OpenLegislation

Paragraph 9 Additional record keeping requirements relating to veterinary medicinal productsI1

United Kingdom

(1)

Any person who—

(a)

incorporates a veterinary medicinal product into a premixture;

(b)

incorporates a premixture containing a veterinary medicinal product into feedingstuffs; or

(c)

incorporates a veterinary medicinal product into feedingstuffs,

  • must make a daily record of—

    1. (i)

      the types and quantities of all veterinary medicinal products (and specified feed additives, if any) and premixture used in the manufacturing process; and

    2. (ii)

      the quantity of feedingstuffs and premixture containing veterinary medicinal product manufactured that day.

(2)

An approved distributor must make a daily record of—

(a)

the types and quantities of all premixtures and feedingstuffs containing veterinary medicinal products bought and sold that day;

(b)

the quantity held.

(3)

A manufacturer and distributor must also record, as soon as reasonably practicable, for each consignment supplied—

(a)

the date of delivery;

(b)

the name and address of each consignee (or, in the case of a manufacturer supplying to a distributor, the name and address of the distributor);

(c)

the type of feedingstuffs or premixture supplied;

(d)

the quantity;

(e)

the type of veterinary medicinal product incorporated into the feedingstuffs; and

(f)

the expiry date.

(4)

Records must be kept for five years.

(5)

It is an offence to fail to comply with this paragraph.

Annotations

Commencement

I1

Sch. 5 para. 9 in force at 1.10.2006, see reg. 1