8 Amendments of Norbert ERDŐS related to 2014/0255(COD)
Amendment 49 #
Proposal for a regulation
Recital 9
Recital 9
(9) Medicated feed should be manufactured only with authorised veterinary medicinal products and the compatibility of all compounds used should be ensured for the purpose of safety and efficacy of the product. The holder of the authorisation of the veterinary medicinal products is responsible for compatibility assessment. Additional specific requirements or instructions for the inclusion of the veterinary medicinal products into feed should be foreseen to ensure a safe and efficient treatment of the animals.
Amendment 57 #
Proposal for a regulation
Recital 14
Recital 14
Amendment 112 #
Proposal for a regulation
Article 2 – paragraph 2 – point h
Article 2 – paragraph 2 – point h
Amendment 175 #
Proposal for a regulation
Article 7 – paragraph 2 – subparagraph 1
Article 7 – paragraph 2 – subparagraph 1
The Commission shall be empowered to adopt delegated acts in accordance with Article 19 concerning the establishment of specific carry-over limits for active substances. Limits shall be based on the opinion of the European Food Safety Authority.
Amendment 188 #
Proposal for a regulation
Article 7 – paragraph 2 – subparagraph 2 – point b
Article 7 – paragraph 2 – subparagraph 2 – point b
(b) for the other active substances, 3% of the maximum permitted dose of the active substance in the last batch of medicated feed or ofin intermediate product produced before the production of non- target feed.
Amendment 206 #
Proposal for a regulation
Article 10 – paragraph 1
Article 10 – paragraph 1
Medicated feed and intermediate products shall be placed on the market only in sealed packages – including sack packaging – or containers. Packages or containers shall be sealed in such a way that, when the package or container is opened, the seal is damaged and cannot be reused.
Amendment 276 #
Proposal for a regulation
Article 16 – paragraph 4
Article 16 – paragraph 4
Amendment 340 #
Proposal for a regulation
Annex 4 – point 1 – paragraph 2
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: Active substance per kg of Tolerance medicated feed > 500 mg • ± 20% > 100 mg and ≤ 500 mg • ± 25% > 10 mg and ≤ 100 mg • ± 30% ≤ 10 mg •± 35%