Medicated Feedingstuffs Regulations 1998 (No. 1046 of 1998).

These Regulations control the manufacture and distribution of medicated feedingstuffs. They provide for the approval (regs. 3 and 4), renewal of approval (reg. 5), late renewal (reg. 6) and withdrawal of approval (regulations 8 and 9) of premises for manufacturing medicated feedingstuffs. Regulations 10 to 16 also provide for a system of approval, renewal of approval and withdrawal of approval of distributors of medicated feedingstuffs. Regulation 17 covers the controls on agricultural merchants. Applications for approval, renewal of approval or late renewal of approval of premises or as distributor, subject to exceptions, must be accompanied by payment of such fee as specified in Schedule 1 (regs. 2 and 35). Regulations 19, 22 and 28 place record keeping requirements on persons engaged in the supply of medicated feedingstuffs and in the retail supply of products used to manufacture them. There are provisions controlling the manufacture, retail supply, packaging and labelling of particular products used to make medicated feedingstuffs (regs. 20, 21 and 23) and manufacture, packaging, labelling and supply of medicated feedingstuffs (regs. 24 to 28). Further controls are contained in regulations 29 to 34.