# The Veterinary Medicines Regulations 2013, Paragraph 11: Additional record keeping requirements relating to medicinal premixes

Extent: E+W+S

(1) Any person who—
(a) incorporates a medicinal premix into an intermediate feedingstuff;
(b) incorporates an intermediate feedingstuff containing a medicinal premix into feedingstuffs; or
(c) incorporates a medicinal premix into feedingstuffs,
must make a daily record of—
(d) the types and quantities of all medicinal premixes (and specified feed additives, if any) and intermediate feedingstuffs used in the manufacturing process; and
(e) the quantity of feedingstuffs and intermediate feedingstuffs containing medicinal premix manufactured that day.
(2) An authorised distributor must make a daily record of—
(a) the types and quantities of all intermediate feedingstuffs and feedingstuffs containing medicinal premixes bought and sold that day; and
(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 intermediate feedingstuffs supplied;
(d) the quantity;
(e) the type of medicinal premix incorporated into the feedingstuffs; ...
(f) the expiry date ; and
(g) the batch number.
(4) Records must be kept for five years.

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Source: https://www.legislation.gov.uk/uksi/2013/2033/schedule/5/paragraph/11 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2013/schedule-5/paragraph-11
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.