for a regulation
Annex 4 – point 1 – paragraph 1
1. The tolerances laid down in this point shall include technical and analytical deviations.
2015/07/02
Committee: AGRI
Amendment 338 #
Proposal for a regulation
Annex 4 – point 1 – paragraph 2
Where the composition of a medicated feed or an intermediate product is found to deviate from the amount of an antimicrobial active substance indicated on the label, a tolerance of ± 10% shall apply. For the other active substances, the following tolerances shall apply:
2015/07/02
Committee: AGRI
Amendment 342 #
Proposal for a regulation
Annex 4 – point 1 – paragraph 2 – table
Active substance per kg of medicated feed Tolerance > 500 mg ± 10% > 10 mg and ≤ 500 mg ± 20% > 0,5 mg and ≤ 10 mg ± 30% > 0,5 mg ± 40% deleted
2015/07/02
Committee: AGRI
Amendment 343 #
Proposal for a regulation
Annex 4 – point 2
2. For the labelling particulars referred to in points 10 and 12 of Annex III to this Regulation, the tolerances laid down in Annex IV to Regulation (EC) No 767/2009 shall apply, as appropriate.deleted
2015/07/02
Committee: AGRI