4 Amendments of Ulrike MÜLLER related to 2014/0255(COD)
Amendment 59 #
Proposal for a regulation
Recital 16
Recital 16
(16) Feed business operators manufacturing, whether they operate in a feed mill, with a specially equipped lorry or on-farm, storing, transporting or placing on the market medicated feed and intermediate products, should be approved by the competent authority, in line with the approval system laid down in Regulation (EC) No 183/2005, in order to ensure both feed safety and product traceability. Provision should be made for a transition procedure concerning establishments already approved under Directive 90/167/EEC. Establishments which administer medications to animals orally in the form of medicated feed should not be obliged to obtain an approval.
Amendment 84 #
Proposal for a regulation
Article 1 – paragraph 1 a (new)
Article 1 – paragraph 1 a (new)
This Regulation shall not apply to finished medicinal products to be orally administered that have been approved for use via feed or drinking water. Accordingly, the approval requirement set out in Recital 16 shall not apply to farms which use such medicinal products for their own herd.
Amendment 91 #
Proposal for a regulation
Article 1 – paragraph 1a (new)
Article 1 – paragraph 1a (new)
1a. This Regulation shall not apply to ready-prepared medications for oral administration which are approved for use in feedstuffs or drinking water, or to mixtures of such medications with feedstuffs which are manufactured for direct administration in livestock holdings.
Amendment 149 #
Proposal for a regulation
Article 4 – paragraph 1
Article 4 – paragraph 1
Feed business operators manufacturing, storing, transporting and placing on the market medicated feed and intermediate products shall put in place, implement and maintain a permanent written procedure or procedures based on the hazard analysis and critical control points (hereinafter: 'HACCP' ) system as provided for in Regulation (EC) No 183/2005. Mixtures consisting of feedstuffs and medications approved for oral use which are manufactured for immediate on-farm administration shall be exempt from the written procedure.